-
1
-
-
0000197885
-
The hemolytic effect of primaquine and related compounds. A review
-
Beutler E: The hemolytic effect of primaquine and related compounds. A review. Blood 14:103, 1959
-
(1959)
Blood
, vol.14
, pp. 103
-
-
Beutler, E.1
-
2
-
-
0000616920
-
Enzymatic deficiency in primaquine-sensitive erythrocytes
-
Carson PE, Flanagan CL, Ickes CE, Alving AS: Enzymatic deficiency in primaquine-sensitive erythrocytes. Science 124:484, 1956
-
(1956)
Science
, vol.124
, pp. 484
-
-
Carson, P.E.1
Flanagan, C.L.2
Ickes, C.E.3
Alving, A.S.4
-
3
-
-
0024414655
-
Congenital non-spherocytic haemolytic anaemias
-
Zanella A, Colombo MB, Rossi F, Merati G, Sirchia G: Congenital non-spherocytic haemolytic anaemias. Haernatologica 74:387, 1989
-
(1989)
Haernatologica
, vol.74
, pp. 387
-
-
Zanella, A.1
Colombo, M.B.2
Rossi, F.3
Merati, G.4
Sirchia, G.5
-
4
-
-
0002358651
-
Glucose-6-phosphate dehydrogenase deficiency and other enzyme abnormalities
-
Beutler E, Lichtman MA, Coller BS, Kipps TJ (eds): New York, NY, McGraw-Hill
-
Beutler E: Glucose-6-phosphate dehydrogenase deficiency and other enzyme abnormalities, in Beutler E, Lichtman MA, Coller BS, Kipps TJ (eds): Williams Hematology. New York, NY, McGraw-Hill, 1995, p 564
-
(1995)
Williams Hematology
, pp. 564
-
-
Beutler, E.1
-
5
-
-
0025176914
-
Erythroenzymopathies and hemolytic anemia: The many faces of inherited variant enzymes
-
Valentine WN, Paglia DE: Erythroenzymopathies and hemolytic anemia: The many faces of inherited variant enzymes. J Lab Clin Med 115:12, 1990
-
(1990)
J Lab Clin Med
, vol.115
, pp. 12
-
-
Valentine, W.N.1
Paglia, D.E.2
-
7
-
-
0022575528
-
Isolation of human glucose-6-phosphate dehydrogenase (G6PD) cDNA clones: Primary structure of the protein and unusual 5′ non-coding region
-
Persico MG, Viglietto G, Martino G, Toniolo D, Paonessa G, Moscatelli C, Dono R, Vulliamy T, Luzzatto L, D'Urso M: Isolation of human glucose-6-phosphate dehydrogenase (G6PD) cDNA clones: Primary structure of the protein and unusual 5′ non-coding region. Nucleic Acids Res 14:2511, 1986
-
(1986)
Nucleic Acids Res
, vol.14
, pp. 2511
-
-
Persico, M.G.1
Viglietto, G.2
Martino, G.3
Toniolo, D.4
Paonessa, G.5
Moscatelli, C.6
Dono, R.7
Vulliamy, T.8
Luzzatto, L.9
D'Urso, M.10
-
8
-
-
0022445321
-
Human glucose-6-phosphate dehydrogenase: Primary structure and cDNA cloning
-
Takizawa T, Huang IY, Ikuta T, Yoshida A: Human glucose-6-phosphate dehydrogenase: Primary structure and cDNA cloning. Proc Natl Acad Sci USA 83:4157, 1986
-
(1986)
Proc Natl Acad Sci USA
, vol.83
, pp. 4157
-
-
Takizawa, T.1
Huang, I.Y.2
Ikuta, T.3
Yoshida, A.4
-
9
-
-
0013669785
-
The red cell: A tiny dynamo
-
Wintrobe MM (ed): New York, NY, McGraw-Hill
-
Beutler E: The red cell: A tiny dynamo, in Wintrobe MM (ed): Blood Pure and Eloquent, New York, NY, McGraw-Hill, 1980, p 141
-
(1980)
Blood Pure and Eloquent
, pp. 141
-
-
Beutler, E.1
-
10
-
-
0000274748
-
The hemolytic effect of primaquine. II. The natural course of the hemolytic anemia and the mechanism of its self-limited character
-
Dem RJ, Beutler E, Alving AS: The hemolytic effect of primaquine. II. The natural course of the hemolytic anemia and the mechanism of its self-limited character. J Lab Clin Med 44:171, 1954
-
(1954)
J Lab Clin Med
, vol.44
, pp. 171
-
-
Dem, R.J.1
Beutler, E.2
Alving, A.S.3
-
11
-
-
84890444869
-
Denaturation of normal and abnormal erythrocytes II. Pathophysiology of hemolysis in glucose-6-phosphate dehydrogenase deficiency
-
Arese P, De Flora A: Denaturation of normal and abnormal erythrocytes II. Pathophysiology of hemolysis in glucose-6-phosphate dehydrogenase deficiency. Semin Hematol 27:1, 1990
-
(1990)
Semin Hematol
, vol.27
, pp. 1
-
-
Arese, P.1
De Flora, A.2
-
12
-
-
0021967304
-
Membrane cross bonding in red cells in favic crisis: A missing link in the mechanism of extravascular haemolysis
-
Fischer TM, Meloni T, Pescarmona GP, Arese P: Membrane cross bonding in red cells in favic crisis: A missing link in the mechanism of extravascular haemolysis. Br J Haematol 59:159, 1985
-
(1985)
Br J Haematol
, vol.59
, pp. 159
-
-
Fischer, T.M.1
Meloni, T.2
Pescarmona, G.P.3
Arese, P.4
-
13
-
-
0003486206
-
Standardization of procedures for the study of glucose-6-phosphate dehydrogenase
-
Report of a WHO scientific group. Serial No. 366
-
Betke K, Beutler E, Brewer GJ, Kirkman HN, Luzzatto L, Motulsky AG, Ramot B, Siniscalco M: Standardization of procedures for the study of glucose-6-phosphate dehydrogenase. Report of a WHO scientific group. WHO Technical Report, Serial No. 366, 1967
-
(1967)
WHO Technical Report
-
-
Betke, K.1
Beutler, E.2
Brewer, G.J.3
Kirkman, H.N.4
Luzzatto, L.5
Motulsky, A.G.6
Ramot, B.7
Siniscalco, M.8
-
14
-
-
0000274749
-
The hemolytic effect of primaquine. IV. The relationship of cell age to hemolysis
-
Beutler E, Dem RJ, Alving AS: The hemolytic effect of primaquine. IV. The relationship of cell age to hemolysis. J Lab Clin Med 44:439, 1954
-
(1954)
J Lab Clin Med
, vol.44
, pp. 439
-
-
Beutler, E.1
Dem, R.J.2
Alving, A.S.3
-
15
-
-
0014278261
-
In vivo lability of glucose-6-phosphate dehydrogenase in GdA-and Gd Mediterranean deficiency
-
Piomelli S, Corash LM, Davenport DD, Miraglia J, Amorosi EL: In vivo lability of glucose-6-phosphate dehydrogenase in GdA-and Gd Mediterranean deficiency. J Clin Invest 47:940, 1968
-
(1968)
J Clin Invest
, vol.47
, pp. 940
-
-
Piomelli, S.1
Corash, L.M.2
Davenport, D.D.3
Miraglia, J.4
Amorosi, E.L.5
-
16
-
-
33745950931
-
The course of experimentally-induced hemolytic anemia in a primaquine- sensitive Caucasian. A case study
-
Pannacciulli I, Tizianello A, Ajmar F, Salvidio E: The course of experimentally-induced hemolytic anemia in a primaquine- sensitive Caucasian. A case study. Blood 25:92, 1965
-
(1965)
Blood
, vol.25
, pp. 92
-
-
Pannacciulli, I.1
Tizianello, A.2
Ajmar, F.3
Salvidio, E.4
-
17
-
-
0014107015
-
Primaquine sensitivity in Caucasians: Hemolytic reactions induced by primaquine in G-6-PD deficient subjects
-
George JN, Sears DA, McCurdy P, Conrad ME: Primaquine sensitivity in Caucasians: Hemolytic reactions induced by primaquine in G-6-PD deficient subjects. J Lab Clin Med 70:80, 1967
-
(1967)
J Lab Clin Med
, vol.70
, pp. 80
-
-
George, J.N.1
Sears, D.A.2
McCurdy, P.3
Conrad, M.E.4
-
18
-
-
0001355596
-
The hemolytic effect of primaquine. V. Primaquine sensitivity as a manifestation of a multiple drug sensitivity
-
Dern RJ, Beutler E, Alving AS: The hemolytic effect of primaquine. V. Primaquine sensitivity as a manifestation of a multiple drug sensitivity. J Lab Clin Med 45:30, 1955
-
(1955)
J Lab Clin Med
, vol.45
, pp. 30
-
-
Dern, R.J.1
Beutler, E.2
Alving, A.S.3
-
20
-
-
0020076319
-
Influence of double genetic polymorphism on response to sulfamethazine
-
Woolhouse NM, Atu-Taylor LC: Influence of double genetic polymorphism on response to sulfamethazine. Clin Pharmacol Ther 31:377, 1982
-
(1982)
Clin Pharmacol Ther
, vol.31
, pp. 377
-
-
Woolhouse, N.M.1
Atu-Taylor, L.C.2
-
21
-
-
0019428954
-
Interactions of glucose-6-phosphate dehydrogenase deficiency with drug acetylation and hydroxylation reactions
-
Magon AM, Leipzig RM, Zannoni VG, Brewer GJ: Interactions of glucose-6-phosphate dehydrogenase deficiency with drug acetylation and hydroxylation reactions. J Lab Clin Med 97:764, 1981
-
(1981)
J Lab Clin Med
, vol.97
, pp. 764
-
-
Magon, A.M.1
Leipzig, R.M.2
Zannoni, V.G.3
Brewer, G.J.4
-
22
-
-
0007450684
-
Hemolytic effect of therapeutic drugs. Clinical considerations of the Primaquine-type hemolysis
-
Kellermeyer RW, Tarlov AR, Brewer GJ, Carson PE, Alving AS: Hemolytic effect of therapeutic drugs. Clinical considerations of the Primaquine-type hemolysis. JAMA 180:388, 1962
-
(1962)
JAMA
, vol.180
, pp. 388
-
-
Kellermeyer, R.W.1
Tarlov, A.R.2
Brewer, G.J.3
Carson, P.E.4
Alving, A.S.5
-
23
-
-
0016235599
-
Haemolytic effect of trimethoprim: Sulphamethoxazole in G-6-PD deficiency
-
Chan TK, McFadzean AJS: Haemolytic effect of trimethoprim: sulphamethoxazole in G-6-PD deficiency. Trans R Soc Trop Med Hyg 68:61, 1974
-
(1974)
Trans R Soc Trop Med Hyg
, vol.68
, pp. 61
-
-
Chan, T.K.1
McFadzean, A.J.S.2
-
24
-
-
0023297388
-
Use of trimethoprim-sulfamethoxazole in a glucose-6-phosphate dehydrogenase-deficient population
-
Markowitz N, Saravolatz LD: Use of trimethoprim-sulfamethoxazole in a glucose-6-phosphate dehydrogenase-deficient population. Rev Infect Dis 9:S218, 1987 (suppl 2)
-
(1987)
Rev Infect Dis
, vol.9
, Issue.2 SUPPL.
-
-
Markowitz, N.1
Saravolatz, L.D.2
-
25
-
-
1242314538
-
Haemolytic crisis after acetaminophen in glucose-6-phosphate dehydrogenase deficiency
-
Heintz B, Bock TA, Kierdorf H, Maurin N: Haemolytic crisis after acetaminophen in glucose-6-phosphate dehydrogenase deficiency. Klin Wochenschr 67:1068, 1989
-
(1989)
Klin Wochenschr
, vol.67
, pp. 1068
-
-
Heintz, B.1
Bock, T.A.2
Kierdorf, H.3
Maurin, N.4
-
26
-
-
0016357079
-
Red cell survival studies in glucose-6-phosphate dehydrogenase deficiency
-
Chan TK, Todd D, Tso SC: Red cell survival studies in glucose-6-phosphate dehydrogenase deficiency. Bull Hong Kong Med Assoc 26:41, 1974
-
(1974)
Bull Hong Kong Med Assoc
, vol.26
, pp. 41
-
-
Chan, T.K.1
Todd, D.2
Tso, S.C.3
-
27
-
-
0021741686
-
Acetaminophen and G-6-PD deficiency
-
Beutler E: Acetaminophen and G-6-PD deficiency. Acta Haematol 72:211, 1984
-
(1984)
Acta Haematol
, vol.72
, pp. 211
-
-
Beutler, E.1
-
28
-
-
17444449294
-
Hemolyse aigue par deficit en glucose 6 phosphate deshydrogenase au debut du traitement d'un myelome role du melphalan
-
Casassus P, Vannetzel JM, Lortholary P: Hemolyse aigue par deficit en glucose 6 phosphate deshydrogenase au debut du traitement d'un myelome role du melphalan. Nouv Presse Med 11:2296, 1982
-
(1982)
Nouv Presse Med
, vol.11
, pp. 2296
-
-
Casassus, P.1
Vannetzel, J.M.2
Lortholary, P.3
-
29
-
-
0018139677
-
Hemolysis during BAL chelation therapy for high blood lead levels in two G 6 PD deficient children
-
Janakiraman N, Seeler RA, Royal JE, Chen MF: Hemolysis during BAL chelation therapy for high blood lead levels in two G 6 PD deficient children. Clin Pediatr 17:485, 1978
-
(1978)
Clin Pediatr
, vol.17
, pp. 485
-
-
Janakiraman, N.1
Seeler, R.A.2
Royal, J.E.3
Chen, M.F.4
-
30
-
-
0020624338
-
Oxidative haemolysis after administration of doxorubicin
-
Doll DC: Oxidative haemolysis after administration of doxorubicin. BMJ 287:180, 1983
-
(1983)
BMJ
, vol.287
, pp. 180
-
-
Doll, D.C.1
-
31
-
-
85060264240
-
Durch Neo-salvarsan ausgelöste Hämolyse bei Glukose-6-phosphat-dehydrogenase-mangel, kombiniert mit hepatischem Icterus
-
Michot F, Rastetter J, Gronauer H: Durch Neo-salvarsan ausgelöste Hämolyse bei Glukose-6-phosphat-dehydrogenase-mangel, kombiniert mit hepatischem Icterus. Schweiz Med Wochenschr 96:985, 1966
-
(1966)
Schweiz Med Wochenschr
, vol.96
, pp. 985
-
-
Michot, F.1
Rastetter, J.2
Gronauer, H.3
-
33
-
-
0013909147
-
On the familial predisposition to favism
-
Stamatoyannopoulos G, Fraser GR, Motulsky AG, Fessas P, Akrivakis A, Papayannopoulou T: On the familial predisposition to favism. Am J Hum Genet 18:253, 1966
-
(1966)
Am J Hum Genet
, vol.18
, pp. 253
-
-
Stamatoyannopoulos, G.1
Fraser, G.R.2
Motulsky, A.G.3
Fessas, P.4
Akrivakis, A.5
Papayannopoulou, T.6
-
34
-
-
0024564677
-
Glucose-6-phosphate dehydrogenase (G6PD) deficiency in southern Italy: A case of G6PD A(-) associated with favism
-
Calabr̀o V, Cascone A, Malaspina P, Battistuzzi G: Glucose-6-phosphate dehydrogenase (G6PD) deficiency in southern Italy: A case of G6PD A(-) associated with favism. Haematologica 74:71, 1989
-
(1989)
Haematologica
, vol.74
, pp. 71
-
-
Calabr̀o, V.1
Cascone, A.2
Malaspina, P.3
Battistuzzi, G.4
-
35
-
-
0025121962
-
-)
-
-). BMJ 300:236, 1990
-
(1990)
BMJ
, vol.300
, pp. 236
-
-
Galiano, S.1
Gaetani, G.F.2
Barabino, A.3
Cottafava, F.4
Zeitlin, H.5
Town, M.6
Luzzatto, L.7
-
37
-
-
0000182614
-
The hemolytic effect of primaquine. III. A study of primaquine-sensitive erythrocytes
-
Beutler E, Dern RJ, Alving AS: The hemolytic effect of primaquine. III. A study of primaquine-sensitive erythrocytes. J Lab Clin Med 44:177, 1954
-
(1954)
J Lab Clin Med
, vol.44
, pp. 177
-
-
Beutler, E.1
Dern, R.J.2
Alving, A.S.3
-
38
-
-
0018643565
-
Generation of hydroxyl radical by enzymes, chemicals, and human phagocytes in vitro
-
Repine JE, Eaton JW, Anders MW, Hoidal JR, Fox RB: Generation of hydroxyl radical by enzymes, chemicals, and human phagocytes in vitro. J Clin Invest 64:1642, 1979
-
(1979)
J Clin Invest
, vol.64
, pp. 1642
-
-
Repine, J.E.1
Eaton, J.W.2
Anders, M.W.3
Hoidal, J.R.4
Fox, R.B.5
-
39
-
-
0024554253
-
Ascorbate-induced generation of free radical species in normal and glucose-6-phosphate dehydrogenase-deficient erythrocytes
-
Rakitzis ET, Papandreou PT: Ascorbate-induced generation of free radical species in normal and glucose-6-phosphate dehydrogenase-deficient erythrocytes. Biochem Soc Trans 17:371, 1989
-
(1989)
Biochem Soc Trans
, vol.17
, pp. 371
-
-
Rakitzis, E.T.1
Papandreou, P.T.2
-
40
-
-
0024203361
-
Oxidative hemolysis of erythrocytes and its inhibition by free radical scavengers
-
Niki E, Komuro E, Takahashi M, Urano S, Ito E, Terao K: Oxidative hemolysis of erythrocytes and its inhibition by free radical scavengers. J Biol Chem 263:19809, 1988
-
(1988)
J Biol Chem
, vol.263
, pp. 19809
-
-
Niki, E.1
Komuro, E.2
Takahashi, M.3
Urano, S.4
Ito, E.5
Terao, K.6
-
41
-
-
0024422228
-
Oxidative stress: A radical view
-
Saltman P: Oxidative stress: A radical view. Semin Hematol 26:249, 1989
-
(1989)
Semin Hematol
, vol.26
, pp. 249
-
-
Saltman, P.1
-
42
-
-
0025855112
-
Ascorbate- and dehydroascorbic acid-mediated reduction of free radicals in the human erythrocyte
-
Mehlhorn RJ: Ascorbate- and dehydroascorbic acid-mediated reduction of free radicals in the human erythrocyte. J Biol Chem 266:2724, 1991
-
(1991)
J Biol Chem
, vol.266
, pp. 2724
-
-
Mehlhorn, R.J.1
-
43
-
-
0023655258
-
Oxygen radicals stimulate intracellular proteolysis and lipid peroxidation by independent mechanisms in erythrocytes
-
Davies KJA, Goldberg AL: Oxygen radicals stimulate intracellular proteolysis and lipid peroxidation by independent mechanisms in erythrocytes. J Biol Chem 262:8220, 1987
-
(1987)
J Biol Chem
, vol.262
, pp. 8220
-
-
Davies, K.J.A.1
Goldberg, A.L.2
-
44
-
-
0024272721
-
Perspectives on hydrogen peroxide and druginduced hemolytic anemia in glucose-6-phosphate dehydrogenase deficiency
-
Hochstein P: Perspectives on hydrogen peroxide and druginduced hemolytic anemia in glucose-6-phosphate dehydrogenase deficiency. J Free Radical Biol Med 5:387, 1988
-
(1988)
J Free Radical Biol Med
, vol.5
, pp. 387
-
-
Hochstein, P.1
-
45
-
-
0017288716
-
Haemolytic effect of two sulphonamides evaluated by a new method
-
Gaetani GD, Mareni C, Ravazzolo R, Salvidio E: Haemolytic effect of two sulphonamides evaluated by a new method. Br J Haematol 32:183, 1976
-
(1976)
Br J Haematol
, vol.32
, pp. 183
-
-
Gaetani, G.D.1
Mareni, C.2
Ravazzolo, R.3
Salvidio, E.4
-
46
-
-
0023855516
-
Attempts to predict the hemolytic potential of drugs in glucose-6-phosphate dehydrogenase deficiency of the Mediterranean type by an in vitro test
-
Bashan N, Peleg N, Moses SW: Attempts to predict the hemolytic potential of drugs in glucose-6-phosphate dehydrogenase deficiency of the Mediterranean type by an in vitro test. Isr J Med Sci 24:61, 1988
-
(1988)
Isr J Med Sci
, vol.24
, pp. 61
-
-
Bashan, N.1
Peleg, N.2
Moses, S.W.3
-
47
-
-
0020557887
-
Microsomal incubation test of potentially hemolytic drugs for glucose-6-phosphate dehydrogenase deficiency
-
Bloom KE, Brewer GJ, Magon AM, Wetterstroem N: Microsomal incubation test of potentially hemolytic drugs for glucose-6-phosphate dehydrogenase deficiency. Clin Pharmacol Ther 33:403, 1983
-
(1983)
Clin Pharmacol Ther
, vol.33
, pp. 403
-
-
Bloom, K.E.1
Brewer, G.J.2
Magon, A.M.3
Wetterstroem, N.4
-
48
-
-
0023880325
-
Tolerability of tiaprofenic acid in patients with glucose-6-phosphate dehydrogenase (G6PD) deficiency
-
Mela Q, Perpignano G, Ruggiero V, Longatti S: Tolerability of tiaprofenic acid in patients with glucose-6-phosphate dehydrogenase (G6PD) deficiency. Drugs 35:107, 1988
-
(1988)
Drugs
, vol.35
, pp. 107
-
-
Mela, Q.1
Perpignano, G.2
Ruggiero, V.3
Longatti, S.4
-
49
-
-
0014285106
-
Low erythrocyte glucose-6-phosphate dehydrogenase activity and primaquine insensitivity in sheep
-
Smith JE: Low erythrocyte glucose-6-phosphate dehydrogenase activity and primaquine insensitivity in sheep. J Lab Clin Med 71:826, 1968
-
(1968)
J Lab Clin Med
, vol.71
, pp. 826
-
-
Smith, J.E.1
-
50
-
-
0022870305
-
Predictive models for human glucose-6-phosphate dehydrogenase deficiency
-
Horton HM, Calabrese EJ: Predictive models for human glucose-6-phosphate dehydrogenase deficiency. Drug Metab Rev 17:261, 1986
-
(1986)
Drug Metab Rev
, vol.17
, pp. 261
-
-
Horton, H.M.1
Calabrese, E.J.2
-
51
-
-
0017116721
-
Glucose-6-phosphate dehydrogenase deficiency in a dog
-
Smith JE, Ryer K, Wallace L: Glucose-6-phosphate dehydrogenase deficiency in a dog. Enzyme 21:379, 1976
-
(1976)
Enzyme
, vol.21
, pp. 379
-
-
Smith, J.E.1
Ryer, K.2
Wallace, L.3
-
52
-
-
0023957185
-
X-linked glucose-6-phosphate dehydrogenase deficiency in Mus musculus
-
Pretsch W, Charles DJ, Merkle S: X-linked glucose-6-phosphate dehydrogenase deficiency in Mus musculus. Biochem Genet 26:89, 1988
-
(1988)
Biochem Genet
, vol.26
, pp. 89
-
-
Pretsch, W.1
Charles, D.J.2
Merkle, S.3
-
53
-
-
0014069294
-
Vererbbarer Glucose-6-phosphatdehydrogenasemangel in den Erythrocyten von Ratten
-
Werth G, Mueller G: Vererbbarer Glucose-6-phosphatdehydrogenasemangel in den Erythrocyten von Ratten. Klin Wochenschr 45:265, 1967
-
(1967)
Klin Wochenschr
, vol.45
, pp. 265
-
-
Werth, G.1
Mueller, G.2
-
54
-
-
4243257281
-
A mouse mutant deficient in erythrocyte glucose-6-phosphate dehydrogenase after paternal ethylnitrosourea treatment
-
Charles DJ, Pretsch W: A mouse mutant deficient in erythrocyte glucose-6-phosphate dehydrogenase after paternal ethylnitrosourea treatment. Genetics 107:S19 1984 (suppl)
-
(1984)
Genetics
, vol.107
, Issue.SUPPL.
-
-
Charles, D.J.1
Pretsch, W.2
-
55
-
-
1242314541
-
Studies on erythrocytes in cases with past history of favism and drug-induced acute hemolytic anemia
-
Szeinberg A, Sheba C, Hirshorn N, Bodonyi E: Studies on erythrocytes in cases with past history of favism and drug-induced acute hemolytic anemia. Blood 12:603, 1957
-
(1957)
Blood
, vol.12
, pp. 603
-
-
Szeinberg, A.1
Sheba, C.2
Hirshorn, N.3
Bodonyi, E.4
-
56
-
-
70449174023
-
Studies on glutathione stability in erythrocytes of cases with past history of favism or sulfadrug-induced hemolysis
-
Szeinberg A, Asher Y, Sheba C: Studies on glutathione stability in erythrocytes of cases with past history of favism or sulfadrug-induced hemolysis. Blood 13:348, 1958
-
(1958)
Blood
, vol.13
, pp. 348
-
-
Szeinberg, A.1
Asher, Y.2
Sheba, C.3
-
57
-
-
0004656072
-
Glucose-6-phosphate dehydrogenase deficiency
-
Doxiadis SA, Fessas P, Valaes T, Mastrokalos N: Glucose-6-phosphate dehydrogenase deficiency. Lancet 1:297, 1961
-
(1961)
Lancet
, vol.1
, pp. 297
-
-
Doxiadis, S.A.1
Fessas, P.2
Valaes, T.3
Mastrokalos, N.4
-
58
-
-
75449126883
-
Chloramphenicol induced haemolytic anaemia due to enzymatic deficiency of erythrocytes
-
Chatterji SC, Das PK: Chloramphenicol induced haemolytic anaemia due to enzymatic deficiency of erythrocytes. J Indian Med Assoc 40:172, 1963
-
(1963)
J Indian Med Assoc
, vol.40
, pp. 172
-
-
Chatterji, S.C.1
Das, P.K.2
-
59
-
-
78651167610
-
Clinical manifestations of primaquine-sensitive anemia
-
Berry DH, Vietti TJ: Clinical manifestations of primaquine-sensitive anemia. Am J Dis Child 110:166, 1965
-
(1965)
Am J Dis Child
, vol.110
, pp. 166
-
-
Berry, D.H.1
Vietti, T.J.2
-
60
-
-
3142526035
-
Viral hepatitis in G-6-PD deficiency
-
Boon WH: Viral hepatitis in G-6-PD deficiency. Lancet 1:882, 1966
-
(1966)
Lancet
, vol.1
, pp. 882
-
-
Boon, W.H.1
-
61
-
-
0000681746
-
Clinical spectrum of hemolytic anemia associated with G 6 PD deficiency
-
Burka ER, Weaver III Z, Marks PA: Clinical spectrum of hemolytic anemia associated with G 6 PD deficiency. Ann Intern Med 64:817, 1966
-
(1966)
Ann Intern Med
, vol.64
, pp. 817
-
-
Burka, E.R.1
Weaver III, Z.2
Marks, P.A.3
-
62
-
-
0013985997
-
Acute hemolytic anemia complicating viral hepatitis in patients with glucose-6-phosphate dehydrogenase deficiency
-
Salen G, Goldstein F, Haurani F, Wirts CW: Acute hemolytic anemia complicating viral hepatitis in patients with glucose-6-phosphate dehydrogenase deficiency. Ann Intern Med 65:1210, 1966
-
(1966)
Ann Intern Med
, vol.65
, pp. 1210
-
-
Salen, G.1
Goldstein, F.2
Haurani, F.3
Wirts, C.W.4
-
63
-
-
0014219056
-
Haemolysis in typhoid fever in children with G-6-PD deficiency
-
Hersko C, Vardy PA: Haemolysis in typhoid fever in children with G-6-PD deficiency. BMJ 1:214, 1967
-
(1967)
BMJ
, vol.1
, pp. 214
-
-
Hersko, C.1
Vardy, P.A.2
-
64
-
-
0014067381
-
Anemia during acute infections. Role of glucose-6-phosphate dehydrogenase deficiency in negroes
-
Mengel CE, Metz E, Yancey WS: Anemia during acute infections. Role of glucose-6-phosphate dehydrogenase deficiency in negroes. Arch Intern Med 119:287, 1967
-
(1967)
Arch Intern Med
, vol.119
, pp. 287
-
-
Mengel, C.E.1
Metz, E.2
Yancey, W.S.3
-
65
-
-
0014280223
-
Anemia emolitica acuta in corso di sepsi da proteus morganii in soggetto carente di glucoso - 6 - fosfato deidrogenasi eritrocitaria
-
Arcuri F, Robert L: Anemia emolitica acuta in corso di sepsi da proteus morganii in soggetto carente di glucoso - 6 - fosfato deidrogenasi eritrocitaria. Arch E Maragliano Patol Clin 24:347, 1968
-
(1968)
Arch e Maragliano Patol Clin
, vol.24
, pp. 347
-
-
Arcuri, F.1
Robert, L.2
-
66
-
-
0014318657
-
Acute renal failure complicating rickettsial infections in glucose-6-phosphate dehydrogenase-deficient individuals
-
Whelton A, Donadio JVJ, Elisberg BL: Acute renal failure complicating rickettsial infections in glucose-6-phosphate dehydrogenase-deficient individuals. Ann Intern Med 69:323, 1968
-
(1968)
Ann Intern Med
, vol.69
, pp. 323
-
-
Whelton, A.1
Donadio, J.V.J.2
Elisberg, B.L.3
-
67
-
-
85060261416
-
Incidence of hemolysis in acute infections among G-6-PD deficient children
-
Abrahamov A, Freier S, Goldstein R: Incidence of hemolysis in acute infections among G-6-PD deficient children. Harefuah 77:180, 1969
-
(1969)
Harefuah
, vol.77
, pp. 180
-
-
Abrahamov, A.1
Freier, S.2
Goldstein, R.3
-
68
-
-
85060263422
-
Anemia emolitica acuta in corso di sepsi da proteus morganii in soggetto carente di glucosio-6-fosfato deidrogenasi eritocitaria
-
Arcuri F, Robert L: Anemia emolitica acuta in corso di sepsi da proteus morganii in soggetto carente di glucosio-6-fosfato deidrogenasi eritocitaria. Giornale de Malattie Infettive 21:257, 1969
-
(1969)
Giornale de Malattie Infettive
, vol.21
, pp. 257
-
-
Arcuri, F.1
Robert, L.2
-
69
-
-
0005965057
-
Acute viral hepatitis, glucose-6-phosphate dehydrogenase deficiency, and hemolytic anemia
-
Clearfield HR, Brody JI, Tumen HJ: Acute viral hepatitis, glucose-6-phosphate dehydrogenase deficiency, and hemolytic anemia. Arch Intern Med 123:689, 1969
-
(1969)
Arch Intern Med
, vol.123
, pp. 689
-
-
Clearfield, H.R.1
Brody, J.I.2
Tumen, H.J.3
-
70
-
-
0014442771
-
Glucose-6-phosphate dehydrogenase deficiency, infectious hepatitis, acute hemolysis, and renal failure
-
Phillips SM, Silvers NP: Glucose-6-phosphate dehydrogenase deficiency, infectious hepatitis, acute hemolysis, and renal failure. Ann Intern Med 70:99, 1969
-
(1969)
Ann Intern Med
, vol.70
, pp. 99
-
-
Phillips, S.M.1
Silvers, N.P.2
-
71
-
-
0014842217
-
The hemolytic process of viral hepatitis in children with normal or deficient glucose-6-phosphate dehydrogenase activity
-
Kattamis CA, Tjortjatou F: The hemolytic process of viral hepatitis in children with normal or deficient glucose-6-phosphate dehydrogenase activity. J Pediatr 77:422, 1970
-
(1970)
J Pediatr
, vol.77
, pp. 422
-
-
Kattamis, C.A.1
Tjortjatou, F.2
-
72
-
-
0015175120
-
Oxidant injury of Caucasian glucose-6-phosphate dehydrogenase-deficient red blood cells by phagocytosing leukocytes during infection
-
Baehner RL, Nathan DG, Castle WB: Oxidant injury of Caucasian glucose-6-phosphate dehydrogenase-deficient red blood cells by phagocytosing leukocytes during infection. J Clin Invest 50:2466, 1971
-
(1971)
J Clin Invest
, vol.50
, pp. 2466
-
-
Baehner, R.L.1
Nathan, D.G.2
Castle, W.B.3
-
73
-
-
0015012562
-
The survival of glucose-6-phosphate dehydrogenase-deficient erythrocytes in patients with typhoid fever on chloramphenicol therapy
-
Chan TK, Chesterman CN, McFadzean AJS, Todd D: The survival of glucose-6-phosphate dehydrogenase-deficient erythrocytes in patients with typhoid fever on chloramphenicol therapy. J Lab Clin Med 77:177, 1971
-
(1971)
J Lab Clin Med
, vol.77
, pp. 177
-
-
Chan, T.K.1
Chesterman, C.N.2
McFadzean, A.J.S.3
Todd, D.4
-
74
-
-
0015379444
-
Acute haemolytic anaemia in typhoid fever
-
Bakshi S, Singh J: Acute haemolytic anaemia in typhoid fever. Indian J Pediatr 39:270, 1972
-
(1972)
Indian J Pediatr
, vol.39
, pp. 270
-
-
Bakshi, S.1
Singh, J.2
-
75
-
-
0015499683
-
G-6-PD deficiency, typhoid, and co-trimoxazole
-
Chan TK: G-6-PD deficiency, typhoid, and co-trimoxazole. Lancet 2:1258, 1972
-
(1972)
Lancet
, vol.2
, pp. 1258
-
-
Chan, T.K.1
-
76
-
-
0015497166
-
Insuffisance renale aigue. Revelatrice d'un deficit en glucose-6-phosphate deshydrogenase: Gravite de l'hemolyse istrogene
-
Larcan A, Kaiffer M, Maitrehanche M, Genetet B, Vigneron C: Insuffisance renale aigue. Revelatrice d'un deficit en glucose-6-phosphate deshydrogenase: Gravite de l'hemolyse istrogene. Nouv Presse Med 35:2299, 1972
-
(1972)
Nouv Presse Med
, vol.35
, pp. 2299
-
-
Larcan, A.1
Kaiffer, M.2
Maitrehanche, M.3
Genetet, B.4
Vigneron, C.5
-
77
-
-
0016772497
-
Glucose-6-phosphate dehydrogenase deficiency in Thai children with typhoid fever
-
Lampe RM, Kirdpon S, Mansuwan P, Benenson MW: Glucose-6-phosphate dehydrogenase deficiency in Thai children with typhoid fever. J Pediatr 87:576, 1975
-
(1975)
J Pediatr
, vol.87
, pp. 576
-
-
Lampe, R.M.1
Kirdpon, S.2
Mansuwan, P.3
Benenson, M.W.4
-
79
-
-
0017755599
-
Combined G-6PD and 6-PGD deficiency in a Hindu boy
-
Dash S, Bhagwat AG: Combined G-6PD and 6-PGD deficiency in a Hindu boy. Acta Haematol 57:351, 1977
-
(1977)
Acta Haematol
, vol.57
, pp. 351
-
-
Dash, S.1
Bhagwat, A.G.2
-
80
-
-
0018411989
-
Crisi emolitica da deficit di G-6-PD in corso di epatite virale di tipo a
-
Veglio V, Gaiottino F: Crisi emolitica da deficit di G-6-PD in corso di epatite virale di tipo a. Minerva Med 70:357, 1979
-
(1979)
Minerva Med
, vol.70
, pp. 357
-
-
Veglio, V.1
Gaiottino, F.2
-
81
-
-
0019946554
-
Severe hemolytic anemia in black children with glucose-6-phosphate dehydrogenase deficiency
-
Shannon K, Buchanan GR: Severe hemolytic anemia in black children with glucose-6-phosphate dehydrogenase deficiency. Pediatrics 70:364, 1982
-
(1982)
Pediatrics
, vol.70
, pp. 364
-
-
Shannon, K.1
Buchanan, G.R.2
-
82
-
-
0020054476
-
Severe glucose-6-phosphate dehydrogenase (G 6 PD) deficiency associated with chronic hemolytic anemia, granulocyte dysfunction, and increased susceptibility to infections. Description of a new molecular variant (G 6 PD Barcelona)
-
Vives-Corrons JL, Feliu E, Pujades MA, Rozman C, Carreras A, Vallespi MT: Severe glucose-6-phosphate dehydrogenase (G 6 PD) deficiency associated with chronic hemolytic anemia, granulocyte dysfunction, and increased susceptibility to infections. Description of a new molecular variant (G 6 PD Barcelona). Blood 59:428, 1982
-
(1982)
Blood
, vol.59
, pp. 428
-
-
Vives-Corrons, J.L.1
Feliu, E.2
Pujades, M.A.3
Rozman, C.4
Carreras, A.5
Vallespi, M.T.6
-
84
-
-
0022254743
-
Cytomegalovirus infection and hemolytic anemia due to glucose-6-phosphate dehydrogenase deficiency
-
Rosenbloom BE, Rosenfelt FP, Ullman H, Weinstein IM: Cytomegalovirus infection and hemolytic anemia due to glucose-6-phosphate dehydrogenase deficiency. Mt Sinai J Med 52:363, 1985
-
(1985)
Mt Sinai J Med
, vol.52
, pp. 363
-
-
Rosenbloom, B.E.1
Rosenfelt, F.P.2
Ullman, H.3
Weinstein, I.M.4
-
85
-
-
0022650563
-
G6PD-deticiency infectious haemolysis: A complement dependent innocent bystander phenomenon
-
Kasper ML, Miller WJ, Jacob HS: G6PD-deticiency infectious haemolysis: a complement dependent innocent bystander phenomenon. Br J Haematol 63:85, 1986
-
(1986)
Br J Haematol
, vol.63
, pp. 85
-
-
Kasper, M.L.1
Miller, W.J.2
Jacob, H.S.3
-
86
-
-
0022832153
-
Haemolysis with Mediterranean spotted fever and glucose6-phosphate dehydrogenase deficiency
-
Raoult D, Lena D, Perrimont H, Gallais H, Walker DH, Casanova P: Haemolysis with Mediterranean spotted fever and glucose6-phosphate dehydrogenase deficiency. Trans R Soc Trop Med Hyg 80:961, 1986
-
(1986)
Trans R Soc Trop Med Hyg
, vol.80
, pp. 961
-
-
Raoult, D.1
Lena, D.2
Perrimont, H.3
Gallais, H.4
Walker, D.H.5
Casanova, P.6
-
87
-
-
0023757257
-
Severe hemolytic anemia due to glucose-6-phosphate dehydrogenase deficiency and Epstein-Barr virus infection
-
Rosenbloom BE, Weingarten S, Rosenfelt FP, Weinstein IM: Severe hemolytic anemia due to glucose-6-phosphate dehydrogenase deficiency and Epstein-Barr virus infection. Mt Sinai J Med 55:404, 1988
-
(1988)
Mt Sinai J Med
, vol.55
, pp. 404
-
-
Rosenbloom, B.E.1
Weingarten, S.2
Rosenfelt, F.P.3
Weinstein, I.M.4
-
88
-
-
0025829894
-
Glucose-6-phosphate dehydrogenase deficiency and bacterial infections in northern Sardinia
-
Meloni T, Forteleoni G, Ena F, Meloni GF: Glucose-6-phosphate dehydrogenase deficiency and bacterial infections in northern Sardinia. J Pediatr 118:909, 1991
-
(1991)
J Pediatr
, vol.118
, pp. 909
-
-
Meloni, T.1
Forteleoni, G.2
Ena, F.3
Meloni, G.F.4
-
89
-
-
0028287096
-
Nitric oxide reacts with intracellular glutathione and activates the hexose monophosphate shunt in human neutrophils: Evidence for 5-nitrosoglutathione as a bioactive intermediary
-
Clancy RM, Levartovsky D, Leszczynska-Piziak J, Yegudin J, Abramson SB: Nitric oxide reacts with intracellular glutathione and activates the hexose monophosphate shunt in human neutrophils: Evidence for 5-nitrosoglutathione as a bioactive intermediary. Proc Natl Acad Sci USA 91:3680, 1994
-
(1994)
Proc Natl Acad Sci USA
, vol.91
, pp. 3680
-
-
Clancy, R.M.1
Levartovsky, D.2
Leszczynska-Piziak, J.3
Yegudin, J.4
Abramson, S.B.5
-
90
-
-
0015351557
-
G-6-PD hemolytic anemia complicating diabetic ketoacidosis
-
Gellady A, Greenwood RD: G-6-PD hemolytic anemia complicating diabetic ketoacidosis. J Pediatr 80:1037, 1972
-
(1972)
J Pediatr
, vol.80
, pp. 1037
-
-
Gellady, A.1
Greenwood, R.D.2
-
91
-
-
0021266621
-
Diabetic ketoacidosis does not precipitate haemolysis in patients with the Mediterranean variant of glucose-6-phosphate dehydrogenase deficiency
-
Shalev O, Wollner A, Menczel J: Diabetic ketoacidosis does not precipitate haemolysis in patients with the Mediterranean variant of glucose-6-phosphate dehydrogenase deficiency. BMJ 288:179, 1984
-
(1984)
BMJ
, vol.288
, pp. 179
-
-
Shalev, O.1
Wollner, A.2
Menczel, J.3
-
92
-
-
0022234813
-
Hypoglycemia-induced hemolysis in glucose-6-phosphate dehydrogenase deficiency
-
Shalev O, Eliakim R, Lugassy GZ, Menczel J: Hypoglycemia-induced hemolysis in glucose-6-phosphate dehydrogenase deficiency. Acta Haematol 74:227, 1985
-
(1985)
Acta Haematol
, vol.74
, pp. 227
-
-
Shalev, O.1
Eliakim, R.2
Lugassy, G.Z.3
Menczel, J.4
-
93
-
-
0013357868
-
Glutathione sensitive chronic nonspherocytic hemolytic anemia
-
Newton WAJ, Bass JC: Glutathione sensitive chronic nonspherocytic hemolytic anemia. Am J Dis Child 96:501, 1958
-
(1958)
Am J Dis Child
, vol.96
, pp. 501
-
-
Newton, W.A.J.1
Bass, J.C.2
-
94
-
-
0003677971
-
Chronic hemolysis associated with glucose-6-phosphate deficiency
-
Ben-Ishay D, Izak G: Chronic hemolysis associated with glucose-6-phosphate deficiency. J Lab Clin Med 63:1002, 1964
-
(1964)
J Lab Clin Med
, vol.63
, pp. 1002
-
-
Ben-Ishay, D.1
Izak, G.2
-
95
-
-
0014247508
-
Biochemical variants of glucose-6-phosphate dehydrogenase giving rise to congenital nonspherocytic hemolytic disease
-
Beutler E, Mathai CK, Smith JE: Biochemical variants of glucose-6-phosphate dehydrogenase giving rise to congenital nonspherocytic hemolytic disease. Blood 31:131, 1968
-
(1968)
Blood
, vol.31
, pp. 131
-
-
Beutler, E.1
Mathai, C.K.2
Smith, J.E.3
-
96
-
-
0027512086
-
G6PD "Campinas:" A deficient enzyme with a mutation at the far 3′ end of the gene
-
Baronciani L, Tricta F, Beutler E: G6PD "Campinas:" A deficient enzyme with a mutation at the far 3′ end of the gene. Hum Mutat 2:77, 1993
-
(1993)
Hum Mutat
, vol.2
, pp. 77
-
-
Baronciani, L.1
Tricta, F.2
Beutler, E.3
-
97
-
-
0014816612
-
G-6-PD Tripler: A unique variant associated with chronic hemolytic disease
-
Engstrom PF, Beutler E: G-6-PD Tripler: A unique variant associated with chronic hemolytic disease. Blood 36:10, 1970
-
(1970)
Blood
, vol.36
, pp. 10
-
-
Engstrom, P.F.1
Beutler, E.2
-
98
-
-
0015918157
-
Hemolytic anemia and G-6-PD deficiency
-
Yoshida A: Hemolytic anemia and G-6-PD deficiency. Science 179:532, 1973
-
(1973)
Science
, vol.179
, pp. 532
-
-
Yoshida, A.1
-
99
-
-
0015109643
-
G6PD deficiency and chronic hemolysis: Four new mutants - Relationships between clinical syndrome and enzyme kinetics
-
Rattazzi MC, Corash LM, Van Zanen GE, Jaffe ER, Piomelli S: G6PD deficiency and chronic hemolysis: Four new mutants - Relationships between clinical syndrome and enzyme kinetics. Blood 38:205, 1971
-
(1971)
Blood
, vol.38
, pp. 205
-
-
Rattazzi, M.C.1
Corash, L.M.2
Van Zanen, G.E.3
Jaffe, E.R.4
Piomelli, S.5
-
100
-
-
0018710778
-
Glucose-6-phosphate dehydrogenase deficiency and neonatal jaundice in Jamaica
-
Gibbs WN, Gray R, Lowry M: Glucose-6-phosphate dehydrogenase deficiency and neonatal jaundice in Jamaica. Br J Haematol 43:263, 1979
-
(1979)
Br J Haematol
, vol.43
, pp. 263
-
-
Gibbs, W.N.1
Gray, R.2
Lowry, M.3
-
101
-
-
0014300842
-
Hyperbilirubinemia and kernicterus in glucose-6-phosphate dehydrogenase-deficient infants in Singapore
-
Brown WR, Boon WH: Hyperbilirubinemia and kernicterus in glucose-6-phosphate dehydrogenase-deficient infants in Singapore. Pediatrics 41:1055, 1968
-
(1968)
Pediatrics
, vol.41
, pp. 1055
-
-
Brown, W.R.1
Boon, W.H.2
-
102
-
-
15844397689
-
Su due casi di ittero nucleare in neonati con difetto enzimatico eritrocitario
-
Segni G: Su due casi di ittero nucleare in neonati con difetto enzimatico eritrocitario. Minerva Pediatr 11:1420, 1959
-
(1959)
Minerva Pediatr
, vol.11
, pp. 1420
-
-
Segni, G.1
-
104
-
-
0015634270
-
Phenobarbital for prevention of hyperbilirubinemia in glucose-6-phosphate dehydrogenase deficient newborn infants
-
Meloni T, Cagnazzo G, Dore A, Cutillo S: Phenobarbital for prevention of hyperbilirubinemia in glucose-6-phosphate dehydrogenase deficient newborn infants. J Pediatr 82:1048, 1973
-
(1973)
J Pediatr
, vol.82
, pp. 1048
-
-
Meloni, T.1
Cagnazzo, G.2
Dore, A.3
Cutillo, S.4
-
105
-
-
0028362766
-
Severe neonatal jaundice associated with glucose-6-phosphate dehydrogenase deficiency: Pathogenesis and global epidemiology
-
Valaes T: Severe neonatal jaundice associated with glucose-6-phosphate dehydrogenase deficiency: Pathogenesis and global epidemiology. Acta Paediatr 83:58, 1994 (suppl 394)
-
(1994)
Acta Paediatr
, vol.83
, Issue.394 SUPPL.
, pp. 58
-
-
Valaes, T.1
-
106
-
-
0019782212
-
Glucose-6-phosphate dehydrogenase status and neonatal jaundice
-
Tan KL: Glucose-6-phosphate dehydrogenase status and neonatal jaundice. Arch Dis Child 56:874, 1981
-
(1981)
Arch Dis Child
, vol.56
, pp. 874
-
-
Tan, K.L.1
-
107
-
-
0019125410
-
Singapore kernicterus
-
Boon WH: Singapore kernicterus. Singapore Med J 21:556, 1980
-
(1980)
Singapore Med J
, vol.21
, pp. 556
-
-
Boon, W.H.1
-
108
-
-
0023055059
-
Glucose-6-phosphate dehydrogenase deficiency: A preventable cause of mental retardation
-
Fok T, Lau S: Glucose-6-phosphate dehydrogenase deficiency: A preventable cause of mental retardation. BMJ 292:829, 1986
-
(1986)
BMJ
, vol.292
, pp. 829
-
-
Fok, T.1
Lau, S.2
-
109
-
-
0015835607
-
Salicylamidc glucuronide formation in newborns with severe jaundice of unknown etiology and due to glucose 6 phosphate dehydrogenase deficiency in Greece
-
Malaka-Zafiriu K, Tsiures I, Danielides B, Cassimos C: Salicylamidc glucuronide formation in newborns with severe jaundice of unknown etiology and due to glucose 6 phosphate dehydrogenase deficiency in Greece. Helv Paediatr Acta 28:323, 1973
-
(1973)
Helv Paediatr Acta
, vol.28
, pp. 323
-
-
Malaka-Zafiriu, K.1
Tsiures, I.2
Danielides, B.3
Cassimos, C.4
-
110
-
-
0015714191
-
Neonatal hyperbilirubinemia and glucose-6-phosphate dehydrogenase deficiency
-
Milbauer B, Peled N, Svirsky S: Neonatal hyperbilirubinemia and glucose-6-phosphate dehydrogenase deficiency. Isr J Med Sci 9:1547, 1973
-
(1973)
Isr J Med Sci
, vol.9
, pp. 1547
-
-
Milbauer, B.1
Peled, N.2
Svirsky, S.3
-
111
-
-
0026697796
-
Neonatal hyperbilirubinemia associated with glucose-6-phosphate dehydrogenase deficiency in Sephardic-Jewish neonates: Incidence, severity, and the effect of phototherapy
-
Kaplan M, Abramov A: Neonatal hyperbilirubinemia associated with glucose-6-phosphate dehydrogenase deficiency in Sephardic-Jewish neonates: Incidence, severity, and the effect of phototherapy. Pediatrics 90:401, 1992
-
(1992)
Pediatrics
, vol.90
, pp. 401
-
-
Kaplan, M.1
Abramov, A.2
-
112
-
-
0006896358
-
Serum bilirubin levels and glucose-6-phosphate dehydrogenase deficiency in newborn American negroes
-
O'Flynn MED, Hsia DY: Serum bilirubin levels and glucose-6-phosphate dehydrogenase deficiency in newborn American negroes. J Pediatr 63:160, 1963
-
(1963)
J Pediatr
, vol.63
, pp. 160
-
-
O'Flynn, M.E.D.1
Hsia, D.Y.2
-
113
-
-
0006988726
-
Peripheral blood and bilirubin values in normal full-term primaquine-sensitive negro infants: Effect of vitamin K
-
13. Zinkham WH: Peripheral blood and bilirubin values in normal full-term primaquine-sensitive negro infants: Effect of vitamin K. Pediatrics 31:983, 1963
-
(1963)
Pediatrics
, vol.31
, pp. 983
-
-
Zinkham, W.H.1
-
114
-
-
0017162540
-
The significance of glucose-6-phosphate dehy-drogenase deficiency in pregnancy
-
Perkins RP: The significance of glucose-6-phosphate dehy-drogenase deficiency in pregnancy. Am J Obstet Gynecol 125:215, 1976
-
(1976)
Am J Obstet Gynecol
, vol.125
, pp. 215
-
-
Perkins, R.P.1
-
115
-
-
0015096703
-
Glucose-6-phosphate dehydrogenase deficiency and hyperbilirubinemia in the newborn
-
Lopez R, Cooperman JM: Glucose-6-phosphate dehydrogenase deficiency and hyperbilirubinemia in the newborn. Am J Dis Child 122:66, 1971
-
(1971)
Am J Dis Child
, vol.122
, pp. 66
-
-
Lopez, R.1
Cooperman, J.M.2
-
116
-
-
0024852754
-
Relationship between exposure to icterogenic agents, glucose-6-phosphate dehydrogenase deficiency and neonatal jaundice in Nigeria
-
Owa JA: Relationship between exposure to icterogenic agents, glucose-6-phosphate dehydrogenase deficiency and neonatal jaundice in Nigeria. Acta Paediatr Scand 78:848, 1989
-
(1989)
Acta Paediatr Scand
, vol.78
, pp. 848
-
-
Owa, J.A.1
-
117
-
-
0017167610
-
Erythrocyte glucose 6-phosphate dehydrogenase deficiency (G6PD type A-) and neonatal jaundice
-
Bienzle U, Effiong C, Luzzatto L: Erythrocyte glucose 6-phosphate dehydrogenase deficiency (G6PD type A-) and neonatal jaundice. Acta Paediatr Scand 65:701, 1976
-
(1976)
Acta Paediatr Scand
, vol.65
, pp. 701
-
-
Bienzle, U.1
Effiong, C.2
Luzzatto, L.3
-
118
-
-
1142266185
-
Glucose-6-phosphate dehydrogenase deficiency and neonatal jaundice in Nigeria. Their relation to use of prophylactic vitamin K
-
Capps FPA, Gilles HM, Jolly H, Worlledge SM: Glucose-6-phosphate dehydrogenase deficiency and neonatal jaundice in Nigeria. Their relation to use of prophylactic vitamin K. Lancet 2:379, 1963
-
(1963)
Lancet
, vol.2
, pp. 379
-
-
Capps, F.P.A.1
Gilles, H.M.2
Jolly, H.3
Worlledge, S.M.4
-
119
-
-
0014800710
-
The poststorage viability of glucose-6-phosphate dehydrogenase-deficient erythrocytes
-
Orlina AR, Josephson AM, McDonald BJ: The poststorage viability of glucose-6-phosphate dehydrogenase-deficient erythrocytes. J Lab Clin Med 75:930, 1970
-
(1970)
J Lab Clin Med
, vol.75
, pp. 930
-
-
Orlina, A.R.1
Josephson, A.M.2
McDonald, B.J.3
-
120
-
-
0016640905
-
Glucose-6-phosphate dehydrogenase deficiency and blood transfusion
-
McCurdy PR, Morse EE: Glucose-6-phosphate dehydrogenase deficiency and blood transfusion. Vox Sang 28:230, 1975
-
(1975)
Vox Sang
, vol.28
, pp. 230
-
-
McCurdy, P.R.1
Morse, E.E.2
-
121
-
-
78651157030
-
Glucose-6-phosphate dehydrogenase deficiency in red cells. Incidence in the Curacao population, its clinical and genetic aspects
-
Van der Sar A, Schouten H, Struyker Boudier AM: Glucose-6-phosphate dehydrogenase deficiency in red cells. Incidence in the Curacao population, its clinical and genetic aspects. Enzyme 27:289, 1964
-
(1964)
Enzyme
, vol.27
, pp. 289
-
-
Van Der Sar, A.1
Schouten, H.2
Struyker Boudier, A.M.3
-
122
-
-
0027394935
-
Posttransfusional hemolysis in recipients of glucose-6-phosphate dehydrogenase-deficient erythrocytes
-
Shalev O, Manny N, Sharon R: Posttransfusional hemolysis in recipients of glucose-6-phosphate dehydrogenase-deficient erythrocytes. Vox Sang 64:94, 1993
-
(1993)
Vox Sang
, vol.64
, pp. 94
-
-
Shalev, O.1
Manny, N.2
Sharon, R.3
-
123
-
-
15844430740
-
Glucose-6-phosphate dehydrogenase deficiency in blood donors
-
Knox-Macaulay HHM: Glucose-6-phosphate dehydrogenase deficiency in blood donors. Saudi Med J 8:325, 1987
-
(1987)
Saudi Med J
, vol.8
, pp. 325
-
-
Knox-Macaulay, H.H.M.1
-
124
-
-
0028115855
-
Acute intravascular haemolysis following exchange transfusion with G-6-PD deficient blood
-
Kumar P, Sarkar S, Narang A: Acute intravascular haemolysis following exchange transfusion with G-6-PD deficient blood. Eur J Pediatr 153:98, 1994
-
(1994)
Eur J Pediatr
, vol.153
, pp. 98
-
-
Kumar, P.1
Sarkar, S.2
Narang, A.3
-
125
-
-
0024658551
-
Exchange transfusion with G-6-PD deficient donor blood causes exaggeration of neonatal hyperbilirubinemia
-
Gulati S, Singh S, Narang A, Bhakoo ON: Exchange transfusion with G-6-PD deficient donor blood causes exaggeration of neonatal hyperbilirubinemia. Indian Pediatr 26:499, 1989
-
(1989)
Indian Pediatr
, vol.26
, pp. 499
-
-
Gulati, S.1
Singh, S.2
Narang, A.3
Bhakoo, O.N.4
-
126
-
-
0022613120
-
G6PD-deficiency donor blood as a cause of hemolysis in two preterm infants
-
Mimouni F, Shohat S, Reisner SH: G6PD-deficiency donor blood as a cause of hemolysis in two preterm infants. Isr J Med Sci 22:120, 1986
-
(1986)
Isr J Med Sci
, vol.22
, pp. 120
-
-
Mimouni, F.1
Shohat, S.2
Reisner, S.H.3
-
127
-
-
36949073143
-
Gene action in erythrocyte deficiency of glucose-6-phosphate dehydrogenase: Tissue enzyme-levels
-
Marks PA, Gross RT, Hurwitz RE: Gene action in erythrocyte deficiency of glucose-6-phosphate dehydrogenase: Tissue enzyme-levels. Nature 183:1266, 1959
-
(1959)
Nature
, vol.183
, pp. 1266
-
-
Marks, P.A.1
Gross, R.T.2
Hurwitz, R.E.3
-
128
-
-
73049138765
-
Glucose-6-phosphate dehydrogenase activity in platelets
-
Wurzel H, McCreary T, Baker L, Gumerman L: Glucose-6-phosphate dehydrogenase activity in platelets. Blood 17:314, 1961
-
(1961)
Blood
, vol.17
, pp. 314
-
-
Wurzel, H.1
McCreary, T.2
Baker, L.3
Gumerman, L.4
-
129
-
-
0000163429
-
A study of subjects with erythrocyte glucose-6-phosphate dehydrogenase deficiency. II. Investigation of leukocyte enzymes
-
Ramot B, Fisher S, Szeinberg A, Adam A, Sheba C, Ganni D: A study of subjects with erythrocyte glucose-6-phosphate dehydrogenase deficiency. II. Investigation of leukocyte enzymes. J Clin Invest 38:2234, 1959
-
(1959)
J Clin Invest
, vol.38
, pp. 2234
-
-
Ramot, B.1
Fisher, S.2
Szeinberg, A.3
Adam, A.4
Sheba, C.5
Ganni, D.6
-
130
-
-
0019129768
-
Leucocyte glucose-6-phosphate dehydrogenase (G-6-PD) activity in G-6-PD deficient subjects
-
Tzortzatou-Stathopolou F, Zannos-Mariolea L, Karayiannis P, Constantsas N, Matsaniotis N: Leucocyte glucose-6-phosphate dehydrogenase (G-6-PD) activity in G-6-PD deficient subjects. Eur J Pediatr 135:37, 1980
-
(1980)
Eur J Pediatr
, vol.135
, pp. 37
-
-
Tzortzatou-Stathopolou, F.1
Zannos-Mariolea, L.2
Karayiannis, P.3
Constantsas, N.4
Matsaniotis, N.5
-
131
-
-
9544252766
-
Erythrocyte glucose-6-phosphate dehydrogenase deficient subjects: Enzyme-level in saliva
-
Ramot B, Sheba C, Adam A, Ashkenasi I: Erythrocyte glucose-6-phosphate dehydrogenase deficient subjects: Enzyme-level in saliva. Nature 185:931, 1960
-
(1960)
Nature
, vol.185
, pp. 931
-
-
Ramot, B.1
Sheba, C.2
Adam, A.3
Ashkenasi, I.4
-
132
-
-
84936429180
-
Nuove acquisizioni in tema di bio-enzimologia del favismo ittero-emoglobinurico. Nota III. L'attivit̀a Oglucosio-6-fosfato deidrogenasica del parenchima epatico
-
Brunetti P, Rossetti R, Broccia G: Nuove acquisizioni in tema di bio-enzimologia del favismo ittero-emoglobinurico. Nota III. L'attivit̀a Oglucosio-6-fosfato deidrogenasica del parenchima epatico. Clin Ther 32:338, 1960
-
(1960)
Clin Ther
, vol.32
, pp. 338
-
-
Brunetti, P.1
Rossetti, R.2
Broccia, G.3
-
133
-
-
0018640530
-
Genetically determined deficiency of glucose 6-phosphate dehydrogenase (type A-) is expressed in the liver
-
Oluboyede OA, Esan GJF, Francis TI, Luzzatto L: Genetically determined deficiency of glucose 6-phosphate dehydrogenase (type A-) is expressed in the liver. J Lab Clin Med 93:783, 1979
-
(1979)
J Lab Clin Med
, vol.93
, pp. 783
-
-
Oluboyede, O.A.1
Esan, G.J.F.2
Francis, T.I.3
Luzzatto, L.4
-
135
-
-
9544237718
-
Glucose-6-phosphate dehydrogenase deficient mutant in human cell culture
-
Gartler SM, Gandini E, Ceppellini R: Glucose-6-phosphate dehydrogenase deficient mutant in human cell culture. Nature 193:602, 1962
-
(1962)
Nature
, vol.193
, pp. 602
-
-
Gartler, S.M.1
Gandini, E.2
Ceppellini, R.3
-
136
-
-
0013823367
-
Tissue enzyme levels in erythrocyte glucose-6-phosphate dehydrogenase deficiency
-
Chan TK, Todd D, Wong CC: Tissue enzyme levels in erythrocyte glucose-6-phosphate dehydrogenase deficiency. J Lab Clin Med 66:937, 1965
-
(1965)
J Lab Clin Med
, vol.66
, pp. 937
-
-
Chan, T.K.1
Todd, D.2
Wong, C.C.3
-
137
-
-
0345562839
-
Enzyme studies on lenses from persons with primaquine-sensitive erythrocytes
-
Zinkham WH: Enzyme studies on lenses from persons with primaquine-sensitive erythrocytes. Am J Dis Child 100:525, 1960
-
(1960)
Am J Dis Child
, vol.100
, pp. 525
-
-
Zinkham, W.H.1
-
138
-
-
0017188682
-
Glucose-6-phosphate dehydrogenase in cataracts of subjects suffering from favism
-
Orzalesi N, Sorcinelli R, Binaghi F: Glucose-6-phosphate dehydrogenase in cataracts of subjects suffering from favism. Ophthalmic Res 8:192, 1976
-
(1976)
Ophthalmic Res
, vol.8
, pp. 192
-
-
Orzalesi, N.1
Sorcinelli, R.2
Binaghi, F.3
-
139
-
-
10144244170
-
The hemolytic effect of primaquine. I. The localization of the drug-induced hemolytic detect in primaquine-sensitive individuals
-
Dern RJ, Weinstein IM, Le Roy GV, Talmage DW, Alving AS: The hemolytic effect of primaquine. I. The localization of the drug-induced hemolytic detect in primaquine-sensitive individuals. J Lab Clin Med 43:303, 1954
-
(1954)
J Lab Clin Med
, vol.43
, pp. 303
-
-
Dern, R.J.1
Weinstein, I.M.2
Le Roy, G.V.3
Talmage, D.W.4
Alving, A.S.5
-
140
-
-
0345218201
-
The hemolytic effect of primaquine. XII. Shortened erythrocyte life span in primaquine-sensitive male negroes in the absence of drug administration
-
Brewer GJ, Tarlov AR, Kellermeyer RW: The hemolytic effect of primaquine. XII. Shortened erythrocyte life span in primaquine-sensitive male negroes in the absence of drug administration. J Lab Clin Med 58:217, 1961
-
(1961)
J Lab Clin Med
, vol.58
, pp. 217
-
-
Brewer, G.J.1
Tarlov, A.R.2
Kellermeyer, R.W.3
-
141
-
-
0018956451
-
Reduced chronic hemolysts during high-dose vitamin E administration in Mediterranean-type glucose-6-phosphate dehydrogenase deficiency
-
Corash L, Spielberg S, Bartsocas C, Boxer L, Steinherz R, Sheetz M, Egan M, Schlessleman J, Schulmun JD: Reduced chronic hemolysts during high-dose vitamin E administration in Mediterranean-type glucose-6-phosphate dehydrogenase deficiency. N Engl J Med 303:416, 1980
-
(1980)
N Engl J Med
, vol.303
, pp. 416
-
-
Corash, L.1
Spielberg, S.2
Bartsocas, C.3
Boxer, L.4
Steinherz, R.5
Sheetz, M.6
Egan, M.7
Schlessleman, J.8
Schulmun, J.D.9
-
142
-
-
0014591474
-
Hemolytic effects of standard single dosages of primaquine and chloroquine on G-6-PD-deficient Caucasians
-
Pannacciulli I, Salvidio E, Tizianello A, Parravidino G: Hemolytic effects of standard single dosages of primaquine and chloroquine on G-6-PD-deficient Caucasians. J Lab Clin Med 74:653, 1969
-
(1969)
J Lab Clin Med
, vol.74
, pp. 653
-
-
Pannacciulli, I.1
Salvidio, E.2
Tizianello, A.3
Parravidino, G.4
-
143
-
-
0345437424
-
Survival of 51 Cr-labelled red cells in subjects with thalassemia-trait or G6PD deficiency or both abnormalities
-
Bernini L, Latte B, Siniscalco M, Piomelli S, Spada U, Adinolfi M, Mollison PL: Survival of 51 Cr-labelled red cells in subjects with thalassemia-trait or G6PD deficiency or both abnormalities. Br J Haematol 10:171, 1964
-
(1964)
Br J Haematol
, vol.10
, pp. 171
-
-
Bernini, L.1
Latte, B.2
Siniscalco, M.3
Piomelli, S.4
Spada, U.5
Adinolfi, M.6
Mollison, P.L.7
-
144
-
-
0018865522
-
Interaction between the glucose-6-phosphate dehydrogenase deficiency and thalassaemia genes at phenotype level
-
Sanna G, Frau F, Melis MA, Galanello R, De Virgiliis S, Cao A: Interaction between the glucose-6-phosphate dehydrogenase deficiency and thalassaemia genes at phenotype level. Br J Haematol 44:555, 1980
-
(1980)
Br J Haematol
, vol.44
, pp. 555
-
-
Sanna, G.1
Frau, F.2
Melis, M.A.3
Galanello, R.4
De Virgiliis, S.5
Cao, A.6
-
145
-
-
0027449353
-
Low-grade haemolysis and assessment of iron status during the steady state in G6PD-deficient subjects
-
Ragusa R, Di Cataldo A, Gangarossa S, Lo Nigro L, Schilir̀o G: Low-grade haemolysis and assessment of iron status during the steady state in G6PD-deficient subjects. Acta Haematol 90:25, 1993
-
(1993)
Acta Haematol
, vol.90
, pp. 25
-
-
Ragusa, R.1
Di Cataldo, A.2
Gangarossa, S.3
Lo Nigro, L.4
Schilir̀o, G.5
-
146
-
-
0014528159
-
The haematological effects of glucose-6-phosphate dehydrogenase deficiency and thalassaemia trait: Interaction between the two genes at the phenotype level
-
Piomelli S, Siniscalco M: The haematological effects of glucose-6-phosphate dehydrogenase deficiency and thalassaemia trait: Interaction between the two genes at the phenotype level. Br J Haematol 16:537, 1969
-
(1969)
Br J Haematol
, vol.16
, pp. 537
-
-
Piomelli, S.1
Siniscalco, M.2
-
147
-
-
0014929946
-
Prevalence of sickle-cell trait and glucose-6-phosphate dehydrogenase deficiency
-
Petrakis NL, Wiesenfeld SL, Sams BJ, Collen MF. Cutler JL, Siegelaub AB: Prevalence of sickle-cell trait and glucose-6-phosphate dehydrogenase deficiency. N Engl J Med 282:767, 1970
-
(1970)
N Engl J Med
, vol.282
, pp. 767
-
-
Petrakis, N.L.1
Wiesenfeld, S.L.2
Sams, B.J.3
Collen, M.F.4
Cutler, J.L.5
Siegelaub, A.B.6
-
148
-
-
0018759047
-
Clinical implications of sickle-cell trait and glucose-6-phosphate dehydrogenase deficiency in hospitalized black male patients
-
Heller P, Best WR, Nelson RB, Becktel J: Clinical implications of sickle-cell trait and glucose-6-phosphate dehydrogenase deficiency in hospitalized black male patients. N Engl J Med 300:1001, 1979
-
(1979)
N Engl J Med
, vol.300
, pp. 1001
-
-
Heller, P.1
Best, W.R.2
Nelson, R.B.3
Becktel, J.4
-
149
-
-
0344344573
-
Glucose-6-phos-phate dehydrogenase deficiency and the incidence of cancer
-
Beaconsfield P, Rainsbury R, Kalton G: Glucose-6-phos-phate dehydrogenase deficiency and the incidence of cancer. Oncology 19:11, 1965
-
(1965)
Oncology
, vol.19
, pp. 11
-
-
Beaconsfield, P.1
Rainsbury, R.2
Kalton, G.3
-
150
-
-
0014417777
-
Osservazioni preliminari sull'incidenza neoplastica e sul comportamento enzimatico e proliferativo del tessuto tumorale negli individui carenti di glucosio-6-fosfato deidrogenasi (G-6-PD)
-
Sulis E, Spano G: Osservazioni preliminari sull'incidenza neoplastica e sul comportamento enzimatico e proliferativo del tessuto tumorale negli individui carenti di glucosio-6-fosfato deidrogenasi (G-6-PD). Boll Soc Ital Biol Sper 44:1246, 1968
-
(1968)
Boll Soc Ital Biol Sper
, vol.44
, pp. 1246
-
-
Sulis, E.1
Spano, G.2
-
151
-
-
0015176179
-
The association between glucose6-phosphate dehydrogenase deficiency and cancer in American negroes
-
Naik SN, Anderson DE: The association between glucose6-phosphate dehydrogenase deficiency and cancer in American negroes. Oncology 25:356, 1971
-
(1971)
Oncology
, vol.25
, pp. 356
-
-
Naik, S.N.1
Anderson, D.E.2
-
152
-
-
0015525856
-
G-6-PD deficiency and cancer
-
Sulis E: G-6-PD deficiency and cancer. Lancet 1:1185, 1972
-
(1972)
Lancet
, vol.1
, pp. 1185
-
-
Sulis, E.1
-
154
-
-
0024591714
-
Glucose-6-phosphate dehydrogenase deficiency and cancer in a Sardinian male population: A case-control study
-
Cocco P, Dessi S, Avataneo G, Picchiri G, Heinemann E: Glucose-6-phosphate dehydrogenase deficiency and cancer in a Sardinian male population: A case-control study. Carcinogenesis 10:813, 1989
-
(1989)
Carcinogenesis
, vol.10
, pp. 813
-
-
Cocco, P.1
Dessi, S.2
Avataneo, G.3
Picchiri, G.4
Heinemann, E.5
-
155
-
-
0024244473
-
G6PD deficiency and breast cancer
-
Forteleoni G, Argiolas L, Farris A, Ferraris AM, Gaetani GF, Meloni T: G6PD deficiency and breast cancer. Tumori 74:665, 1988
-
(1988)
Tumori
, vol.74
, pp. 665
-
-
Forteleoni, G.1
Argiolas, L.2
Farris, A.3
Ferraris, A.M.4
Gaetani, G.F.5
Meloni, T.6
-
156
-
-
0015527226
-
Human erythrocyte glucose 6-phosphate dehydrogenase: Electron microscope studies on structure and interconversion of tetramers, dimers and monomers
-
Wrigley NG, Heather JV, Bonsignore A, De Flora A: Human erythrocyte glucose 6-phosphate dehydrogenase: Electron microscope studies on structure and interconversion of tetramers, dimers and monomers. J Mol Biol 68:483, 1972
-
(1972)
J Mol Biol
, vol.68
, pp. 483
-
-
Wrigley, N.G.1
Heather, J.V.2
Bonsignore, A.3
De Flora, A.4
-
157
-
-
0014403419
-
Glucose-6-phosphate dehydrogenase from human erythrocytes: Molecular weight determination by gel filtration
-
Rattazzi MC: Glucose-6-phosphate dehydrogenase from human erythrocytes: Molecular weight determination by gel filtration. Biochem Biophys Res Commun 31:16, 1968
-
(1968)
Biochem Biophys Res Commun
, vol.31
, pp. 16
-
-
Rattazzi, M.C.1
-
158
-
-
0016211326
-
Human erythrocyte glucose 6-phosphate dehydrogenase. Content of bound coenzyme
-
De Flora A, Morelli A, Giuliano F: Human erythrocyte glucose 6-phosphate dehydrogenase. Content of bound coenzyme. Biochem Biophys Res Commun 59:406, 1974
-
(1974)
Biochem Biophys Res Commun
, vol.59
, pp. 406
-
-
De Flora, A.1
Morelli, A.2
Giuliano, F.3
-
159
-
-
0017180141
-
Human erythrocyte glucose-6-phosphate dehydrogenase. Evidence for competitive binding of NADP and NADPH
-
Morelli A, Benatti U, Guiliano F, De Flora A: Human erythrocyte glucose-6-phosphate dehydrogenase. Evidence for competitive binding of NADP and NADPH. Biochem Biophys Res Commun 70:600, 1976
-
(1976)
Biochem Biophys Res Commun
, vol.70
, pp. 600
-
-
Morelli, A.1
Benatti, U.2
Guiliano, F.3
De Flora, A.4
-
160
-
-
73849179051
-
Glucose-6-phosphate dehydrogenase from human erythrocytes. II. Subactive states of the enzyme from normal persons
-
Kirkman HN, Hendrickson EM: Glucose-6-phosphate dehydrogenase from human erythrocytes. II. Subactive states of the enzyme from normal persons. J Biol Chem 237:2371, 1962
-
(1962)
J Biol Chem
, vol.237
, pp. 2371
-
-
Kirkman, H.N.1
Hendrickson, E.M.2
-
161
-
-
0016170092
-
Human erythrocyte glucose 6-phosphate dehydrogenase. Interaction with oxidized and reduced coenzyme
-
De Flora A, Morelli A, Benatti U, Giuliano F, Molinari MP: Human erythrocyte glucose 6-phosphate dehydrogenase. Interaction with oxidized and reduced coenzyme. Biochem Biophys Res Commun 60:999, 1974
-
(1974)
Biochem Biophys Res Commun
, vol.60
, pp. 999
-
-
De Flora, A.1
Morelli, A.2
Benatti, U.3
Giuliano, F.4
Molinari, M.P.5
-
162
-
-
0025863168
-
Bound and unbound pyridine dinucleotides in normal and glucose-6-phosphate dehydrogenase-deficient erythrocytes
-
Canepa L, Ferraris AM, Miglino M, Gaetani GF: Bound and unbound pyridine dinucleotides in normal and glucose-6-phosphate dehydrogenase-deficient erythrocytes. Biochim Biophys Acta 1074:101, 1991
-
(1991)
Biochim Biophys Acta
, vol.1074
, pp. 101
-
-
Canepa, L.1
Ferraris, A.M.2
Miglino, M.3
Gaetani, G.F.4
-
164
-
-
0025765204
-
Functionally important regions of glucose-6-phosphate dehydrogenase defined by the Saccharomyces cerevisiae enzyme and its differences from the mammalian and insect forms
-
Persson B, J̈ornvall H, Wood I, Jeffery J: Functionally important regions of glucose-6-phosphate dehydrogenase defined by the Saccharomyces cerevisiae enzyme and its differences from the mammalian and insect forms. Eur J Biochem 198:485, 1991
-
(1991)
Eur J Biochem
, vol.198
, pp. 485
-
-
Persson, B.1
J̈ornvall, H.2
Wood, I.3
Jeffery, J.4
-
165
-
-
0023945415
-
Human erythrocyte glucose-6-phosphate dehydrogenase: Identification of a reactive lysyl residue labelled with pyridoxal 5′-phosphate
-
Camardella L, Caruso C, Rutigliano B, Romano M, Di Prisco G, Descalzi-Cancedda F: Human erythrocyte glucose-6-phosphate dehydrogenase: Identification of a reactive lysyl residue labelled with pyridoxal 5′-phosphate. Eur J Biochem 171:485, 1988
-
(1988)
Eur J Biochem
, vol.171
, pp. 485
-
-
Camardella, L.1
Caruso, C.2
Rutigliano, B.3
Romano, M.4
Di Prisco, G.5
Descalzi-Cancedda, F.6
-
166
-
-
0024970423
-
Glucose-6-phosphale dehydrogenase. Characterization of a reactive lysine residue in the Pichia jadinii enzyme reveals a limited structural variation in a functionally significant segment
-
Jeffery J, Wood I, Macleod A, Jeffery R, Jornvall H: Glucose-6-phosphale dehydrogenase. Characterization of a reactive lysine residue in the Pichia jadinii enzyme reveals a limited structural variation in a functionally significant segment. Biochem Biophys Res Commun 160:1290, 1989
-
(1989)
Biochem Biophys Res Commun
, vol.160
, pp. 1290
-
-
Jeffery, J.1
Wood, I.2
Macleod, A.3
Jeffery, R.4
Jornvall, H.5
-
167
-
-
0021993045
-
Glucose-6-phosphate dehydrogenase from Saccharomyces cerevisiae: Characterization of a reactive lysine residue labeled with acetylsalicylic acid
-
Jeffery J, Hobbs L, Jornvall H: Glucose-6-phosphate dehydrogenase from Saccharomyces cerevisiae: Characterization of a reactive lysine residue labeled with acetylsalicylic acid. Biochemistry 24:666, 1985
-
(1985)
Biochemistry
, vol.24
, pp. 666
-
-
Jeffery, J.1
Hobbs, L.2
Jornvall, H.3
-
168
-
-
0023090394
-
Sequence identity between a lysine-containing peptide from Leuconostoc mesenteroides glucose-6-phosphate dehydrogenase and an active site peptide from human erythrocyte glucose-6-phosphate dehydrogenase
-
Bhadbhade MM, Adams MJ, Flynn TG, Levy HR: Sequence identity between a lysine-containing peptide from Leuconostoc mesenteroides glucose-6-phosphate dehydrogenase and an active site peptide from human erythrocyte glucose-6-phosphate dehydrogenase. FEBS Lett 211:243, 1987
-
(1987)
FEBS Lett
, vol.211
, pp. 243
-
-
Bhadbhade, M.M.1
Adams, M.J.2
Flynn, T.G.3
Levy, H.R.4
-
169
-
-
0024595407
-
Catalase and glutathione peroxidase are equally active in detoxification of hydrogen peroxide in human erythrocytes
-
Gaetani GF, Galiano S, Canepa L, Ferraris AM, Kirkman HN: Catalase and glutathione peroxidase are equally active in detoxification of hydrogen peroxide in human erythrocytes. Blood 73:334, 1989
-
(1989)
Blood
, vol.73
, pp. 334
-
-
Gaetani, G.F.1
Galiano, S.2
Canepa, L.3
Ferraris, A.M.4
Kirkman, H.N.5
-
170
-
-
0014842393
-
Glutathione metabolism of the erythrocyte. The enzymic cleavage of glutathione-haemoglobin preparations by glutathione reductase
-
Srivastava SK, Beutler E: Glutathione metabolism of the erythrocyte. The enzymic cleavage of glutathione-haemoglobin preparations by glutathione reductase. Biochem J 119:353, 1970
-
(1970)
Biochem J
, vol.119
, pp. 353
-
-
Srivastava, S.K.1
Beutler, E.2
-
171
-
-
0009424743
-
Catalase: A tetrameric enzyme with four tightly bound molecules of NADPH
-
Kirkman HN, Gaetani GF: Catalase: A tetrameric enzyme with four tightly bound molecules of NADPH. Proc Natl Acad Sci USA 81:4343, 1984
-
(1984)
Proc Natl Acad Sci USA
, vol.81
, pp. 4343
-
-
Kirkman, H.N.1
Gaetani, G.F.2
-
173
-
-
0023931683
-
Recent developments on Mediterranean G6PD
-
Gaetani GF. Ferraris AM: Recent developments on Mediterranean G6PD. Br J Haematol 68:1, 1988
-
(1988)
Br J Haematol
, vol.68
, pp. 1
-
-
Gaetani, G.F.1
Ferraris, A.M.2
-
174
-
-
0019984658
-
Erythrocyte Superoxide dismutase, catalase and glutathione peroxidase in glucose-6-phosphate dehydrogenase deficiency
-
Gerli GC, Beretta L, Bianchi M, Agostoni A, Gualandri V, Orsini GB: Erythrocyte Superoxide dismutase, catalase and glutathione peroxidase in glucose-6-phosphate dehydrogenase deficiency. Scand J Haematol 29:135, 1982
-
(1982)
Scand J Haematol
, vol.29
, pp. 135
-
-
Gerli, G.C.1
Beretta, L.2
Bianchi, M.3
Agostoni, A.4
Gualandri, V.5
Orsini, G.B.6
-
175
-
-
0025827312
-
Erythrocyte defense against hydrogen peroxide: Preeminent importance of catalase
-
Scott MD, Lubin BH, Zuo L, Kuypers FA: Erythrocyte defense against hydrogen peroxide: Preeminent importance of catalase. J Lab Clin Med 118:7, 1991
-
(1991)
J Lab Clin Med
, vol.118
, pp. 7
-
-
Scott, M.D.1
Lubin, B.H.2
Zuo, L.3
Kuypers, F.A.4
-
176
-
-
33947476438
-
Glutathione peroxidase: The primary agent for the elimination of hydrogen peroxide in erythrocytes
-
Cohen G, Hochstein P: Glutathione peroxidase: The primary agent for the elimination of hydrogen peroxide in erythrocytes. Biochemistry 2:1420, 1963
-
(1963)
Biochemistry
, vol.2
, pp. 1420
-
-
Cohen, G.1
Hochstein, P.2
-
178
-
-
0022976939
-
Regulation of glucose-6-phosphate dehydrogenase in human erythrocytes
-
Kirkman HN, Gaetani GF: Regulation of glucose-6-phosphate dehydrogenase in human erythrocytes. J Biol Chem 261:4032, 1986
-
(1986)
J Biol Chem
, vol.261
, pp. 4032
-
-
Kirkman, H.N.1
Gaetani, G.F.2
-
179
-
-
77049306406
-
The glutathione instability of drug-sensitive red cells. A new method for the in vitro detection of drug-sensitivity
-
Beutler E: The glutathione instability of drug-sensitive red cells. A new method for the in vitro detection of drug-sensitivity. J Lab Clin Med 49:84, 1957
-
(1957)
J Lab Clin Med
, vol.49
, pp. 84
-
-
Beutler, E.1
-
180
-
-
9544230466
-
A genetic study of a defect in glutathione metabolism of the erythrocyte
-
Childs B, Zinkham W, Browne EA, Kimbro EL, Torbert JV: A genetic study of a defect in glutathione metabolism of the erythrocyte. Johns Hopkins Med J 102:21, 1958
-
(1958)
Johns Hopkins Med J
, vol.102
, pp. 21
-
-
Childs, B.1
Zinkham, W.2
Browne, E.A.3
Kimbro, E.L.4
Torbert, J.V.5
-
181
-
-
0001434842
-
Glucose 6-phosphate dehydrogenase deficiency in red blood cells of East Africans
-
Allison AC: Glucose 6-phosphate dehydrogenase deficiency in red blood cells of East Africans. Nature 186:531, 1960
-
(1960)
Nature
, vol.186
, pp. 531
-
-
Allison, A.C.1
-
182
-
-
0012020558
-
Electrophoretic heterogeneity of glucose-6-phosphate dehydrogenase and its relationship to enzyme deficiency in man
-
Boyer SH, Porter IH, Weilbacher RG: Electrophoretic heterogeneity of glucose-6-phosphate dehydrogenase and its relationship to enzyme deficiency in man. Proc Natl Acad Sci USA 48:1868, 1962
-
(1962)
Proc Natl Acad Sci USA
, vol.48
, pp. 1868
-
-
Boyer, S.H.1
Porter, I.H.2
Weilbacher, R.G.3
-
183
-
-
0000780243
-
Linkage between deficiency of glucose-6-phosphate dehydrogenase and colour-blindness
-
Adam A: Linkage between deficiency of glucose-6-phosphate dehydrogenase and colour-blindness. Nature 189:686, 1961
-
(1961)
Nature
, vol.189
, pp. 686
-
-
Adam, A.1
-
184
-
-
50549157626
-
Chromosomal constitution in glucose-6-phosphate-dehydrogenase deficiency
-
Trujillo J, Fairbanks VF, Ohno S, Beutler E: Chromosomal constitution in glucose-6-phosphate-dehydrogenase deficiency. Lancet 2:1454, 1961
-
(1961)
Lancet
, vol.2
, pp. 1454
-
-
Trujillo, J.1
Fairbanks, V.F.2
Ohno, S.3
Beutler, E.4
-
185
-
-
0002826398
-
The normal human female as a mosaic of X-chromosome activity: Studies using the gene for G-6-PD deficiency as a marker
-
Beutler E, Yeh M, Fairbanks VF: The normal human female as a mosaic of X-chromosome activity: Studies using the gene for G-6-PD deficiency as a marker. Proc Natl Acad Sci USA 48:9, 1962
-
(1962)
Proc Natl Acad Sci USA
, vol.48
, pp. 9
-
-
Beutler, E.1
Yeh, M.2
Fairbanks, V.F.3
-
186
-
-
84932013613
-
Biochemical abnormalities associated with hemolytic states
-
Weinstein IM, Beutler E (eds): New York, NY, McGraw-Hill
-
Beutler E: Biochemical abnormalities associated with hemolytic states, in Weinstein IM, Beutler E (eds): Mechanisms of Anemia in Man, New York, NY, McGraw-Hill, 1962, p 195
-
(1962)
Mechanisms of Anemia in Man
, pp. 195
-
-
Beutler, E.1
-
187
-
-
7144223296
-
Gene action in the X-chromosome of the mouse (mus musculus l.)
-
Lyon MF: Gene action in the X-chromosome of the mouse (mus musculus l.). Nature 190:372, 1961
-
(1961)
Nature
, vol.190
, pp. 372
-
-
Lyon, M.F.1
-
188
-
-
0023503196
-
Multipoint genetic mapping of the Xq26-q28 region in families with fragile X mental retardation and in normal families reveals tight linkage of markers in q26-q27
-
Oberle I, Cumerino G, Wrogemann K, Arveiler B, Hanauer A, Raimondi E, Mandel JL: Multipoint genetic mapping of the Xq26-q28 region in families with fragile X mental retardation and in normal families reveals tight linkage of markers in q26-q27. Hum Genet 77:60, 1987
-
(1987)
Hum Genet
, vol.77
, pp. 60
-
-
Oberle, I.1
Cumerino, G.2
Wrogemann, K.3
Arveiler, B.4
Hanauer, A.5
Raimondi, E.6
Mandel, J.L.7
-
189
-
-
9544221394
-
Linkage between the X chromosome loci for glucose-6-phosphate dehydrogenase electrophoretic variation and hemophilia A
-
Boyer SH, Graham JB: Linkage between the X chromosome loci for glucose-6-phosphate dehydrogenase electrophoretic variation and hemophilia A. Am J Hum Genet 17:320, 1965
-
(1965)
Am J Hum Genet
, vol.17
, pp. 320
-
-
Boyer, S.H.1
Graham, J.B.2
-
190
-
-
0023881937
-
Normal and abnormal color-vision genes
-
Motulsky AG: Normal and abnormal color-vision genes. Am J Hum Genet 42:405, 1988
-
(1988)
Am J Hum Genet
, vol.42
, pp. 405
-
-
Motulsky, A.G.1
-
191
-
-
0027178843
-
G6PD haplotypes spanning Xq28 from F8C to red/green color vision
-
Filosa S, Calabro V, Lania G, Vulliamy TJ, Brancati C, Tagarelli A, Luzzatto L, Martini G: G6PD haplotypes spanning Xq28 from F8C to red/green color vision. Genomics 17:6, 1993
-
(1993)
Genomics
, vol.17
, pp. 6
-
-
Filosa, S.1
Calabro, V.2
Lania, G.3
Vulliamy, T.J.4
Brancati, C.5
Tagarelli, A.6
Luzzatto, L.7
Martini, G.8
-
192
-
-
0023146964
-
Genetic linkage between X-chromosome markers and bipolar affective illness
-
Baron M, Risch N, Hamburger R, Mandel B, Kushner S, Newman M, Drumer D, Belmaker RH: Genetic linkage between X-chromosome markers and bipolar affective illness. Nature 326:289, 1987
-
(1987)
Nature
, vol.326
, pp. 289
-
-
Baron, M.1
Risch, N.2
Hamburger, R.3
Mandel, B.4
Kushner, S.5
Newman, M.6
Drumer, D.7
Belmaker, R.H.8
-
193
-
-
0027179369
-
Actin-binding protein (ABP-280) filamin gene (FLN) maps telomeric to the color vision locus (R/GCP) and centromeric to G6PD in Xq28
-
Gorlin JB, Henske E, Warren ST, Kunst CB, D'Urso M, Palmieri G, Hartwig JH, Bruns G, Kwiatkowski DJ: Actin-binding protein (ABP-280) filamin gene (FLN) maps telomeric to the color vision locus (R/GCP) and centromeric to G6PD in Xq28. Genomics 17:496, 1993
-
(1993)
Genomics
, vol.17
, pp. 496
-
-
Gorlin, J.B.1
Henske, E.2
Warren, S.T.3
Kunst, C.B.4
D'Urso, M.5
Palmieri, G.6
Hartwig, J.H.7
Bruns, G.8
Kwiatkowski, D.J.9
-
194
-
-
0025095962
-
X-linked myopia: Bornholm eye disease. Linkage to DNA markers on the distal part of Xq
-
Schwanz M, Haim M, Skarsholm D: X-linked myopia: Bornholm eye disease. Linkage to DNA markers on the distal part of Xq. Clin Genet 38:281, 1990
-
(1990)
Clin Genet
, vol.38
, pp. 281
-
-
Schwanz, M.1
Haim, M.2
Skarsholm, D.3
-
195
-
-
0026624992
-
Clasped-thumb mental retardation (MASA) syndrome: Confirmation of linkage to Xq28
-
Macias VR, Day DW, King TE, Wilson GN: Clasped-thumb mental retardation (MASA) syndrome: confirmation of linkage to Xq28. Am J Med Genet 43:408, 1992
-
(1992)
Am J Med Genet
, vol.43
, pp. 408
-
-
Macias, V.R.1
Day, D.W.2
King, T.E.3
Wilson, G.N.4
-
196
-
-
0027216789
-
Dyskeratosis congenita: Three additional families show linkage to a locus in Xq28
-
Arngrimsson R, Dokal I, Luzzatto L, Connor JM: Dyskeratosis congenita: three additional families show linkage to a locus in Xq28. J Med Genet 30:618, 1993
-
(1993)
J Med Genet
, vol.30
, pp. 618
-
-
Arngrimsson, R.1
Dokal, I.2
Luzzatto, L.3
Connor, J.M.4
-
197
-
-
15844373424
-
Analysis of the primary structure of human G 6 PD deduced from the cDNA sequence
-
Yoshida A, Beutler E (eds): Orlando. FL, Academic
-
Persico MG, Viglietto G, Martini G, Dono R, D'Urso M, Toniolo D, Vulliamy T, Luzzatto L: Analysis of the primary structure of human G 6 PD deduced from the cDNA sequence, in Yoshida A, Beutler E (eds): Glucose-6-Phosphate Dehydrogenase, Orlando. FL, Academic, 1986, p 503
-
(1986)
Glucose-6-Phosphate Dehydrogenase
, pp. 503
-
-
Persico, M.G.1
Viglietto, G.2
Martini, G.3
Dono, R.4
D'Urso, M.5
Toniolo, D.6
Vulliamy, T.7
Luzzatto, L.8
-
198
-
-
0022762876
-
Structural analysis of the X-linked gene encoding human glucose 6-phosphate dehydrogenase
-
Martini G, Toniolo D, Vulliamy T, Luzzatto L, Dono R, Viglietto G, Paonessa G, D'Urso M, Persico MG: Structural analysis of the X-linked gene encoding human glucose 6-phosphate dehydrogenase. EMBO J 5:1849, 1986
-
(1986)
EMBO J
, vol.5
, pp. 1849
-
-
Martini, G.1
Toniolo, D.2
Vulliamy, T.3
Luzzatto, L.4
Dono, R.5
Viglietto, G.6
Paonessa, G.7
D'Urso, M.8
Persico, M.G.9
-
199
-
-
0021672173
-
Partial purification and characterization of the messenger RNA for human glucose-6-phosphate dehydrogenase
-
Toniolo D, Persico MG, Battistuzzi G, Luzzatto L: Partial purification and characterization of the messenger RNA for human glucose-6-phosphate dehydrogenase. Mol Biol Med 2:89, 1984
-
(1984)
Mol Biol Med
, vol.2
, pp. 89
-
-
Toniolo, D.1
Persico, M.G.2
Battistuzzi, G.3
Luzzatto, L.4
-
200
-
-
0025790419
-
Sequence of human glucose-6-phosphate dehydrogenase cloned in plasmids and a yeast artificial chromosome (YAC)
-
Chen EY, Cheng A, Lee A, Kuang W-J, Hillier L, Green P, Schlessinger D, Ciccodicola A, D'Urso M: Sequence of human glucose-6-phosphate dehydrogenase cloned in plasmids and a yeast artificial chromosome (YAC). Genomics 10:792, 1991
-
(1991)
Genomics
, vol.10
, pp. 792
-
-
Chen, E.Y.1
Cheng, A.2
Lee, A.3
Kuang, W.-J.4
Hillier, L.5
Green, P.6
Schlessinger, D.7
Ciccodicola, A.8
D'Urso, M.9
-
201
-
-
0023955912
-
Expression of the G6PD locus on the human X chromosome is associated with demethylation of three CpG islands within 100 kb of DNA
-
Toniolo D, Martini G, Migeon BR, Dono R: Expression of the G6PD locus on the human X chromosome is associated with demethylation of three CpG islands within 100 kb of DNA. EMBO J 7:401, 1988
-
(1988)
EMBO J
, vol.7
, pp. 401
-
-
Toniolo, D.1
Martini, G.2
Migeon, B.R.3
Dono, R.4
-
202
-
-
0025834624
-
The CpG island in the 5′ region of the G6PD gene of man and mouse
-
Toniolo D, Filippi M, Dono R, Lettieri T, Martini G: The CpG island in the 5′ region of the G6PD gene of man and mouse. Gene 102:197, 1991
-
(1991)
Gene
, vol.102
, pp. 197
-
-
Toniolo, D.1
Filippi, M.2
Dono, R.3
Lettieri, T.4
Martini, G.5
-
203
-
-
0025121480
-
High levels of transcription driven by a 400 bp segment of the human G6PD promoter
-
Ursini MV, Scalera L, Martini G: High levels of transcription driven by a 400 bp segment of the human G6PD promoter. Biochem Biophys Res Commun 170:1203, 1990
-
(1990)
Biochem Biophys Res Commun
, vol.170
, pp. 1203
-
-
Ursini, M.V.1
Scalera, L.2
Martini, G.3
-
204
-
-
0004497053
-
Molecular cloning and nucleotide sequence of cDNA for human glucose-6-phosphate dehydrogenase variant A(-)
-
Hirono A, Beutler E: Molecular cloning and nucleotide sequence of cDNA for human glucose-6-phosphate dehydrogenase variant A(-). Proc Natl Acad Sci USA 85:3951, 1988
-
(1988)
Proc Natl Acad Sci USA
, vol.85
, pp. 3951
-
-
Hirono, A.1
Beutler, E.2
-
205
-
-
0024558962
-
Alternative splicing of human glucose-6-phosphate dehydrogenase mRNA in different tissues
-
Hirono A, Beutler E: Alternative splicing of human glucose-6-phosphate dehydrogenase mRNA in different tissues. J Clin Invest 83:343, 1989
-
(1989)
J Clin Invest
, vol.83
, pp. 343
-
-
Hirono, A.1
Beutler, E.2
-
206
-
-
0027468902
-
Alternative splicing of human G6PD messenger RNA in K562 cells but not in cultured erythroblasts
-
Cappellini MD, Tavazzi D, Martinez di Montemuros F, Sampietro M, Gaviraghi A, Carandini D, Fiorelli G: Alternative splicing of human G6PD messenger RNA in K562 cells but not in cultured erythroblasts. Eur J Clin Invest 23:188, 1993
-
(1993)
Eur J Clin Invest
, vol.23
, pp. 188
-
-
Cappellini, M.D.1
Tavazzi, D.2
Martinez Di Montemuros, F.3
Sampietro, M.4
Gaviraghi, A.5
Carandini, D.6
Fiorelli, G.7
-
207
-
-
0024240178
-
The production of normal and variant human glucose6-phosphate dehydrogenase in cos cells
-
Mason PJ, Vulliamy TJ, Foulkes NS, Town M, Haidar B, Luzzatto L: The production of normal and variant human glucose6-phosphate dehydrogenase in cos cells. Eur J Biochem 178:109, 1988
-
(1988)
Eur J Biochem
, vol.178
, pp. 109
-
-
Mason, P.J.1
Vulliamy, T.J.2
Foulkes, N.S.3
Town, M.4
Haidar, B.5
Luzzatto, L.6
-
208
-
-
0024474055
-
Functional expression of human glucose-6-phosphate dehydrogenase in Escherichia coli
-
Persico MG, Ciccodicola A, Martini G, Rosner JL: Functional expression of human glucose-6-phosphate dehydrogenase in Escherichia coli. Gene 78:365, 1989
-
(1989)
Gene
, vol.78
, pp. 365
-
-
Persico, M.G.1
Ciccodicola, A.2
Martini, G.3
Rosner, J.L.4
-
209
-
-
0026551994
-
Purification and properties of human glucose-6-phosphate dehydrogenase made in E. coli
-
Bautista JM, Mason PJ, Luzzatto L: Purification and properties of human glucose-6-phosphate dehydrogenase made in E. coli. Biochim Biophys Acta 1119:74, 1992
-
(1992)
Biochim Biophys Acta
, vol.1119
, pp. 74
-
-
Bautista, J.M.1
Mason, P.J.2
Luzzatto, L.3
-
210
-
-
0028057464
-
Expression and biochemical characterization of human glucose-6-phosphate dehydrogenase in Escherichia coli: A system to analyze normal and mutant enzymes
-
Tang TK, Yeh C-H, Huang C-S, Huang M-J: Expression and biochemical characterization of human glucose-6-phosphate dehydrogenase in Escherichia coli: A system to analyze normal and mutant enzymes. Blood 83:1436, 1994
-
(1994)
Blood
, vol.83
, pp. 1436
-
-
Tang, T.K.1
Yeh, C.-H.2
Huang, C.-S.3
Huang, M.-J.4
-
211
-
-
0024323972
-
Two structural genes on different chromosomes are required for encoding a single chain human red cell glucose-6-phosphate dehydrogenase subunit
-
Kanno H, Huang I-Y, Kan YW, Yoshida A: Two structural genes on different chromosomes are required for encoding a single chain human red cell glucose-6-phosphate dehydrogenase subunit. Cell 58:595, 1989
-
(1989)
Cell
, vol.58
, pp. 595
-
-
Kanno, H.1
Huang, I.-Y.2
Kan, Y.W.3
Yoshida, A.4
-
212
-
-
0025367074
-
Human red cell glucose-6-phosphate dehydrogenase: All active enzyme has sequence predicted by the X-chromosome encoded cDNA
-
Beutler E, Gelbart T, Kuhl W: Human red cell glucose-6-phosphate dehydrogenase: All active enzyme has sequence predicted by the X-chromosome encoded cDNA. Cell 62:7, 1990
-
(1990)
Cell
, vol.62
, pp. 7
-
-
Beutler, E.1
Gelbart, T.2
Kuhl, W.3
-
213
-
-
0024976572
-
The human mRNA that provides the N-terminus of chimeric G6PD encodes GMP reductase
-
Henikoff S, Smith JM: The human mRNA that provides the N-terminus of chimeric G6PD encodes GMP reductase. Cell 58:1021, 1989
-
(1989)
Cell
, vol.58
, pp. 1021
-
-
Henikoff, S.1
Smith, J.M.2
-
214
-
-
0025310172
-
Origin of "fused" glucose-6-phosphate dehydrogenase
-
Yoshida A, Kan YW: Origin of "fused" glucose-6-phosphate dehydrogenase. Cell 62:11, 1990
-
(1990)
Cell
, vol.62
, pp. 11
-
-
Yoshida, A.1
Kan, Y.W.2
-
215
-
-
0025306945
-
Human red cell glucose-6-phosphate dehydrogenase is encoded only on the X chromosome
-
Mason PJ, Bautista JM, Vulliamy TJ, Turner N, Luzzatto L: Human red cell glucose-6-phosphate dehydrogenase is encoded only on the X chromosome. Cell 62:9, 1990
-
(1990)
Cell
, vol.62
, pp. 9
-
-
Mason, P.J.1
Bautista, J.M.2
Vulliamy, T.J.3
Turner, N.4
Luzzatto, L.5
-
216
-
-
0025763140
-
DNA sequence abnormalities of human glucose-6-phosphate dehydrogenase variants
-
Beutler E, Kuhl W, Gelbart T, Forman L: DNA sequence abnormalities of human glucose-6-phosphate dehydrogenase variants. J Biol Chem 266:4145, 1991
-
(1991)
J Biol Chem
, vol.266
, pp. 4145
-
-
Beutler, E.1
Kuhl, W.2
Gelbart, T.3
Forman, L.4
-
217
-
-
0025165882
-
Identification of a single base change in a new human mutant glucose-6-phosphate dehydrogenase gene by polymerase-chain-reaction amplification of the entire coding region from genomic DNA
-
Poggi V, Town M, Foulkes NS, Luzzatto L: Identification of a single base change in a new human mutant glucose-6-phosphate dehydrogenase gene by polymerase-chain-reaction amplification of the entire coding region from genomic DNA. Biochem J 271:157, 1990
-
(1990)
Biochem J
, vol.271
, pp. 157
-
-
Poggi, V.1
Town, M.2
Foulkes, N.S.3
Luzzatto, L.4
-
218
-
-
0026643947
-
Diverse point mutations result in glucose-6-phosphate dehydrogenase (G6PD) polymorphism in Taiwan
-
Tang TK, Huang C-S, Huang M-J, Tam K-B, Yeh C-H, Tang C-JC: Diverse point mutations result in glucose-6-phosphate dehydrogenase (G6PD) polymorphism in Taiwan. Blood 79:2135, 1992
-
(1992)
Blood
, vol.79
, pp. 2135
-
-
Tang, T.K.1
Huang, C.-S.2
Huang, M.-J.3
Tam, K.-B.4
Yeh, C.-H.5
Tang, C.-J.C.6
-
219
-
-
85060260884
-
G6PD mutations and haplotypes in various ethnic groups
-
in press
-
Xu W, Westwood B, Bartsocas CS, Malcorra-Azpiazu JJ, Indrak K, Beutler E: G6PD mutations and haplotypes in various ethnic groups. Blood 1995 (in press)
-
(1995)
Blood
-
-
Xu, W.1
Westwood, B.2
Bartsocas, C.S.3
Malcorra-Azpiazu, J.J.4
Indrak, K.5
Beutler, E.6
-
220
-
-
84914026518
-
Detection of deficient erythrocyte regeneration of reduced triphosphopyridine nucleotide from glucose-6-phosphate. Evaluation of a rapid screening test
-
Kraus AP, Neely CL, Carey FT, Kraus LM: Detection of deficient erythrocyte regeneration of reduced triphosphopyridine nucleotide from glucose-6-phosphate. Evaluation of a rapid screening test. Ann Intern Med 56:765, 1962
-
(1962)
Ann Intern Med
, vol.56
, pp. 765
-
-
Kraus, A.P.1
Neely, C.L.2
Carey, F.T.3
Kraus, L.M.4
-
221
-
-
0027287495
-
G6PD Mediterranean accounts for the high prevalence of G6PD deficiency in Kurdish Jews
-
Oppenheim A, Jury CL, Rund D, Vulliamy TJ, Luzzatto L: G6PD Mediterranean accounts for the high prevalence of G6PD deficiency in Kurdish Jews. Hum Genet 91:293, 1993
-
(1993)
Hum Genet
, vol.91
, pp. 293
-
-
Oppenheim, A.1
Jury, C.L.2
Rund, D.3
Vulliamy, T.J.4
Luzzatto, L.5
-
222
-
-
0025831986
-
Screening for glucose-6-phosphate dehydrogenase deficiency as a preventive measure: Prevalence among 1,286,000 Greek newborn infants
-
Missiou-Tsagaraki S: Screening for glucose-6-phosphate dehydrogenase deficiency as a preventive measure: Prevalence among 1,286,000 Greek newborn infants. J Pediatr 119:293, 1991
-
(1991)
J Pediatr
, vol.119
, pp. 293
-
-
Missiou-Tsagaraki, S.1
-
223
-
-
36949069869
-
Incidence of the erythrocytic defect associated with drug sensitivity among Oriental subjects
-
Beutler E, Yeh MKY, Necheles T: Incidence of the erythrocytic defect associated with drug sensitivity among Oriental subjects. Nature 183:684, 1959
-
(1959)
Nature
, vol.183
, pp. 684
-
-
Beutler, E.1
Yeh, M.K.Y.2
Necheles, T.3
-
224
-
-
33749998012
-
Investigation of RBC-G6PD deficiency gene frequency in 9 nationality populations in 7 provinces (autonomous region) of China
-
Xu Y: Investigation of RBC-G6PD deficiency gene frequency in 9 nationality populations in 7 provinces (autonomous region) of China. Hered Dis 2:67, 1985
-
(1985)
Hered Dis
, vol.2
, pp. 67
-
-
Xu, Y.1
-
225
-
-
0024238742
-
Glucose-6-phosphate dehydrogenase variants and polymorphic frequency in Guangdong, China
-
Du CS, Xu YK, Hua XY, Wu QL, Liu LB: Glucose-6-phosphate dehydrogenase variants and polymorphic frequency in Guangdong, China. Hum Genet 80:385, 1988
-
(1988)
Hum Genet
, vol.80
, pp. 385
-
-
Du, C.S.1
Xu, Y.K.2
Hua, X.Y.3
Wu, Q.L.4
Liu, L.B.5
-
226
-
-
0000596948
-
G6PD variants in southern Asian populations
-
Yoshida A, Beutler E (eds): Orlando, FL, Academic
-
Panich V: G6PD variants in southern Asian populations, in Yoshida A, Beutler E (eds): Glucose-6-Phosphate Dehydrogenase, Orlando, FL, Academic, 1986, p 195
-
(1986)
Glucose-6-Phosphate Dehydrogenase
, pp. 195
-
-
Panich, V.1
-
227
-
-
0021936916
-
Glucose-6-phosphate dehydrogenase
-
Harris H, Hirschhorn K (eds): New York, NY, Plenum
-
Luzzatto L, Battistuzzi G: Glucose-6-phosphate dehydrogenase, in Harris H, Hirschhorn K (eds): Advances in Human Genetics, New York, NY, Plenum, 1985, p 217
-
(1985)
Advances in Human Genetics
, pp. 217
-
-
Luzzatto, L.1
Battistuzzi, G.2
-
228
-
-
0342432859
-
Diverse characteristics of glucose-6-phosphate dehydrogenase from Greek children
-
Kirkman HN, Doxiadis SA, Valaes T, Tassopoulos N, Brinson AG: Diverse characteristics of glucose-6-phosphate dehydrogenase from Greek children. J Lab Clin Med 65:212, 1965
-
(1965)
J Lab Clin Med
, vol.65
, pp. 212
-
-
Kirkman, H.N.1
Doxiadis, S.A.2
Valaes, T.3
Tassopoulos, N.4
Brinson, A.G.5
-
229
-
-
0018975089
-
Genetic heterogeneity of glucose 6-phosphate dehydrogenase deficiency in Sardinia
-
Testa U, Meloni T, Lania A, Battistuzzi G, Cutillo S, Luzzatto L: Genetic heterogeneity of glucose 6-phosphate dehydrogenase deficiency in Sardinia. Hum Genet 56:99, 1980
-
(1980)
Hum Genet
, vol.56
, pp. 99
-
-
Testa, U.1
Meloni, T.2
Lania, A.3
Battistuzzi, G.4
Cutillo, S.5
Luzzatto, L.6
-
230
-
-
0019441979
-
New genetic variants of glucose-6-phosphate dehydrogenase (G6PD) in Italy
-
Sansone G, Perroni L, Testa U, Mareni C, Luzzatto L: New genetic variants of glucose-6-phosphate dehydrogenase (G6PD) in Italy. Ann Hum Genet 45:97, 1981
-
(1981)
Ann Hum Genet
, vol.45
, pp. 97
-
-
Sansone, G.1
Perroni, L.2
Testa, U.3
Mareni, C.4
Luzzatto, L.5
-
231
-
-
0014490491
-
Characterization of glucose-6-phosphate dehydrogenase variants. II. G6PD Kephalonia, G6PD Attica, and G6PD "Seattle-like" found in Greece
-
Rattazzi MC, Lenzerini L, Khan PM, Luzzatto L: Characterization of glucose-6-phosphate dehydrogenase variants. II. G6PD Kephalonia, G6PD Attica, and G6PD "Seattle-like" found in Greece. Am J Hum Genet 21:154, 1969
-
(1969)
Am J Hum Genet
, vol.21
, pp. 154
-
-
Rattazzi, M.C.1
Lenzerini, L.2
Khan, P.M.3
Luzzatto, L.4
-
232
-
-
0014207886
-
Resolution of genetic variants of human erythrocyte glucose-6-phosphate dehydrogenase by thin layer chromatography
-
Luzzatto L, Okoye VCN: Resolution of genetic variants of human erythrocyte glucose-6-phosphate dehydrogenase by thin layer chromatography. Biochem Biophys Res Commun 29:705, 1967
-
(1967)
Biochem Biophys Res Commun
, vol.29
, pp. 705
-
-
Luzzatto, L.1
Okoye, V.C.N.2
-
235
-
-
0019202534
-
Glucose6-phosphate dehydrogenase deficiency in South Vietnamese
-
Panich V, Bumrungtrakul P, Jitjai C, Kamolmatayalkul S, Khoprasert B, Klaisuvan C, Kongmuang U, Maneechai P, Pornpatkul M, Ruengrairatanaroje P, Piyarat S, Viriyayudhakorn S: Glucose6-phosphate dehydrogenase deficiency in South Vietnamese. Hum Hered 30:361, 1980
-
(1980)
Hum Hered
, vol.30
, pp. 361
-
-
Panich, V.1
Bumrungtrakul, P.2
Jitjai, C.3
Kamolmatayalkul, S.4
Khoprasert, B.5
Klaisuvan, C.6
Kongmuang, U.7
Maneechai, P.8
Pornpatkul, M.9
Ruengrairatanaroje, P.10
Piyarat, S.11
Viriyayudhakorn, S.12
-
236
-
-
0015608279
-
Acute hemolysis in G-6-PD Union (Thai) report on four cases
-
Panich V, Na-Nakorn S: Acute hemolysis in G-6-PD Union (Thai) report on four cases. J Med Assoc Thai 56:241, 1973
-
(1973)
J Med Assoc Thai
, vol.56
, pp. 241
-
-
Panich, V.1
Na-Nakorn, S.2
-
237
-
-
0014508664
-
G-6-PD Bangkok: A new variant found in congenital nonspherocytic hemolytic disease (CNHD)
-
Talalak P, Beutler E: G-6-PD Bangkok: A new variant found in congenital nonspherocytic hemolytic disease (CNHD). Blood 33:772, 1969
-
(1969)
Blood
, vol.33
, pp. 772
-
-
Talalak, P.1
Beutler, E.2
-
238
-
-
0015964829
-
G6PD Heian, a glucose-6-phosphate dehydrogenase variant associated with hemolytic anemia found in Japan
-
Nakai T, Yoshida A: G6PD Heian, a glucose-6-phosphate dehydrogenase variant associated with hemolytic anemia found in Japan. Clin Chim Acta 51:199, 1974
-
(1974)
Clin Chim Acta
, vol.51
, pp. 199
-
-
Nakai, T.1
Yoshida, A.2
-
239
-
-
0015407561
-
G-6-PD Mahidol. The most common glucose-6-phosphate dehydrogenase variant in Thailand
-
Panich V, Sungnate T, Wasi P, Na-Nakorn S: G-6-PD Mahidol. The most common glucose-6-phosphate dehydrogenase variant in Thailand. J Med Assoc Thai 55:576, 1972
-
(1972)
J Med Assoc Thai
, vol.55
, pp. 576
-
-
Panich, V.1
Sungnate, T.2
Wasi, P.3
Na-Nakorn, S.4
-
240
-
-
0014780079
-
Further studies on glucose-6-phosphate dehydrogenase deficiency in Chinese subjects
-
McCurdy PR, Blackwell RQ, Todd D, Tso SC, Tuchinda S: Further studies on glucose-6-phosphate dehydrogenase deficiency in Chinese subjects. J Lab Clin Med 75:788, 1970
-
(1970)
J Lab Clin Med
, vol.75
, pp. 788
-
-
McCurdy, P.R.1
Blackwell, R.Q.2
Todd, D.3
Tso, S.C.4
Tuchinda, S.5
-
241
-
-
0023010381
-
Variants of glucose-6-phosphate dehydrogenase in a Vietnamese population
-
Toncheva D: Variants of glucose-6-phosphate dehydrogenase in a Vietnamese population. Hum Hered 36:348, 1986
-
(1986)
Hum Hered
, vol.36
, pp. 348
-
-
Toncheva, D.1
-
242
-
-
0024455091
-
Molecular heterogeneity of G6PD A
-
Beutler E, Kuhl W, Vives-Corrons J-L, Prchal JT: Molecular heterogeneity of G6PD A-. Blood 74:2550, 1989
-
(1989)
Blood
, vol.74
, pp. 2550
-
-
Beutler, E.1
Kuhl, W.2
Vives-Corrons, J.-L.3
Prchal, J.T.4
-
243
-
-
0024743356
-
Evolution of glucose-6-phosphate dehydrogenase variants A+ and A-. Response
-
Beutler E: Evolution of glucose-6-phosphate dehydrogenase variants A+ and A-. Response. Blood 74:1860, 1989
-
(1989)
Blood
, vol.74
, pp. 1860
-
-
Beutler, E.1
-
244
-
-
0026567018
-
The origin of G6PD polymorphisms in Afro-Americans
-
Kay AC, Kuhl W, Prchal JT, Beutler E: The origin of G6PD polymorphisms in Afro-Americans. Am J Hum Genet 50:394, 1992
-
(1992)
Am J Hum Genet
, vol.50
, pp. 394
-
-
Kay, A.C.1
Kuhl, W.2
Prchal, J.T.3
Beutler, E.4
-
245
-
-
0026002955
-
Polymorphic sites in the African population detected by sequence analysis of the glucose-6-phosphate dehydrogenase gene outline the evolution of the variants A and A
-
Vulliamy TJ, Othman A, Town M, Nathwani A, Falusi AG, Mason PJ, Luzzatto L: Polymorphic sites in the African population detected by sequence analysis of the glucose-6-phosphate dehydrogenase gene outline the evolution of the variants A and A-. Proc Natl Acad Sci USA 88:8568, 1991
-
(1991)
Proc Natl Acad Sci USA
, vol.88
, pp. 8568
-
-
Vulliamy, T.J.1
Othman, A.2
Town, M.3
Nathwani, A.4
Falusi, A.G.5
Mason, P.J.6
Luzzatto, L.7
-
246
-
-
0026879729
-
Both mutations in G6PD A- are necessary to produce the G6PD deficient phenotype
-
Town M, Bautista JM, Mason PJ, Luzzatto L: Both mutations in G6PD A- are necessary to produce the G6PD deficient phenotype. Hum Mol Genet 1:171, 1992
-
(1992)
Hum Mol Genet
, vol.1
, pp. 171
-
-
Town, M.1
Bautista, J.M.2
Mason, P.J.3
Luzzatto, L.4
-
247
-
-
4244036411
-
Diverse point mutations of glucose-6-phoshate dehydrogenase (G6PD) gene in Spanish and Cuban patients with hemolytic anaemia
-
Vives Corrons JL, Rovira A, Pujades MA, Estrada M, Vulliamy TJ: Diverse point mutations of glucose-6-phoshate dehydrogenase (G6PD) gene in Spanish and Cuban patients with hemolytic anaemia. Rev Invest Clin 46:234a, 1994 (suppl)
-
(1994)
Rev Invest Clin
, vol.46
, Issue.SUPPL.
-
-
Vives Corrons, J.L.1
Rovira, A.2
Pujades, M.A.3
Estrada, M.4
Vulliamy, T.J.5
-
249
-
-
0027440263
-
Frequency of glucose-6-phosphate dehydrogenase (G6PD) mutations in Chinese, Filipinos, and Laotians from Hawaii
-
Hsia YE, Miyakawa F, Baltazar J, Ching NSP, Yuen J, Westwood B, Beutler E: Frequency of glucose-6-phosphate dehydrogenase (G6PD) mutations in Chinese, Filipinos, and Laotians from Hawaii. Hum Genet 92:470, 1993
-
(1993)
Hum Genet
, vol.92
, pp. 470
-
-
Hsia, Y.E.1
Miyakawa, F.2
Baltazar, J.3
Ching, N.S.P.4
Yuen, J.5
Westwood, B.6
Beutler, E.7
-
250
-
-
0026591865
-
Glucose-6-phosphate dehydrogenase variants in Hawaii
-
Beutler E, Weslwood B, Kuhl W, Hsia YE: Glucose-6-phosphate dehydrogenase variants in Hawaii. Hum Hered 42:327, 1992
-
(1992)
Hum Hered
, vol.42
, pp. 327
-
-
Beutler, E.1
Weslwood, B.2
Kuhl, W.3
Hsia, Y.E.4
-
251
-
-
0027520218
-
Genetic heterogeneity of glucose-6-phosphate dehydrogenase deficiency revealed by single-strand conformation and sequence analysis
-
Calabr̀o V, Mason PJ, Filosa S, Civitelli D, Cittadella R, Tagarelli A, Martini G, Brancati C, Luzzatto L: Genetic heterogeneity of glucose-6-phosphate dehydrogenase deficiency revealed by single-strand conformation and sequence analysis. Am J Hum Genet 52:527, 1993
-
(1993)
Am J Hum Genet
, vol.52
, pp. 527
-
-
Calabr̀o, V.1
Mason, P.J.2
Filosa, S.3
Civitelli, D.4
Cittadella, R.5
Tagarelli, A.6
Martini, G.7
Brancati, C.8
Luzzatto, L.9
-
252
-
-
85060264622
-
Multiple glucose 6-phosphate dehydrogenase deficient variants correlate with malaria endemicity in the Vanuatu archipelago (South Western Pacific)
-
in press
-
Ganczakowski M, Town M, Kaneko A, Bowden DK, Clegg JB, Luzzatto L: Multiple glucose 6-phosphate dehydrogenase deficient variants correlate with malaria endemicity in the Vanuatu archipelago (South Western Pacific). Am J Hum Genet 1994 (in press)
-
(1994)
Am J Hum Genet
-
-
Ganczakowski, M.1
Town, M.2
Kaneko, A.3
Bowden, D.K.4
Clegg, J.B.5
Luzzatto, L.6
-
253
-
-
15844417289
-
Origin of G6PD polymorphism: Malaria and G6PD deficiency
-
Yoshida A, Beutler E (eds): Orlando,FL, Academic
-
Luzzatto L, O'Brien S, Usanga E, Wanachiwanawin W: Origin of G6PD polymorphism: Malaria and G6PD deficiency, in Yoshida A, Beutler E (eds): Glucose-6-Phosphate Dehydrogenase, Orlando,FL, Academic, 1986, p 181
-
(1986)
Glucose-6-Phosphate Dehydrogenase
, pp. 181
-
-
Luzzatto, L.1
O'Brien, S.2
Usanga, E.3
Wanachiwanawin, W.4
-
254
-
-
0001872496
-
Glucose-6-phosphate dehydrogenase mosaicism: Utilization as cell marker in the study of leiomyomas
-
Linder D, Gartler SM: Glucose-6-phosphate dehydrogenase mosaicism: Utilization as cell marker in the study of leiomyomas. Science 150:67, 1965
-
(1965)
Science
, vol.150
, pp. 67
-
-
Linder, D.1
Gartler, S.M.2
-
255
-
-
0014208048
-
Value of genetic variants of glucose-6-phosphate dehydrogenase in tracing the origin of malignant tumors
-
Beutler E, Collins Z, Irwin LE: Value of genetic variants of glucose-6-phosphate dehydrogenase in tracing the origin of malignant tumors. N Engl J Med 276:389, 1967
-
(1967)
N Engl J Med
, vol.276
, pp. 389
-
-
Beutler, E.1
Collins, Z.2
Irwin, L.E.3
-
256
-
-
0023913693
-
The demonstration of tissue clonality by X-linked enzyme histochemistry
-
Thomas GA, Williams D, Williams ED: The demonstration of tissue clonality by X-linked enzyme histochemistry. J Pathol 155:101, 1988
-
(1988)
J Pathol
, vol.155
, pp. 101
-
-
Thomas, G.A.1
Williams, D.2
Williams, E.D.3
-
257
-
-
0344148914
-
G-6-PD as a marker for tumors
-
Yoshida A, Beutler E (eds): Orlando, FL, Academic
-
Beutler E: G-6-PD as a marker for tumors, in Yoshida A, Beutler E (eds): Glucose-6-Phosphate Dehydrogenase. Orlando, FL, Academic. 1986. p 455
-
(1986)
Glucose-6-Phosphate Dehydrogenase
, pp. 455
-
-
Beutler, E.1
-
258
-
-
0018487548
-
Involvement of the erythroid series in acute myeloid leukemia
-
Beutler E, West C, Johnson C: Involvement of the erythroid series in acute myeloid leukemia. Blood 53:1203, 1979
-
(1979)
Blood
, vol.53
, pp. 1203
-
-
Beutler, E.1
West, C.2
Johnson, C.3
-
259
-
-
0017174101
-
Polycythemia vera: Stem-cell and probable clonal origin of the disease
-
Adamson JW, Fialkow PJ, Murphy S, Prchal JF, Steinmann L: Polycythemia vera: Stem-cell and probable clonal origin of the disease. N Engl J Med 295:913, 1976
-
(1976)
N Engl J Med
, vol.295
, pp. 913
-
-
Adamson, J.W.1
Fialkow, P.J.2
Murphy, S.3
Prchal, J.F.4
Steinmann, L.5
-
260
-
-
0017105982
-
Clonal origin of human tumors
-
Fialkow PJ: Clonal origin of human tumors. Biochim Biophys Acta 458:283, 1976
-
(1976)
Biochim Biophys Acta
, vol.458
, pp. 283
-
-
Fialkow, P.J.1
-
261
-
-
0016184570
-
The origin and development of human tumors studied with cell markers
-
Fialkow PJ: The origin and development of human tumors studied with cell markers. N Engl J Med 291:26, 1974
-
(1974)
N Engl J Med
, vol.291
, pp. 26
-
-
Fialkow, P.J.1
-
262
-
-
0015219368
-
Multiple cell origin of hereditary neurofibromas
-
Fialkow PJ, Sagebiel RW, Gartler SM, Rimoin DL: Multiple cell origin of hereditary neurofibromas. N Engl J Med 284:298, 1971
-
(1971)
N Engl J Med
, vol.284
, pp. 298
-
-
Fialkow, P.J.1
Sagebiel, R.W.2
Gartler, S.M.3
Rimoin, D.L.4
-
263
-
-
0023944602
-
RFLP of the X chromosome-linked glucose-6-phosphate dehydrogenase locus in Blacks
-
Yoshida A, Takizawa T, Prchal JT: RFLP of the X chromosome-linked glucose-6-phosphate dehydrogenase locus in Blacks. Am J Hum Genet 42:872, 1988
-
(1988)
Am J Hum Genet
, vol.42
, pp. 872
-
-
Yoshida, A.1
Takizawa, T.2
Prchal, J.T.3
-
264
-
-
0025275642
-
A PvuII restriction fragment length polymorphism of the glucose-6-phosphate dehydrogenase gene is an African-specific marker
-
Fey MF, Wainscoat JS, Mukwala EC, Falusi AG, Vulliamy TJ, Luzzatto L: A PvuII restriction fragment length polymorphism of the glucose-6-phosphate dehydrogenase gene is an African-specific marker. Hum Genet 84:471, 1990
-
(1990)
Hum Genet
, vol.84
, pp. 471
-
-
Fey, M.F.1
Wainscoat, J.S.2
Mukwala, E.C.3
Falusi, A.G.4
Vulliamy, T.J.5
Luzzatto, L.6
-
265
-
-
0026756752
-
A new polymorphic site in the G6PD gene
-
Beutler E, Westwood B, Sipe B: A new polymorphic site in the G6PD gene. Hum Genet 89:485, 1992
-
(1992)
Hum Genet
, vol.89
, pp. 485
-
-
Beutler, E.1
Westwood, B.2
Sipe, B.3
-
266
-
-
0026538143
-
Glucose-6-phosphate dehydrogenase (G6PD) electrophoretic variants and the PvuII polymorphism in Southern African populations
-
Coetzee MJ, Bartleet SC, Ramsay M, Jenkins T: Glucose-6-phosphate dehydrogenase (G6PD) electrophoretic variants and the PvuII polymorphism in Southern African populations. Hum Genet 89:111, 1992
-
(1992)
Hum Genet
, vol.89
, pp. 111
-
-
Coetzee, M.J.1
Bartleet, S.C.2
Ramsay, M.3
Jenkins, T.4
-
267
-
-
0028216018
-
Molecular characterisation of red cell glucose-6-phosphate dehydrogenase deficiency in North-West Pakistan
-
Saha N, Ramzan M, Tay JSH, Low PS, Basair JB, Khan FM: Molecular characterisation of red cell glucose-6-phosphate dehydrogenase deficiency in North-West Pakistan. Hum Hered 44:85, 1994
-
(1994)
Hum Hered
, vol.44
, pp. 85
-
-
Saha, N.1
Ramzan, M.2
Tay, J.S.H.3
Low, P.S.4
Basair, J.B.5
Khan, F.M.6
-
268
-
-
0025203513
-
The NT 1311 polymorphism of G6PD: G6PD Mediterranean mutation may have originated independently in Europe and Asia
-
Beutler E, Kuhl W: The NT 1311 polymorphism of G6PD: G6PD Mediterranean mutation may have originated independently in Europe and Asia. Am J Hum Genet 47:1008, 1990
-
(1990)
Am J Hum Genet
, vol.47
, pp. 1008
-
-
Beutler, E.1
Kuhl, W.2
-
269
-
-
0026516124
-
Studying X-inactivation
-
Curnutte JT, Hopkins PJ, Kuhl W, Beutler E: Studying X-inactivation. Lancet 339:749, 1992
-
(1992)
Lancet
, vol.339
, pp. 749
-
-
Curnutte, J.T.1
Hopkins, P.J.2
Kuhl, W.3
Beutler, E.4
-
270
-
-
0027454606
-
Transcriptional analysis of the active X-chromosome in normal and clonal hematopoiesis
-
Prchal JT, Guan YL, Prchal JF, Barany F: Transcriptional analysis of the active X-chromosome in normal and clonal hematopoiesis. Blood 81:269, 1993
-
(1993)
Blood
, vol.81
, pp. 269
-
-
Prchal, J.T.1
Guan, Y.L.2
Prchal, J.F.3
Barany, F.4
-
271
-
-
0024420337
-
Malaria and red cell genetic defects
-
Nagel RL, Roth EF Jr: Malaria and red cell genetic defects. Blood 74:1213, 1989
-
(1989)
Blood
, vol.74
, pp. 1213
-
-
Nagel, R.L.1
Roth Jr., E.F.2
-
272
-
-
50549170378
-
Glucose-6-phosphate dehydrogenase deficiency haemolytic disease of the newborn, and malaria
-
Motulsky AG: Glucose-6-phosphate dehydrogenase deficiency haemolytic disease of the newborn, and malaria. Lancet 1:1168, 1961
-
(1961)
Lancet
, vol.1
, pp. 1168
-
-
Motulsky, A.G.1
-
273
-
-
36949071079
-
Favism and thalassaemia in Sardinia and their relationship to malaria
-
Siniscalco M, Bernini L, Latte B, Motulsky AG: Favism and thalassaemia in Sardinia and their relationship to malaria. Nature 190:1179, 1961
-
(1961)
Nature
, vol.190
, pp. 1179
-
-
Siniscalco, M.1
Bernini, L.2
Latte, B.3
Motulsky, A.G.4
-
274
-
-
72849171422
-
Malaria in African children with deficient erythrocyte glucose-6-phosphate dehydrogenase
-
Allison AC, Clyde DF: Malaria in African children with deficient erythrocyte glucose-6-phosphate dehydrogenase. BMJ 1:1346, 1961
-
(1961)
BMJ
, vol.1
, pp. 1346
-
-
Allison, A.C.1
Clyde, D.F.2
-
275
-
-
0027436693
-
G6PD deficiency as protection against falciparum malaria: An epidemiologic critique of population and experimental studies
-
Greene LS: G6PD deficiency as protection against falciparum malaria: An epidemiologic critique of population and experimental studies. Yearbook Phys Anthropol 17:153, 1993 (suppl 36)
-
(1993)
Yearbook Phys Anthropol
, vol.17
, Issue.36 SUPPL.
, pp. 153
-
-
Greene, L.S.1
-
276
-
-
0013872790
-
Population genetics of haemoglobin variants, thalassaemia and G-6-PD deficiency, with particular reference to the malaria hypothesis
-
Siniscalco M, Bernini L, Filippi G, Latte B, Meera-Khan P, Piomelli S, Rattazzi M: Population genetics of haemoglobin variants, thalassaemia and G-6-PD deficiency, with particular reference to the malaria hypothesis. Bull WHO 34:379, 1966
-
(1966)
Bull WHO
, vol.34
, pp. 379
-
-
Siniscalco, M.1
Bernini, L.2
Filippi, G.3
Latte, B.4
Meera-Khan, P.5
Piomelli, S.6
Rattazzi, M.7
-
277
-
-
37049045296
-
A challenge to the concept of selection by malaria in glucose-6-phosphate dehydrogenase deficiency
-
Kidson C, Gorman JG: A challenge to the concept of selection by malaria in glucose-6-phosphate dehydrogenase deficiency. Nature 196:49, 1962
-
(1962)
Nature
, vol.196
, pp. 49
-
-
Kidson, C.1
Gorman, J.G.2
-
278
-
-
0019316869
-
Modified G-6-PD/malaria hypothesis
-
Martin SK: Modified G-6-PD/malaria hypothesis. Lancet 1:51, 1980
-
(1980)
Lancet
, vol.1
, pp. 51
-
-
Martin, S.K.1
-
279
-
-
0024447668
-
Susceptibility to hydrogen peroxide of Plasmodium falciparum infecting glucose-6-phosphate dehydrogenase-deficient erythrocytes
-
Kamchonwongpaisan S, Bunyaratvej A, Wanachiwanawin W, Yuthavong Y: Susceptibility to hydrogen peroxide of Plasmodium falciparum infecting glucose-6-phosphate dehydrogenase-deficient erythrocytes. Parasitology 99:171, 1989
-
(1989)
Parasitology
, vol.99
, pp. 171
-
-
Kamchonwongpaisan, S.1
Bunyaratvej, A.2
Wanachiwanawin, W.3
Yuthavong, Y.4
-
280
-
-
0024791882
-
Deleterious synergistic effects of ascorbate and copper on the development of Plasmodium falciparum: An in vitro study in normal and in G6PD-deficient erythrocytes
-
Marva E, Cohen A, Saltman P, Chevion M, Golenser J: Deleterious synergistic effects of ascorbate and copper on the development of Plasmodium falciparum: An in vitro study in normal and in G6PD-deficient erythrocytes. Int J Parasitol 19:779, 1989
-
(1989)
Int J Parasitol
, vol.19
, pp. 779
-
-
Marva, E.1
Cohen, A.2
Saltman, P.3
Chevion, M.4
Golenser, J.5
-
281
-
-
0023685586
-
The adaptation of Plasmodium falciparum to oxidative stress in G6PD deficient human erythrocytes
-
Roth E Jr, Schulman S: The adaptation of Plasmodium falciparum to oxidative stress in G6PD deficient human erythrocytes. Br J Haematol 70:363, 1988
-
(1988)
Br J Haematol
, vol.70
, pp. 363
-
-
Roth Jr., E.1
Schulman, S.2
-
282
-
-
0021267950
-
Activity of divicine in Plasmodium vincke-intected mice has implications for treatment of favism and epidemiology of G-6-PD deficiency
-
Clark IA, Cowden WB, Hunt NH, Maxwell LE, Mackie EJ: Activity of divicine in Plasmodium vincke-intected mice has implications for treatment of favism and epidemiology of G-6-PD deficiency. Br J Haematol 57:479, 1984
-
(1984)
Br J Haematol
, vol.57
, pp. 479
-
-
Clark, I.A.1
Cowden, W.B.2
Hunt, N.H.3
Maxwell, L.E.4
Mackie, E.J.5
-
283
-
-
0024207231
-
Inhibition of the intraerythrocytic development of Plasmodium falciparum in glucose-6-phosphate dehydrogenase deficient erythrocytes is enhanced by oxidants and by crisis form factor
-
Golenser J, Miller J, Spira DT, Kosower NS, Vande Waa JA, Jensen JB: Inhibition of the intraerythrocytic development of Plasmodium falciparum in glucose-6-phosphate dehydrogenase deficient erythrocytes is enhanced by oxidants and by crisis form factor. Trop Med Parasitol 39:273, 1988
-
(1988)
Trop Med Parasitol
, vol.39
, pp. 273
-
-
Golenser, J.1
Miller, J.2
Spira, D.T.3
Kosower, N.S.4
Vande Waa, J.A.5
Jensen, J.B.6
-
284
-
-
0014212745
-
Glucose-6-phosphate-dehydrogenase deficiency, sickling, and malaria in African children in South Western Nigeria
-
Gilles HM, Fletcher KA, Hendrickse RG, Lindner R, Reddy S, Allan N: Glucose-6-phosphate-dehydrogenase deficiency, sickling, and malaria in African children in South Western Nigeria. Lancet 1:138, 1967
-
(1967)
Lancet
, vol.1
, pp. 138
-
-
Gilles, H.M.1
Fletcher, K.A.2
Hendrickse, R.G.3
Lindner, R.4
Reddy, S.5
Allan, N.6
-
285
-
-
0026846795
-
Prevalence of malaria in Ao Nagas and its association with G6PD and HbE
-
Kar S, Seth S, Seth PK: Prevalence of malaria in Ao Nagas and its association with G6PD and HbE. Hum Biol 64:187, 1992
-
(1992)
Hum Biol
, vol.64
, pp. 187
-
-
Kar, S.1
Seth, S.2
Seth, P.K.3
-
286
-
-
0013951103
-
Effects of glucose-6-phosphate dehydrogenase deficiency upon the host and upon host-drug-malaria parasite interactions
-
Powell R, Brewer GJ, De Gowin R, Carson P: Effects of glucose-6-phosphate dehydrogenase deficiency upon the host and upon host-drug-malaria parasite interactions. Mil Med 131:1039, 1966
-
(1966)
Mil Med
, vol.131
, pp. 1039
-
-
Powell, R.1
Brewer, G.J.2
De Gowin, R.3
Carson, P.4
-
287
-
-
0018741278
-
Severe malaria and glucose-6-phosphate-dehydrogenase deficiency: A reappraisal of the malaria/G-6-PD hypothesis
-
Martin SK, Miller LH, Ailing D, Okoye VC, Esan GJF, Osunkoya BO, Deane M: Severe malaria and glucose-6-phosphate-dehydrogenase deficiency: A reappraisal of the malaria/G-6-PD hypothesis. Lancet 1:524, 1979
-
(1979)
Lancet
, vol.1
, pp. 524
-
-
Martin, S.K.1
Miller, L.H.2
Ailing, D.3
Okoye, V.C.4
Esan, G.J.F.5
Osunkoya, B.O.6
Deane, M.7
-
288
-
-
0015506716
-
Glucose-6-phosphate dehydrogenase and malaria. Greater resistance of females heterozygous for enzyme deficiency and of males with non-deficient variant
-
Bienzle U, Lucas AO, Ayeni O, Luzzatto L: Glucose-6-phosphate dehydrogenase and malaria. Greater resistance of females heterozygous for enzyme deficiency and of males with non-deficient variant. Lancet 1:107, 1972
-
(1972)
Lancet
, vol.1
, pp. 107
-
-
Bienzle, U.1
Lucas, A.O.2
Ayeni, O.3
Luzzatto, L.4
-
289
-
-
0021992793
-
Adaptation of plasmodium falciparum to glucose 6-phosphate dehydrogenase-deficient host red cells by production of parasite-encoded enzyme
-
Usanga EA, Luzzatto L: Adaptation of plasmodium falciparum to glucose 6-phosphate dehydrogenase-deficient host red cells by production of parasite-encoded enzyme. Nature 313:793, 1985
-
(1985)
Nature
, vol.313
, pp. 793
-
-
Usanga, E.A.1
Luzzatto, L.2
-
290
-
-
0025309238
-
Expression and characterization of glucose-6-phosphate dehydrogenase of Plasmodium falciparum
-
Kurdi-Haidar B, Luzzatto L: Expression and characterization of glucose-6-phosphate dehydrogenase of Plasmodium falciparum. Mol Biochem Parasitol 41:83, 1990
-
(1990)
Mol Biochem Parasitol
, vol.41
, pp. 83
-
-
Kurdi-Haidar, B.1
Luzzatto, L.2
-
291
-
-
0014680915
-
Glucose 6-phosphate dehydrogenase deficient red cells: Resistance to infection by malarial parasites
-
Luzzatto L, Usanga EA, Reddy S: Glucose 6-phosphate dehydrogenase deficient red cells: Resistance to infection by malarial parasites. Science 164:839, 1969
-
(1969)
Science
, vol.164
, pp. 839
-
-
Luzzatto, L.1
Usanga, E.A.2
Reddy, S.3
-
292
-
-
0020688752
-
Glucose-6-phosphate dehydrogenase deficiency inhibits in vitro growth of Plasmodium falciparum
-
Roth EF Jr, Raventos-Suarez C, Rinaldi A, Nagel RL: Glucose-6-phosphate dehydrogenase deficiency inhibits in vitro growth of Plasmodium falciparum. Proc Natl Acad Sci USA 80:298, 1983
-
(1983)
Proc Natl Acad Sci USA
, vol.80
, pp. 298
-
-
Roth Jr., E.F.1
Raventos-Suarez, C.2
Rinaldi, A.3
Nagel, R.L.4
-
293
-
-
0022588554
-
Association of red cell glucose-6-phosphate dehydrogenase with haemoglobinopathies
-
Samuel APW, Saha N, Acquaye JK, Omer A, Ganeshaguru K, Hassounh E: Association of red cell glucose-6-phosphate dehydrogenase with haemoglobinopathies. Hum Hered 36:107, 1986
-
(1986)
Hum Hered
, vol.36
, pp. 107
-
-
Samuel, A.P.W.1
Saha, N.2
Acquaye, J.K.3
Omer, A.4
Ganeshaguru, K.5
Hassounh, E.6
-
294
-
-
0015493129
-
Clinical and biochemical interactions of glucose-6-phosphate dehydrogenase deficiency and sickle-cell anemia
-
Piomelli S, Reindorf CA, Arzanian MT, Corash LM: Clinical and biochemical interactions of glucose-6-phosphate dehydrogenase deficiency and sickle-cell anemia. N Engl J Med 287:213, 1972
-
(1972)
N Engl J Med
, vol.287
, pp. 213
-
-
Piomelli, S.1
Reindorf, C.A.2
Arzanian, M.T.3
Corash, L.M.4
-
295
-
-
0018837933
-
Glucose-6-phosphate dehydrogenase deficiency and homozygous sickle cell disease in Jamaica
-
Gibbs WN, Wardle J, Serjeant GR: Glucose-6-phosphate dehydrogenase deficiency and homozygous sickle cell disease in Jamaica. Br J Haematol 45:73, 1980
-
(1980)
Br J Haematol
, vol.45
, pp. 73
-
-
Gibbs, W.N.1
Wardle, J.2
Serjeant, G.R.3
-
296
-
-
0014102297
-
Glucose-6-phosphate dehydrogenase deficiency, the sickling trait, and malaria in Saudi Arab children
-
Gelpi AP: Glucose-6-phosphate dehydrogenase deficiency, the sickling trait, and malaria in Saudi Arab children. Trop Peds 71:138, 1967
-
(1967)
Trop Peds
, vol.71
, pp. 138
-
-
Gelpi, A.P.1
-
297
-
-
0021988956
-
Frequency of glucose-6-phosphate dehydrogenase deficiency in sickle-cell disease
-
Warsy AS: Frequency of glucose-6-phosphate dehydrogenase deficiency in sickle-cell disease. Hum Hered 35:143, 1985
-
(1985)
Hum Hered
, vol.35
, pp. 143
-
-
Warsy, A.S.1
-
298
-
-
7144237440
-
Glucose-6-phosphate dehydrogenase deficiency correlated with S. hemoglobin
-
Lewis RA, Hathorn M: Glucose-6-phosphate dehydrogenase deficiency correlated with S. hemoglobin. Ghana Med J 2:131, 1963
-
(1963)
Ghana Med J
, vol.2
, pp. 131
-
-
Lewis, R.A.1
Hathorn, M.2
-
299
-
-
0016389869
-
Prevalence of glucose-6-phosphate dehydrogenase deficiency in sickle cell disease
-
Beutler E, Johnson C, Powars D, West C: Prevalence of glucose-6-phosphate dehydrogenase deficiency in sickle cell disease. N Engl J Med 290:826, 1974
-
(1974)
N Engl J Med
, vol.290
, pp. 826
-
-
Beutler, E.1
Johnson, C.2
Powars, D.3
West, C.4
-
300
-
-
0023898154
-
The cooperative study of sickle cell diseases: Effects of glucose-6-phosphate dehydrogenase deficiency upon sickle cell anemia
-
Sternberg MH, West MS, Gallagher D, Mentzer WCJ, The cooperative study of sickle cell diseases: Effects of glucose-6-phosphate dehydrogenase deficiency upon sickle cell anemia. Blood 71:748, 1988
-
(1988)
Blood
, vol.71
, pp. 748
-
-
Sternberg, M.H.1
West, M.S.2
Gallagher, D.3
Mentzer, W.C.J.4
-
301
-
-
0016832680
-
Anaemic crisis in sickle cell disease
-
Mann JR, Cotter KP, Walker RA, Bird GW, Stuart J: Anaemic crisis in sickle cell disease. J Clin Pathol 28:341, 1975
-
(1975)
J Clin Pathol
, vol.28
, pp. 341
-
-
Mann, J.R.1
Cotter, K.P.2
Walker, R.A.3
Bird, G.W.4
Stuart, J.5
-
302
-
-
0014493355
-
The hemolytic crisis of sickle cell disease: The role of glucose-6-phosphate dehydrogenase deficiency
-
Smits HL, Oski FA, Brody JI: The hemolytic crisis of sickle cell disease: The role of glucose-6-phosphate dehydrogenase deficiency. J Pediatr 74:544, 1969
-
(1969)
J Pediatr
, vol.74
, pp. 544
-
-
Smits, H.L.1
Oski, F.A.2
Brody, J.I.3
-
304
-
-
0022575959
-
Haematological study in Cabo Delgado province, Mozambique; sickle cell trait and G6PD deficiency
-
Nieuwenhuis F, Wolf B, Bomba A, De Graaf P: Haematological study in Cabo Delgado province, Mozambique; sickle cell trait and G6PD deficiency. Trop Geogr Med 38:183, 1986
-
(1986)
Trop Geogr Med
, vol.38
, pp. 183
-
-
Nieuwenhuis, F.1
Wolf, B.2
Bomba, A.3
De Graaf, P.4
-
305
-
-
0016827689
-
Glucose 6-phosphate dehydrogenase deficiency and sickle cell anemia: Frequency and features of the association in an African community
-
Bienzle U, Sodeinde O, Effiong CE, Luzzatto L: Glucose 6-phosphate dehydrogenase deficiency and sickle cell anemia: Frequency and features of the association in an African community. Blood 46:591, 1975
-
(1975)
Blood
, vol.46
, pp. 591
-
-
Bienzle, U.1
Sodeinde, O.2
Effiong, C.E.3
Luzzatto, L.4
-
306
-
-
0026546207
-
Glucose-6-phosphate dehydrogenase deficiency and sickle cell disease in Brazil
-
Saad STO, Costa FF: Glucose-6-phosphate dehydrogenase deficiency and sickle cell disease in Brazil. Hum Hered 42:125, 1992
-
(1992)
Hum Hered
, vol.42
, pp. 125
-
-
Saad, S.T.O.1
Costa, F.F.2
-
307
-
-
0016365165
-
Glucose-6-phosphate dehydrogenase deficiency in sickle cell anemia
-
Steinberg MH, Dreiling BJ: Glucose-6-phosphate dehydrogenase deficiency in sickle cell anemia. Ann Intern Med 80:217, 1974
-
(1974)
Ann Intern Med
, vol.80
, pp. 217
-
-
Steinberg, M.H.1
Dreiling, B.J.2
-
308
-
-
0013534209
-
The hemolytic effect of primaquine. VI. An in vitro test for sensitivity of erythrocytes to primaquine
-
Beutler E, Dem RJ, Alving AS: The hemolytic effect of primaquine. VI. An in vitro test for sensitivity of erythrocytes to primaquine. J Lab Clin Med 45:40, 1955
-
(1955)
J Lab Clin Med
, vol.45
, pp. 40
-
-
Beutler, E.1
Dem, R.J.2
Alving, A.S.3
-
309
-
-
77049152954
-
Further studies on the properties and assay of glucose-6-phosphate dehydrogenase, and 6-phosphogluconate dehydrogenase of rat liver
-
Clock GE, McLean P: Further studies on the properties and assay of glucose-6-phosphate dehydrogenase, and 6-phosphogluconate dehydrogenase of rat liver. Biochem J 55:400, 1953
-
(1953)
Biochem J
, vol.55
, pp. 400
-
-
Clock, G.E.1
McLean, P.2
-
310
-
-
0014530262
-
Automated fluorometric determination of glucose-6-phosphate dehydrogenase (G 6 PD) and 6-phosphogluconate dehydrogenase (6PGD) activities in red blood cells
-
Tan IK, Whitehead TP: Automated fluorometric determination of glucose-6-phosphate dehydrogenase (G 6 PD) and 6-phosphogluconate dehydrogenase (6PGD) activities in red blood cells. Clin Chem 15:467, 1969
-
(1969)
Clin Chem
, vol.15
, pp. 467
-
-
Tan, I.K.1
Whitehead, T.P.2
-
311
-
-
0018100797
-
Maleimide as a inhibitor in measurement of erythrocyte glucose-6-phosphate dehydrogenase activity
-
Deutsch J: Maleimide as a inhibitor in measurement of erythrocyte glucose-6-phosphate dehydrogenase activity. Clin Chem 24:885, 1978
-
(1978)
Clin Chem
, vol.24
, pp. 885
-
-
Deutsch, J.1
-
313
-
-
0003196490
-
Population genetics of glucose-6-phosphate dehydrogenase deficiency of the red cell
-
Blumberg BS (ed): New York, NY, Grune & Stratton
-
Motulsky AG, Campbell-Kraut JM: Population genetics of glucose-6-phosphate dehydrogenase deficiency of the red cell, in Blumberg BS (ed): Proceedings of the Conference on Genetic Polymorphisms and Geographic Variations in Disease, New York, NY, Grune & Stratton, 1961, p 159
-
(1961)
Proceedings of the Conference on Genetic Polymorphisms and Geographic Variations in Disease
, pp. 159
-
-
Motulsky, A.G.1
Campbell-Kraut, J.M.2
-
314
-
-
0014415945
-
Semiquantitative assay of erythrocyte glucose6-phosphate dehydrogenase activity by a new modification of the Motulsky test
-
Marti HR: Semiquantitative assay of erythrocyte glucose6-phosphate dehydrogenase activity by a new modification of the Motulsky test. Experientia 24:416, 1968
-
(1968)
Experientia
, vol.24
, pp. 416
-
-
Marti, H.R.1
-
315
-
-
0016333241
-
The methylene blue reduction test: Evaluation of a screening method for glucose-6-phosphate dehydrogenase deficiency
-
Gibbs WN: The methylene blue reduction test: Evaluation of a screening method for glucose-6-phosphate dehydrogenase deficiency. Am J Trop Med Hyg 23:1197, 1974
-
(1974)
Am J Trop Med Hyg
, vol.23
, pp. 1197
-
-
Gibbs, W.N.1
-
316
-
-
0346017460
-
The methemoglobin reduction test for primaquine-type sensitivity of erythrocytes
-
Brewer GJ, Tarlov AR, Alving AS: The methemoglobin reduction test for primaquine-type sensitivity of erythrocytes. JAMA 180:386, 1962
-
(1962)
JAMA
, vol.180
, pp. 386
-
-
Brewer, G.J.1
Tarlov, A.R.2
Alving, A.S.3
-
317
-
-
45849110375
-
Test for glucose-6-phosphate dehydrogenase deficiency
-
Rakitzis ET: Test for glucose-6-phosphate dehydrogenase deficiency. Lancet 2:1182, 1964
-
(1964)
Lancet
, vol.2
, pp. 1182
-
-
Rakitzis, E.T.1
-
318
-
-
0015972358
-
Simplified method for G6PD screening using blood collected on filter paper
-
Dow PA, Petteway MB, Alperin JB: Simplified method for G6PD screening using blood collected on filter paper. Am J Pathol 61:333, 1974
-
(1974)
Am J Pathol
, vol.61
, pp. 333
-
-
Dow, P.A.1
Petteway, M.B.2
Alperin, J.B.3
-
319
-
-
0014360532
-
Special modifications of the fluorescent screening method for glucose-6-phosphate dehydrogenase deficiency
-
Beutler E, Mitchell M: Special modifications of the fluorescent screening method for glucose-6-phosphate dehydrogenase deficiency. Blood 32:816, 1968
-
(1968)
Blood
, vol.32
, pp. 816
-
-
Beutler, E.1
Mitchell, M.2
-
320
-
-
0013963946
-
A series of new screening procedures for pyruvate kinase deficiency, glucose-6-phosphate dehydrogenase deficiency, and glutathione reductase deficiency
-
Beutler E: A series of new screening procedures for pyruvate kinase deficiency, glucose-6-phosphate dehydrogenase deficiency, and glutathione reductase deficiency. Blood 28:553, 1966
-
(1966)
Blood
, vol.28
, pp. 553
-
-
Beutler, E.1
-
321
-
-
0018611760
-
International committee for standardization in haematology: Recommended screening test for glucose-6-phosphate dehydrogenase (G-6-PD) deficiency
-
Beutler E, Blume KG, Kaplan JC, Löhr GW, Ramot B, Valentine WN: International committee for standardization in haematology: Recommended screening test for glucose-6-phosphate dehydrogenase (G-6-PD) deficiency. Br J Haematol 43:465, 1979
-
(1979)
Br J Haematol
, vol.43
, pp. 465
-
-
Beutler, E.1
Blume, K.G.2
Kaplan, J.C.3
Löhr, G.W.4
Ramot, B.5
Valentine, W.N.6
-
322
-
-
0023674218
-
Isolation of the aged
-
Beutler E: Isolation of the aged. Blood Cells 14:1, 1988
-
(1988)
Blood Cells
, vol.14
, pp. 1
-
-
Beutler, E.1
-
323
-
-
0015266187
-
A simple laboratory procedure for the recognition of A- (African type) G6PD deficiency in acute haemolytic crisis
-
Ringelhahn B: A simple laboratory procedure for the recognition of A- (African type) G6PD deficiency in acute haemolytic crisis. Clin Chim Acta 36:272, 1972
-
(1972)
Clin Chim Acta
, vol.36
, pp. 272
-
-
Ringelhahn, B.1
-
324
-
-
0014701848
-
Diagnosis of erythrocyte glucose-6-phosphate dehydrogenase deficiency in the negro male despite hemolytic crisis
-
Herz F, Kaplan E, Scheye ES: Diagnosis of erythrocyte glucose-6-phosphate dehydrogenase deficiency in the negro male despite hemolytic crisis. Blood 35:90, 1970
-
(1970)
Blood
, vol.35
, pp. 90
-
-
Herz, F.1
Kaplan, E.2
Scheye, E.S.3
-
325
-
-
84908737304
-
Variants of human glucose-6-phosphate dehydrogenase. Studies of samples from New Guinea
-
Beutler E (ed): New York, NY, Grune & Stratton
-
Kirkman HN, Kidson C, Kennedy M: Variants of human glucose-6-phosphate dehydrogenase. Studies of samples from New Guinea, in Beutler E (ed): Hereditary Disorders of Erythrocyte Metabolism, New York, NY, Grune & Stratton, 1968, p 126
-
(1968)
Hereditary Disorders of Erythrocyte Metabolism
, pp. 126
-
-
Kirkman, H.N.1
Kidson, C.2
Kennedy, M.3
-
326
-
-
38049174327
-
The separation of glucose-6-phosphate dehydrogenase-deficient erythrocytes from the blood of heterozygotes for glucose-6-phosphate dehydrogenase deficiency
-
Beutler E, Baluda MC: The separation of glucose-6-phosphate dehydrogenase-deficient erythrocytes from the blood of heterozygotes for glucose-6-phosphate dehydrogenase deficiency. Lancet 1:189, 1964
-
(1964)
Lancet
, vol.1
, pp. 189
-
-
Beutler, E.1
Baluda, M.C.2
-
327
-
-
45849113716
-
A new technique for the ascertainment of heterozygotes for G-6-PD deficiency
-
Lisbon, Portugal, Karger
-
Beutler E, Dern RJ, Baluda MC: A new technique for the ascertainment of heterozygotes for G-6-PD deficiency. Proceedings of the Ninth Congress of the European Society of Haematology, Lisbon, Portugal, Karger, 1963, p 675
-
(1963)
Proceedings of the Ninth Congress of the European Society of Haematology
, pp. 675
-
-
Beutler, E.1
Dern, R.J.2
Baluda, M.C.3
-
328
-
-
0023023043
-
Kinetic analysis in single, intact cells by microspectrophotometry: Evidence for two populations of erythrocytes in an individual heterozygous for glucosse-6-phosphate dehydrogenase deficiency
-
Ashmun RA, Hultquist DE, Schultz JS: Kinetic analysis in single, intact cells by microspectrophotometry: Evidence for two populations of erythrocytes in an individual heterozygous for glucosse-6-phosphate dehydrogenase deficiency. Am J Hematol 23:311, 1986
-
(1986)
Am J Hematol
, vol.23
, pp. 311
-
-
Ashmun, R.A.1
Hultquist, D.E.2
Schultz, J.S.3
-
329
-
-
78651137502
-
Methemoglobin reduction. Studies of the interaction between cell populations and of the role of methylene blue
-
Beutler E, Baluda MC: Methemoglobin reduction. Studies of the interaction between cell populations and of the role of methylene blue. Blood 22:323, 1963
-
(1963)
Blood
, vol.22
, pp. 323
-
-
Beutler, E.1
Baluda, M.C.2
-
330
-
-
0014286728
-
A tetrazolium-linked cytochemical method for estimation of glucose-6-phosphate dehydrogenase activity in individual erythrocytes: Applications in the study of heterozygotes for glucose-6-phosphate dehydrogenase deficiency
-
Fairbanks VF, Lampe LT: A tetrazolium-linked cytochemical method for estimation of glucose-6-phosphate dehydrogenase activity in individual erythrocytes: Applications in the study of heterozygotes for glucose-6-phosphate dehydrogenase deficiency. Blood 31:589, 1968
-
(1968)
Blood
, vol.31
, pp. 589
-
-
Fairbanks, V.F.1
Lampe, L.T.2
-
331
-
-
0014674354
-
The identification of metabolic errors associated with hemolytic anemia
-
Fairbanks VF, Fernandez MN: The identification of metabolic errors associated with hemolytic anemia. JAMA 208:316, 1969
-
(1969)
JAMA
, vol.208
, pp. 316
-
-
Fairbanks, V.F.1
Fernandez, M.N.2
-
332
-
-
0022726482
-
Cytochemical determination of heterozygous glucose-6-phosphate dehydrogenase deficiency in erythrocytes
-
Vogels IMC, van Noorden CJF, Wolf BHM, Saelman DEM, Tromp A, Schutgens RBH, Weening RS: Cytochemical determination of heterozygous glucose-6-phosphate dehydrogenase deficiency in erythrocytes. Br J Haematol 63:402, 1986
-
(1986)
Br J Haematol
, vol.63
, pp. 402
-
-
Vogels, I.M.C.1
Van Noorden, C.J.F.2
Wolf, B.H.M.3
Saelman, D.E.M.4
Tromp, A.5
Schutgens, R.B.H.6
Weening, R.S.7
-
333
-
-
0021957563
-
Tissue-specific levels of human glucose-6-phosphate dehydrogenase correlate with methylation of specific sites at the 3́ end of the gene
-
Battistuzzi G, D'Urso M, Toniolo D, Persico GM, Luzzatto L: Tissue-specific levels of human glucose-6-phosphate dehydrogenase correlate with methylation of specific sites at the 3́ end of the gene. Proc Natl Acad Sci USA 82:1465, 1985
-
(1985)
Proc Natl Acad Sci USA
, vol.82
, pp. 1465
-
-
Battistuzzi, G.1
D'Urso, M.2
Toniolo, D.3
Persico, G.M.4
Luzzatto, L.5
-
334
-
-
0018906593
-
Glucose-6-phosphate dehydrogenase variants: Reexamination of G6PD Chicago and Cornell and a new variant (G6PD Pea Ridge) resembling G6PD Chicago
-
Fairbanks VF, Nepo AG, Beutler E, Dickson ER, Honig G: Glucose-6-phosphate dehydrogenase variants: Reexamination of G6PD Chicago and Cornell and a new variant (G6PD Pea Ridge) resembling G6PD Chicago. Blood 55:216, 1980
-
(1980)
Blood
, vol.55
, pp. 216
-
-
Fairbanks, V.F.1
Nepo, A.G.2
Beutler, E.3
Dickson, E.R.4
Honig, G.5
-
335
-
-
0025242265
-
Origin and spread of the glucose-6-phosphate dehydrogenase variant (G6PD-Mediterranean) in the Middle East
-
Kurdi-Haidar B, Mason PJ, Berrebi A, Ankra-Badu G, Al-Ali A, Oppenheim A, Luzzatto L: Origin and spread of the glucose-6-phosphate dehydrogenase variant (G6PD-Mediterranean) in the Middle East. Am J Hum Genet 47:1013, 1990
-
(1990)
Am J Hum Genet
, vol.47
, pp. 1013
-
-
Kurdi-Haidar, B.1
Mason, P.J.2
Berrebi, A.3
Ankra-Badu, G.4
Al-Ali, A.5
Oppenheim, A.6
Luzzatto, L.7
-
336
-
-
0026629648
-
Molecular characterization of glucose-6-phosphate dehydrogenase (G6PD) deficiency by natural and amplification created restriction sites: Five mutations account for most G6PD deficiency cases in Taiwan
-
Chang J-G, Chiou S-S, Perng L-I, Chen T-C, Liu T-C, Lee L-S, Chen P-H, Tang TK: Molecular characterization of glucose-6-phosphate dehydrogenase (G6PD) deficiency by natural and amplification created restriction sites: Five mutations account for most G6PD deficiency cases in Taiwan. Blood 80:1079, 1992
-
(1992)
Blood
, vol.80
, pp. 1079
-
-
Chang, J.-G.1
Chiou, S.-S.2
Perng, L.-I.3
Chen, T.-C.4
Liu, T.-C.5
Lee, L.-S.6
Chen, P.-H.7
Tang, T.K.8
-
337
-
-
0026525187
-
Prenatal diagnosis of glucose-6-P dehydrogenase (G6PD) deficiency
-
Beutler E, Kuhl W, Fox M, Tabsh K, Crandall BF: Prenatal diagnosis of glucose-6-P dehydrogenase (G6PD) deficiency. Acta Haematol 87:103, 1992
-
(1992)
Acta Haematol
, vol.87
, pp. 103
-
-
Beutler, E.1
Kuhl, W.2
Fox, M.3
Tabsh, K.4
Crandall, B.F.5
-
339
-
-
0024445936
-
Effect of desferrioxamine B on hemolysis in glucose-6-phosphate dehydrogenase deficiency
-
Khalifa AS, El-Alfy MS, Mokhtar G, Fakeir AA, Khazbak MA, El-Baz F, El-Kholy M: Effect of desferrioxamine B on hemolysis in glucose-6-phosphate dehydrogenase deficiency. Acta Haematol 82:113, 1989
-
(1989)
Acta Haematol
, vol.82
, pp. 113
-
-
Khalifa, A.S.1
El-Alfy, M.S.2
Mokhtar, G.3
Fakeir, A.A.4
Khazbak, M.A.5
El-Baz, F.6
El-Kholy, M.7
-
340
-
-
0015088846
-
The potential use of xylitol in glucose-6-phosphate dehydrogenase deficiency anemia
-
Wang YM, Patterson HJ, Van Eys J: The potential use of xylitol in glucose-6-phosphate dehydrogenase deficiency anemia. J Clin Invest 50:1421, 1971
-
(1971)
J Clin Invest
, vol.50
, pp. 1421
-
-
Wang, Y.M.1
Patterson, H.J.2
Van Eys, J.3
-
341
-
-
85060263637
-
Glucose-6-phosphatdehydrogenase-defekt der erythrozyten und favismus
-
Nowicki L, Martin H, Schubert JCF (eds): Munich, Germany, Lehmanns Verlag
-
Salvidio E, Pannacciulli I, Ajmar F, Garŕe C, Gaetani G, Ghio R. Molinino M, Ravazzolo R: Glucose-6-phosphatdehydrogenase-defekt der erythrozyten und favismus, in Nowicki L, Martin H, Schubert JCF (eds): Haemolyse Haemolytische Erkrankungen, Munich, Germany, Lehmanns Verlag, 1972, p 147
-
(1972)
Haemolyse Haemolytische Erkrankungen
, pp. 147
-
-
Salvidio, E.1
Pannacciulli, I.2
Ajmar, F.3
Garŕe, C.4
Gaetani, G.5
Ghio, R.6
Molinino, M.7
Ravazzolo, R.8
-
342
-
-
0022620545
-
Improved erythrocyte survival with combined vitamin e and selenium therapy in children with glucose-6-phosphate dehydrogenase deficiency and mild chronic hemolysis
-
Hafez M, Amar ES, Zedan M, Hammad H, Sorour AH, El-Desouky ES, Gamil N: Improved erythrocyte survival with combined vitamin E and selenium therapy in children with glucose-6-phosphate dehydrogenase deficiency and mild chronic hemolysis. J Pediatr 108:558, 1986
-
(1986)
J Pediatr
, vol.108
, pp. 558
-
-
Hafez, M.1
Amar, E.S.2
Zedan, M.3
Hammad, H.4
Sorour, A.H.5
El-Desouky, E.S.6
Gamil, N.7
-
343
-
-
0023927271
-
The vitamin E status among glucose-6 phosphate dehydrogenase deficient patients and effectiveness of oral vitamin E
-
Eldamhougy S, Elhelw Z, Yamamah G, Hussein L, Fayyad I, Fawzy D: The vitamin E status among glucose-6 phosphate dehydrogenase deficient patients and effectiveness of oral vitamin E. Int J Vitam Nutr Res 58:184, 1988
-
(1988)
Int J Vitam Nutr Res
, vol.58
, pp. 184
-
-
Eldamhougy, S.1
Elhelw, Z.2
Yamamah, G.3
Hussein, L.4
Fayyad, I.5
Fawzy, D.6
-
344
-
-
0018318510
-
Improved erythrocyte survival with high dose vitamin E in chronic hemolyzing G6PD and glutathione synthetase deficiencies
-
Spielberg SP, Boxer LA, Corash LM, Schulman JD: Improved erythrocyte survival with high dose vitamin E in chronic hemolyzing G6PD and glutathione synthetase deficiencies. Ann Intern Med 90:53, 1978
-
(1978)
Ann Intern Med
, vol.90
, pp. 53
-
-
Spielberg, S.P.1
Boxer, L.A.2
Corash, L.M.3
Schulman, J.D.4
-
345
-
-
0018577112
-
An examination of the role of vitamin E in glucose-6-phosphate dehydrogenase deficiency
-
Newman JG, Newman TB, Bowie LJ, Mendelsohn J: An examination of the role of vitamin E in glucose-6-phosphate dehydrogenase deficiency. Clin Biochem 12:149, 1979
-
(1979)
Clin Biochem
, vol.12
, pp. 149
-
-
Newman, J.G.1
Newman, T.B.2
Bowie, L.J.3
Mendelsohn, J.4
-
346
-
-
0020576949
-
High-dose vitamin E does not decrease the rate of chronic hemolysis in glucose-6-phosphate dehydrogenase deficiency
-
Johnson GJ, Vatassery GT, Finkel B, Allen DW: High-dose vitamin E does not decrease the rate of chronic hemolysis in glucose-6-phosphate dehydrogenase deficiency. N Engl J Med 308:1014, 1983
-
(1983)
N Engl J Med
, vol.308
, pp. 1014
-
-
Johnson, G.J.1
Vatassery, G.T.2
Finkel, B.3
Allen, D.W.4
-
347
-
-
0015807434
-
An Iraqi Jewish family with a new red cell glucose-6-phosphate dehydrogenase variant (Gd-Bagdad) and kernicterus
-
Geerdink RA, Horst R, Staal GEJ: An Iraqi Jewish family with a new red cell glucose-6-phosphate dehydrogenase variant (Gd-Bagdad) and kernicterus. Isr J Med Sci 9:1040, 1973
-
(1973)
Isr J Med Sci
, vol.9
, pp. 1040
-
-
Geerdink, R.A.1
Horst, R.2
Staal, G.E.J.3
-
348
-
-
0027603104
-
Index of suspicion. Case 3. Kernicterus in a baby girl homozygous for glucose-6-phosphate dehydrogenase deficiency
-
Oblender M: Index of suspicion. Case 3. Kernicterus in a baby girl homozygous for glucose-6-phosphate dehydrogenase deficiency. Pediatr Rev 14:191, 193, 1993
-
(1993)
Pediatr Rev
, vol.14
, pp. 191
-
-
Oblender, M.1
-
349
-
-
2442680933
-
Kernicterus in G.-6-P.D.-deficiency
-
Ifekwunigwe AE, Luzzatto L: Kernicterus in G.-6-P.D.-deficiency. Lancet 1:667, 1966
-
(1966)
Lancet
, vol.1
, pp. 667
-
-
Ifekwunigwe, A.E.1
Luzzatto, L.2
-
350
-
-
0004726384
-
Erythrocyte enzyme deficiency in unexplained kerniclerus
-
Doxiadis SA, Fessas P, Valaes T: Erythrocyte enzyme deficiency in unexplained kerniclerus. Lancet 2:44, 1960
-
(1960)
Lancet
, vol.2
, pp. 44
-
-
Doxiadis, S.A.1
Fessas, P.2
Valaes, T.3
-
351
-
-
78651131074
-
Kernicterus bei Mangel an Glukose-6-phosphat-Dehydrogenase der Erythrocyten
-
Schaerer K, Herzka H, Marti HR: Kernicterus bei Mangel an Glukose-6-phosphat-Dehydrogenase der Erythrocyten. Helv Paediatr Acta 2:148, 1963
-
(1963)
Helv Paediatr Acta
, vol.2
, pp. 148
-
-
Schaerer, K.1
Herzka, H.2
Marti, H.R.3
-
352
-
-
0004688325
-
Erythrocyte enzyme deficiency in unexplained kernicterus
-
Panizon F: Erythrocyte enzyme deficiency in unexplained kernicterus. Lancet 2:1093, 1960
-
(1960)
Lancet
, vol.2
, pp. 1093
-
-
Panizon, F.1
-
353
-
-
0016288464
-
Phototherapy for neonatal hyperbilirubinemia in mature newborn infants with erythrocyte G-6-PD deficiency
-
Meloni T, Costa S, Dore A, Cutillo S: Phototherapy for neonatal hyperbilirubinemia in mature newborn infants with erythrocyte G-6-PD deficiency. J Pediatr 85:560, 1974
-
(1974)
J Pediatr
, vol.85
, pp. 560
-
-
Meloni, T.1
Costa, S.2
Dore, A.3
Cutillo, S.4
-
354
-
-
0017744851
-
Phototherapy for neonatal jaundice in erythrocyte glucose-6-phosphate dehydrogenase-deficient infants
-
Tan KL: Phototherapy for neonatal jaundice in erythrocyte glucose-6-phosphate dehydrogenase-deficient infants. Pediatrics 59:1023, 1977
-
(1977)
Pediatrics
, vol.59
, pp. 1023
-
-
Tan, K.L.1
-
355
-
-
0018250153
-
Agar in control of hyperbilirubinemia of full-term newborn infants with erythrocyte G-6-PD deficiency
-
Meloni T, Costa S, Corti R, Cutillo S: Agar in control of hyperbilirubinemia of full-term newborn infants with erythrocyte G-6-PD deficiency. Biol Neonate 34:295, 1978
-
(1978)
Biol Neonate
, vol.34
, pp. 295
-
-
Meloni, T.1
Costa, S.2
Corti, R.3
Cutillo, S.4
-
356
-
-
0014329217
-
Drug induced acute haemolytic anaemia in glucose-6-phosphate dehydrogenase deficiency subjects
-
India
-
Rajkondawar VL, Modi TH, Mishra SN: Drug induced acute haemolytic anaemia in glucose-6-phosphate dehydrogenase deficiency subjects. J Assoc Physicians (India) 16:589, 1968
-
(1968)
J Assoc Physicians
, vol.16
, pp. 589
-
-
Rajkondawar, V.L.1
Modi, T.H.2
Mishra, S.N.3
-
357
-
-
0014054271
-
Treatment of typhoid and paratyphoid fever with furazolidone
-
Omar MES, Wahab MFA: Treatment of typhoid and paratyphoid fever with furazolidone. J Trop Med Hyg 70:43, 1967
-
(1967)
J Trop Med Hyg
, vol.70
, pp. 43
-
-
Omar, M.E.S.1
Wahab, M.F.A.2
-
358
-
-
4444311622
-
Hemolytic anemia following isobutyl nitrate (IBN) inhalation in a patient with glucose-6-phosphate dehydrogenase (G-6-PD) deficiency
-
abstr
-
Little C, Schacter B: Hemolytic anemia following isobutyl nitrate (IBN) inhalation in a patient with glucose-6-phosphate dehydrogenase (G-6-PD) deficiency. Blood 54:34A, 1979 (suppl, abstr)
-
(1979)
Blood
, vol.54
, Issue.SUPPL.
-
-
Little, C.1
Schacter, B.2
-
359
-
-
0024550226
-
Naphthalene-induced hemolysis in a black female toddler deficient in glucose-6-phosphate dehydrogenase
-
Melzer-Lange M, Walsh-Kelly C: Naphthalene-induced hemolysis in a black female toddler deficient in glucose-6-phosphate dehydrogenase. Pediatr Emerg Care 5:24, 1989
-
(1989)
Pediatr Emerg Care
, vol.5
, pp. 24
-
-
Melzer-Lange, M.1
Walsh-Kelly, C.2
-
360
-
-
0026042707
-
Hemolysis from exposure to naphthalene mothballs
-
Todisco V, Lamour J, Finberg L: Hemolysis from exposure to naphthalene mothballs. N Engl J Med 325:1660, 1991
-
(1991)
N Engl J Med
, vol.325
, pp. 1660
-
-
Todisco, V.1
Lamour, J.2
Finberg, L.3
-
361
-
-
0026082596
-
Hemolytic anemia due to G6PD deficiency and urate oxidase in a kidney-transplant patient
-
Ducros J, Saingra S, Rampai M, Coulange C, Barbe M-C, Verzetti G: Hemolytic anemia due to G6PD deficiency and urate oxidase in a kidney-transplant patient. Clin Nephrol 35:89, 1991
-
(1991)
Clin Nephrol
, vol.35
, pp. 89
-
-
Ducros, J.1
Saingra, S.2
Rampai, M.3
Coulange, C.4
Barbe, M.-C.5
Verzetti, G.6
-
362
-
-
0020653181
-
Phenazopyridine-induced hemolytic anemia in a patient with G-6-PD deficiency
-
Tishler M: Phenazopyridine-induced hemolytic anemia in a patient with G-6-PD deficiency. Acta Haematol 70:208, 1983
-
(1983)
Acta Haematol
, vol.70
, pp. 208
-
-
Tishler, M.1
-
363
-
-
0025012469
-
Ascorbic-acid-induced haemolysis in G-6-PD deficiency
-
Mehta JB, Singhal SB, Mehta BC: Ascorbic-acid-induced haemolysis in G-6-PD deficiency. Lancet 336:944, 1990
-
(1990)
Lancet
, vol.336
, pp. 944
-
-
Mehta, J.B.1
Singhal, S.B.2
Mehta, B.C.3
-
365
-
-
0027453215
-
Lesson of the Week: Acute haemolysis induced by high dose ascorbic acid in glucose-6-phosphate dehydrogenase deficiency
-
Rees DC, Kelsey H, Richards JDM: Lesson of the Week: Acute haemolysis induced by high dose ascorbic acid in glucose-6-phosphate dehydrogenase deficiency. BMJ 306:841, 1993
-
(1993)
BMJ
, vol.306
, pp. 841
-
-
Rees, D.C.1
Kelsey, H.2
Richards, J.D.M.3
-
366
-
-
0016076303
-
Platelet-function studies in patients with glucose-6-phosphate dehydrogenase deficiency
-
Schwartz JP, Cooperberg AA, Rosenberg A: Platelet-function studies in patients with glucose-6-phosphate dehydrogenase deficiency. Br J Haematol 27:273, 1974
-
(1974)
Br J Haematol
, vol.27
, pp. 273
-
-
Schwartz, J.P.1
Cooperberg, A.A.2
Rosenberg, A.3
-
367
-
-
15844392075
-
Comparative studies on human blood platelets of normal and glucose-6-phosphate-dehydrogenase-deficient donors
-
Spangenberg P, Bosia A, Arese P, Losche W, Till U: Comparative studies on human blood platelets of normal and glucose-6-phosphate-dehydrogenase-deficient donors. Acta Biol Med Ger 41:25, 1982
-
(1982)
Acta Biol Med Ger
, vol.41
, pp. 25
-
-
Spangenberg, P.1
Bosia, A.2
Arese, P.3
Losche, W.4
Till, U.5
-
369
-
-
0014850267
-
Loss of flaps due to glucose-6-phosphate dehydrogenase deficiency
-
Adamson JE, Taddeo RJ, Gwyn PP: Loss of flaps due to glucose-6-phosphate dehydrogenase deficiency. Plast Reconstr Surg 46:301, 1970
-
(1970)
Plast Reconstr Surg
, vol.46
, pp. 301
-
-
Adamson, J.E.1
Taddeo, R.J.2
Gwyn, P.P.3
-
370
-
-
0016271520
-
Possible incompatibility of glucose-6-phosphate dehydrogenase deficiency and championship athletic performance
-
Petrakis NL, Petrakis SJ, Wiesenfeld SL, Spanidou E: Possible incompatibility of glucose-6-phosphate dehydrogenase deficiency and championship athletic performance. Med Sci Sports Exerc 6:191, 1974
-
(1974)
Med Sci Sports Exerc
, vol.6
, pp. 191
-
-
Petrakis, N.L.1
Petrakis, S.J.2
Wiesenfeld, S.L.3
Spanidou, E.4
-
371
-
-
0013963697
-
Anemia, cataracts, and seizures in patient with glucose-6-phosphate dehydrogenase deficiency
-
Westring DW, Pisciotta AV: Anemia, cataracts, and seizures in patient with glucose-6-phosphate dehydrogenase deficiency. Arch Intern Med 118:385, 1966
-
(1966)
Arch Intern Med
, vol.118
, pp. 385
-
-
Westring, D.W.1
Pisciotta, A.V.2
-
372
-
-
0014944473
-
Epilepsy and G-6-PD deficiency
-
Elian M: Epilepsy and G-6-PD deficiency. Lancet 1:364, 1970
-
(1970)
Lancet
, vol.1
, pp. 364
-
-
Elian, M.1
-
373
-
-
0018179174
-
Glucose-6-phosphate dehydrogenase variants: Gd (+) Alexandra associated with neonatal jaundice and Gd (-) Camperdown in a young man with lamellar cataracts
-
Harley JD, Agar NS, Yoshida A: Glucose-6-phosphate dehydrogenase variants: Gd (+) Alexandra associated with neonatal jaundice and Gd (-) Camperdown in a young man with lamellar cataracts. J Lab Clin Med 91:295, 1978
-
(1978)
J Lab Clin Med
, vol.91
, pp. 295
-
-
Harley, J.D.1
Agar, N.S.2
Yoshida, A.3
-
374
-
-
17144469595
-
Kongenitale nichtspharozytare hamolytische An̈amie, Katarakt und Glucose-6-phosphat-dehydrogenase-mangel
-
Helge H, Borner K: Kongenitale nichtspharozytare hamolytische An̈amie, Katarakt und Glucose-6-phosphat-dehydrogenase-mangel. Dtsch Med Wochenschr 91:1584, 1966
-
(1966)
Dtsch Med Wochenschr
, vol.91
, pp. 1584
-
-
Helge, H.1
Borner, K.2
-
375
-
-
0016849919
-
Cataracts with a glucose-6-phosphate dehydrogenase variant
-
Harley JD, Agar NS, Gruca MA: Cataracts with a glucose-6-phosphate dehydrogenase variant. BMJ 2:86, 1975
-
(1975)
BMJ
, vol.2
, pp. 86
-
-
Harley, J.D.1
Agar, N.S.2
Gruca, M.A.3
-
376
-
-
0019351118
-
Increased incidence of cataract in male subjects deficient in glucose-6-phosphate dehydrogenase
-
Orzalesi N, Sorcinelli R, Guiso G: Increased incidence of cataract in male subjects deficient in glucose-6-phosphate dehydrogenase. Arch Ophthalmol 99:69, 1981
-
(1981)
Arch Ophthalmol
, vol.99
, pp. 69
-
-
Orzalesi, N.1
Sorcinelli, R.2
Guiso, G.3
-
377
-
-
0025642482
-
Glucose 6-phosphate dehydrogenase deficiency and cataract of patients in Northern Sardinia
-
Meloni T, Carta F, Forteleoni G, Carta A, Ena F, Meloni GF: Glucose 6-phosphate dehydrogenase deficiency and cataract of patients in Northern Sardinia. Am J Ophthalmol 110:661, 1990
-
(1990)
Am J Ophthalmol
, vol.110
, pp. 661
-
-
Meloni, T.1
Carta, F.2
Forteleoni, G.3
Carta, A.4
Ena, F.5
Meloni, G.F.6
-
378
-
-
0025567036
-
Senile cataract and glucose-6-phosphate dehydrogenase deficiency in Indians
-
Bhatia RPS, Patel R, Dubey B: Senile cataract and glucose-6-phosphate dehydrogenase deficiency in Indians. Trop Geogr Med 42:349, 1990
-
(1990)
Trop Geogr Med
, vol.42
, pp. 349
-
-
Bhatia, R.P.S.1
Patel, R.2
Dubey, B.3
-
379
-
-
0018819389
-
G 6 PD deficiency in senile cataracts
-
Panich V, Na-Nakorn S: G 6 PD deficiency in senile cataracts. Hum Genet 55:123, 1980
-
(1980)
Hum Genet
, vol.55
, pp. 123
-
-
Panich, V.1
Na-Nakorn, S.2
-
380
-
-
3042535967
-
Studies on the correlation of the genetically determined trait, glucose-6-phosphate dehydrogenase deficiency, with behavioral manifestations in schizophrenia
-
Dern RJ, Glynn MF, Brewer GJ: Studies on the correlation of the genetically determined trait, glucose-6-phosphate dehydrogenase deficiency, with behavioral manifestations in schizophrenia. J Lab Clin Med 62:319, 1963
-
(1963)
J Lab Clin Med
, vol.62
, pp. 319
-
-
Dern, R.J.1
Glynn, M.F.2
Brewer, G.J.3
-
381
-
-
3042538357
-
A re-evaluation of the relationship between glucose-6-phosphate dehydrogenase deficiency and the behavioral manifestations of schizophrenia
-
Bowman JE, Brewer GJ, Frischer H, Carter JL, Eisenstein RB, Bayrakci C: A re-evaluation of the relationship between glucose-6-phosphate dehydrogenase deficiency and the behavioral manifestations of schizophrenia. J Lab Clin Med 65:222, 1965
-
(1965)
J Lab Clin Med
, vol.65
, pp. 222
-
-
Bowman, J.E.1
Brewer, G.J.2
Frischer, H.3
Carter, J.L.4
Eisenstein, R.B.5
Bayrakci, C.6
-
382
-
-
0017190789
-
Impaired renin release after repetitive upright stimulation in G-6-PD deficiency subjects
-
Rappelli A, Glorioso N, Tedde R, Madeddu P, Campus S: Impaired renin release after repetitive upright stimulation in G-6-PD deficiency subjects. IRCS 4:423, 1976
-
(1976)
IRCS
, vol.4
, pp. 423
-
-
Rappelli, A.1
Glorioso, N.2
Tedde, R.3
Madeddu, P.4
Campus, S.5
-
383
-
-
2042487130
-
Abnormal oral glucose tolerance response in erythrocyte glucose-6-phosphate dehydrogenase deficiency
-
Chanmugam D, Frumin AM: Abnormal oral glucose tolerance response in erythrocyte glucose-6-phosphate dehydrogenase deficiency. N Engl J Med 271:1202, 1964
-
(1964)
N Engl J Med
, vol.271
, pp. 1202
-
-
Chanmugam, D.1
Frumin, A.M.2
-
384
-
-
0025863734
-
Glucose-6-phosphate dehydrogenase deficiency and diabetes mellitus
-
Niazi GA: Glucose-6-phosphate dehydrogenase deficiency and diabetes mellitus. Int J Hematol 54:295, 1991
-
(1991)
Int J Hematol
, vol.54
, pp. 295
-
-
Niazi, G.A.1
-
385
-
-
0014023543
-
Oral glucose tolerance in negro men deficient in G-6-PD
-
Eppes R, Brewer G, De Gowin R, McNamara J, Flanagan C, Schrier S, Tarlov A, Powell R, Carson P: Oral glucose tolerance in negro men deficient in G-6-PD. N Engl J Med 275:855, 1966
-
(1966)
N Engl J Med
, vol.275
, pp. 855
-
-
Eppes, R.1
Brewer, G.2
De Gowin, R.3
McNamara, J.4
Flanagan, C.5
Schrier, S.6
Tarlov, A.7
Powell, R.8
Carson, P.9
-
386
-
-
0025907130
-
Insulin secretion in patients deficient in glucose-6-phosphate dehydrogenase
-
Monte Alegre S, Saad STO, Delatre E, Saad MJA: Insulin secretion in patients deficient in glucose-6-phosphate dehydrogenase. Horm Metab Res 23:171, 1991
-
(1991)
Horm Metab Res
, vol.23
, pp. 171
-
-
Monte Alegre, S.1
Saad, S.T.O.2
Delatre, E.3
Saad, M.J.A.4
-
387
-
-
0026465886
-
G6PD deficiency and diabetes mellitus in northern Sardinian subjects
-
Meloni T, Pacifico A, Forteleoni G, Meloni GF: G6PD deficiency and diabetes mellitus in northern Sardinian subjects. Haematologica 77:94, 1992
-
(1992)
Haematologica
, vol.77
, pp. 94
-
-
Meloni, T.1
Pacifico, A.2
Forteleoni, G.3
Meloni, G.F.4
-
388
-
-
0025739057
-
Cortisol levels in glucose-6-phosphate dehydrogenase deficiency
-
Saad MJA, Monte-Alegre S, Saad STO: Cortisol levels in glucose-6-phosphate dehydrogenase deficiency. Horm Res 35:1, 1991
-
(1991)
Horm Res
, vol.35
, pp. 1
-
-
Saad, M.J.A.1
Monte-Alegre, S.2
Saad, S.T.O.3
-
389
-
-
0015844068
-
Cortisol metabolism in glucose-6-phosphate dehydrogenase deficiency
-
So PL, Chan TK, Lam SK, Teng CS, Yeung RTT, Todd D: Cortisol metabolism in glucose-6-phosphate dehydrogenase deficiency. Metabolism 22:1443, 1973
-
(1973)
Metabolism
, vol.22
, pp. 1443
-
-
So, P.L.1
Chan, T.K.2
Lam, S.K.3
Teng, C.S.4
Yeung, R.T.T.5
Todd, D.6
-
390
-
-
0014967669
-
Elevated blood pressure, pulse rate and serum creatinine in negro males deficient in glucose-6-phosphate dehydrogenase
-
Wiesenfeld SL, Petrakis NL, Sams BJ, Collen MF, Cutler JL: Elevated blood pressure, pulse rate and serum creatinine in negro males deficient in glucose-6-phosphate dehydrogenase. N Engl J Med 282:1001, 1970
-
(1970)
N Engl J Med
, vol.282
, pp. 1001
-
-
Wiesenfeld, S.L.1
Petrakis, N.L.2
Sams, B.J.3
Collen, M.F.4
Cutler, J.L.5
-
391
-
-
0025135246
-
Blood pressure and other cardiovascular disease risk factors in black adults with sickle cell trait or glucose-6-phosphate dehydrogenase deficiency
-
Nwankwo MU, Bunker CH, Ukoli FA, Omene JA, Freeman DT, Vergis EN, Yen LL, Kuller LH: Blood pressure and other cardiovascular disease risk factors in black adults with sickle cell trait or glucose-6-phosphate dehydrogenase deficiency. Genet Epidemiol 7:211, 1990
-
(1990)
Genet Epidemiol
, vol.7
, pp. 211
-
-
Nwankwo, M.U.1
Bunker, C.H.2
Ukoli, F.A.3
Omene, J.A.4
Freeman, D.T.5
Vergis, E.N.6
Yen, L.L.7
Kuller, L.H.8
-
392
-
-
0025849726
-
Increased prevalence of glucose-6-phosphate dehydrogenase deficiency in patients with cholelithiasis
-
Meloni T, Forteleoni G, Noja G, Dettori G, Sale MA, Meloni GF: Increased prevalence of glucose-6-phosphate dehydrogenase deficiency in patients with cholelithiasis. Acta Haematol 85:76, 1991
-
(1991)
Acta Haematol
, vol.85
, pp. 76
-
-
Meloni, T.1
Forteleoni, G.2
Noja, G.3
Dettori, G.4
Sale, M.A.5
Meloni, G.F.6
-
393
-
-
0026406803
-
844c: A study on its expression in blood cells and muscle
-
844c: A study on its expression in blood cells and muscle. Enzyme 45:180, 1991
-
(1991)
Enzyme
, vol.45
, pp. 180
-
-
Ninfali, P.1
Bresolin, N.2
Baronciani, L.3
Fortunato, F.4
Comi, G.5
Magnani, M.6
Scarlato, G.7
-
394
-
-
0024658143
-
Muscle glucose-6-phosphate dehydrogenase deficiency
-
Bresolin N, Bet L, Moggio M, Meola G, Fortunato F, Comi G, Adobbati L, Geremia L, Pittalis S, Scarlato G: Muscle glucose-6-phosphate dehydrogenase deficiency. J Neurol 236:193, 1989
-
(1989)
J Neurol
, vol.236
, pp. 193
-
-
Bresolin, N.1
Bet, L.2
Moggio, M.3
Meola, G.4
Fortunato, F.5
Comi, G.6
Adobbati, L.7
Geremia, L.8
Pittalis, S.9
Scarlato, G.10
-
395
-
-
0024604628
-
Incidence and causes of sepsis in glucose-6-phosphate dehydrogenase-deficient newborn infants
-
Abu-Osba YK, Mallouh AA, Harm RW: Incidence and causes of sepsis in glucose-6-phosphate dehydrogenase-deficient newborn infants. J Pediatr 114:748, 1989
-
(1989)
J Pediatr
, vol.114
, pp. 748
-
-
Abu-Osba, Y.K.1
Mallouh, A.A.2
Harm, R.W.3
-
396
-
-
0023573249
-
Glucose-6-phosphate dehydrogenase deficiency, neutrophil dysfunction and Chromobacterium violaceum sepsis
-
Mamlok RJ, Mamlok V, Mills GC, Daeschner CW, III, Schmalstieg FC, Anderson DC: Glucose-6-phosphate dehydrogenase deficiency, neutrophil dysfunction and Chromobacterium violaceum sepsis. J Pediatr 111:852, 1987
-
(1987)
J Pediatr
, vol.111
, pp. 852
-
-
Mamlok, R.J.1
Mamlok, V.2
Mills, G.C.3
Daeschner III, C.W.4
Schmalstieg, F.C.5
Anderson, D.C.6
-
397
-
-
0020518594
-
Functional analysis of polymorphonuclear leukocytes in siblings of glucose-6-phosphate dehydrogenase deficiency
-
Matsuura R, Kishi T, Okahata H, Kobayashi M, Tanabe A, Sakura N, Sawano K, Usui T: Functional analysis of polymorphonuclear leukocytes in siblings of glucose-6-phosphate dehydrogenase deficiency. Hiroshima J Med Sci 32:173, 1983
-
(1983)
Hiroshima J Med Sci
, vol.32
, pp. 173
-
-
Matsuura, R.1
Kishi, T.2
Okahata, H.3
Kobayashi, M.4
Tanabe, A.5
Sakura, N.6
Sawano, K.7
Usui, T.8
-
398
-
-
0014034838
-
Associations between red cell glucose-6-phosphate dehydrogenase variants and vascular diseases
-
Long WK, Wilson SW, Frenkel EP: Associations between red cell glucose-6-phosphate dehydrogenase variants and vascular diseases. Am J Hum Genet 19:35, 1967
-
(1967)
Am J Hum Genet
, vol.19
, pp. 35
-
-
Long, W.K.1
Wilson, S.W.2
Frenkel, E.P.3
-
399
-
-
84921001820
-
Neutrophil dysfunction, chronic granulomatous disease, and nonspherocytic haemolytic anaemia caused by complete deficiency of glucose-6-phosphate dehydrogenase
-
Gray GR, Klebanoff SJ, Stamatoyannopoulos G, Austin T, Naiman SC, Yoshida A, Kliman MR, Robinson GCF: Neutrophil dysfunction, chronic granulomatous disease, and nonspherocytic haemolytic anaemia caused by complete deficiency of glucose-6-phosphate dehydrogenase. Lancet 2:530, 1973
-
(1973)
Lancet
, vol.2
, pp. 530
-
-
Gray, G.R.1
Klebanoff, S.J.2
Stamatoyannopoulos, G.3
Austin, T.4
Naiman, S.C.5
Yoshida, A.6
Kliman, M.R.7
Robinson, G.C.F.8
-
400
-
-
0017196031
-
Leukocyte function and characterization of leukocyte glucose-6-phosphate dehydrogenase in Sicilian mutants
-
Schiliro G, Russo A, Mauro L, Pizzarelli G, Marino S: Leukocyte function and characterization of leukocyte glucose-6-phosphate dehydrogenase in Sicilian mutants. Pediatr Res 10:739, 1976
-
(1976)
Pediatr Res
, vol.10
, pp. 739
-
-
Schiliro, G.1
Russo, A.2
Mauro, L.3
Pizzarelli, G.4
Marino, S.5
-
401
-
-
0026871199
-
Increased morbidity following acute viral hepatitis in children with glucose-6-phosphate dehydrogenase deficiency
-
Choudhry VP, Bagga A, Desai N: Increased morbidity following acute viral hepatitis in children with glucose-6-phosphate dehydrogenase deficiency. J Trop Pediatr 38:139, 1992
-
(1992)
J Trop Pediatr
, vol.38
, pp. 139
-
-
Choudhry, V.P.1
Bagga, A.2
Desai, N.3
-
402
-
-
0019830255
-
Glucose-6-phosphate dehydrogenase deficiency and mental retardation
-
Seth PK, Devi ST, Seth S: Glucose-6-phosphate dehydrogenase deficiency and mental retardation. J Inherited Metab Dis 4:93, 1981
-
(1981)
J Inherited Metab Dis
, vol.4
, pp. 93
-
-
Seth, P.K.1
Devi, S.T.2
Seth, S.3
-
403
-
-
0025092157
-
Serum lipoprotein profile and concentration of dehydroepiandrosterone sulfate (DHEAS) in glucose-6-phosphate dehydrogenase-deficient subjects
-
Sheriff DS, El Fakhri M: Serum lipoprotein profile and concentration of dehydroepiandrosterone sulfate (DHEAS) in glucose-6-phosphate dehydrogenase-deficient subjects. Clin Chem 36:393, 1990
-
(1990)
Clin Chem
, vol.36
, pp. 393
-
-
Sheriff, D.S.1
El Fakhri, M.2
-
404
-
-
0026042503
-
A to G substitution identified in exon 2 of the G6PD gene among G6PD deficient Chinese
-
Chao L, Du C-S, Louie E, Zuo L, Chen E, Lubin B, Chiu DTY: A to G substitution identified in exon 2 of the G6PD gene among G6PD deficient Chinese. Nucleic Acids Res 19:6056, 1991
-
(1991)
Nucleic Acids Res
, vol.19
, pp. 6056
-
-
Chao, L.1
Du, C.-S.2
Louie, E.3
Zuo, L.4
Chen, E.5
Lubin, B.6
Chiu, D.T.Y.7
-
405
-
-
0025764346
-
Deficiency in red blood cells
-
MacDonald D, Town M, Mason P, Vulliamy T, Luzzatto L, Goff DK: Deficiency in red blood cells. Nature 350:115, 1991
-
(1991)
Nature
, vol.350
, pp. 115
-
-
MacDonald, D.1
Town, M.2
Mason, P.3
Vulliamy, T.4
Luzzatto, L.5
Goff, D.K.6
-
406
-
-
0027537149
-
G6PD Aures: A new mutation (48 Ile->Thr) causing mild G6PD deficiency is associated with favism
-
Nafa K, Reghis A, Osmani N, Baghli L, Benabadji M, Kaplan J-C, Vulliamy TJ, Luzzatto L: G6PD Aures: A new mutation (48 Ile->Thr) causing mild G6PD deficiency is associated with favism. Hum Mol Genet 2:81, 1993
-
(1993)
Hum Mol Genet
, vol.2
, pp. 81
-
-
Nafa, K.1
Reghis, A.2
Osmani, N.3
Baghli, L.4
Benabadji, M.5
Kaplan, J.-C.6
Vulliamy, T.J.7
Luzzatto, L.8
-
407
-
-
0344985724
-
Diverse point mutations in the human glucose 6-phosphate dehydrogenase gene cause enzyme deficiency and mild or severe hemolytic anemia
-
Vulliamy TJ, D'Urso M, Battistuzzi G, Estrada M, Foulkes NS, Martini G, Calabro V, Poggi V, Giordano R, Town M, Luzzatto L, Persico MG: Diverse point mutations in the human glucose 6-phosphate dehydrogenase gene cause enzyme deficiency and mild or severe hemolytic anemia. Proc Natl Acad Sci USA 85:5171, 1988
-
(1988)
Proc Natl Acad Sci USA
, vol.85
, pp. 5171
-
-
Vulliamy, T.J.1
D'Urso, M.2
Battistuzzi, G.3
Estrada, M.4
Foulkes, N.S.5
Martini, G.6
Calabro, V.7
Poggi, V.8
Giordano, R.9
Town, M.10
Luzzatto, L.11
Persico, M.G.12
-
408
-
-
0025974411
-
Some Mexican glucose-6-phosphate dehydrogenase (G-6-PD) variants revisited
-
Beutler E, Kuhl W, Ramirez E, Lisker R: Some Mexican glucose-6-phosphate dehydrogenase (G-6-PD) variants revisited. Hum Genet 86:371, 1991
-
(1991)
Hum Genet
, vol.86
, pp. 371
-
-
Beutler, E.1
Kuhl, W.2
Ramirez, E.3
Lisker, R.4
-
409
-
-
85060263193
-
-
unpublished observations, January
-
Beutler E, Kuhl W: unpublished observations, January 1991
-
(1991)
-
-
Beutler, E.1
Kuhl, W.2
-
410
-
-
0028098230
-
G6PD Ferrara I has the same two mutations as G6PD A(-) but a distinct biochemical phenotype
-
Cappellini MD, Sampietro M, Toniolo D, Carandina G, Martinez di Montemuros F, Tavazzi D, Fiorelli G: G6PD Ferrara I has the same two mutations as G6PD A(-) but a distinct biochemical phenotype. Hum Genet 93:139, 1994
-
(1994)
Hum Genet
, vol.93
, pp. 139
-
-
Cappellini, M.D.1
Sampietro, M.2
Toniolo, D.3
Carandina, G.4
Martinez Di Montemuros, F.5
Tavazzi, D.6
Fiorelli, G.7
-
411
-
-
0027250301
-
Molecular abnormality of G6PD Konan and G6PD Ube, the most common glucose-6-phosphate dehydrogenase variants in Japan
-
Hirono A, Fujii H, Miwa S: Molecular abnormality of G6PD Konan and G6PD Ube, the most common glucose-6-phosphate dehydrogenase variants in Japan. Hum Genet 91:507, 1993
-
(1993)
Hum Genet
, vol.91
, pp. 507
-
-
Hirono, A.1
Fujii, H.2
Miwa, S.3
-
412
-
-
0027202606
-
Molecular analysis of G6PD variants in northern Italy: A study on the population from the Ferrara district
-
Ninfali P, Baronciani L, Ruzzo A, Fortini C, Amadori E, Dall'ara G, Magnani M, Beutler E: Molecular analysis of G6PD variants in northern Italy: A study on the population from the Ferrara district. Hum Genet 92:139, 1993
-
(1993)
Hum Genet
, vol.92
, pp. 139
-
-
Ninfali, P.1
Baronciani, L.2
Ruzzo, A.3
Fortini, C.4
Amadori, E.5
Dall'ara, G.6
Magnani, M.7
Beutler, E.8
-
413
-
-
0026655456
-
Molecular abnormalities of a human glucose-6-phosphate dehydrogenase variant associated with undetectable enzyme activity and immunologically cross-reacting material
-
Maeda M, Constantoulakis P, Chen C-S, Stamatoyannopoulos G, Yoshida A: Molecular abnormalities of a human glucose-6-phosphate dehydrogenase variant associated with undetectable enzyme activity and immunologically cross-reacting material. Am J Hum Genet 51:386, 1992
-
(1992)
Am J Hum Genet
, vol.51
, pp. 386
-
-
Maeda, M.1
Constantoulakis, P.2
Chen, C.-S.3
Stamatoyannopoulos, G.4
Yoshida, A.5
-
414
-
-
0027547019
-
Molecular characterization of glucose-6-phosphate dehydrogenase (G6PD) variants from Brazil
-
Weimer TA, Salzano FM, Westwood B, Beutler E: Molecular characterization of glucose-6-phosphate dehydrogenase (G6PD) variants from Brazil. Hum Biol 65:41, 1993
-
(1993)
Hum Biol
, vol.65
, pp. 41
-
-
Weimer, T.A.1
Salzano, F.M.2
Westwood, B.3
Beutler, E.4
-
415
-
-
0023446213
-
A single nucleotide base transition is the basis of the common human glucose-6-phosphate dehydrogenase variant A(+)
-
Takizawa T, Yoneyama Y, Miwa S, Yoshida A: A single nucleotide base transition is the basis of the common human glucose-6-phosphate dehydrogenase variant A(+). Genomics 1:228, 1987
-
(1987)
Genomics
, vol.1
, pp. 228
-
-
Takizawa, T.1
Yoneyama, Y.2
Miwa, S.3
Yoshida, A.4
-
416
-
-
0027468461
-
Molecular characterization of glucose-6-phosphatc dehydrogenase (G6PD) deficiency in patients of Chinese descent and identification of new base substitutions in the human G6PD gene
-
Chiu DTY, Zuo L, Chao L, Chen E, Louie E, Lubin B, Liu TZ, Du CS: Molecular characterization of glucose-6-phosphatc dehydrogenase (G6PD) deficiency in patients of Chinese descent and identification of new base substitutions in the human G6PD gene. Blood 81:2150, 1993
-
(1993)
Blood
, vol.81
, pp. 2150
-
-
Chiu, D.T.Y.1
Zuo, L.2
Chao, L.3
Chen, E.4
Louie, E.5
Lubin, B.6
Liu, T.Z.7
Du, C.S.8
-
417
-
-
0024360344
-
G6PD Mahidol, a common deficient variant in South East Asia is caused by a (163)glycine→serine mutation
-
Vulliamy TJ, Wanachiwanawin W, Mason PJ, Luzzatto L: G6PD Mahidol, a common deficient variant in South East Asia is caused by a (163)glycine→serine mutation. Nucleic Acids Res 17:5868, 1989
-
(1989)
Nucleic Acids Res
, vol.17
, pp. 5868
-
-
Vulliamy, T.J.1
Wanachiwanawin, W.2
Mason, P.J.3
Luzzatto, L.4
-
418
-
-
0027259193
-
Variants of glucose-6-phosphate dehydrogenase are due to missense mutations spread throughout the coding region of the gene
-
Vulliamy T, Beutler E, Luzzatto L: Variants of glucose-6-phosphate dehydrogenase are due to missense mutations spread throughout the coding region of the gene. Hum Mutat 2:159, 1993
-
(1993)
Hum Mutat
, vol.2
, pp. 159
-
-
Vulliamy, T.1
Beutler, E.2
Luzzatto, L.3
-
419
-
-
0028339178
-
Molecular study of eight Japanese cases of glucose-6-phosphate dehydrogenase deficiency by nonradioisotopic single-strand conformation polymorphism analysis
-
Hirono A, Miwa S, Fujii H, Ishida F, Yamada K, Kubota K: Molecular study of eight Japanese cases of glucose-6-phosphate dehydrogenase deficiency by nonradioisotopic single-strand conformation polymorphism analysis. Blood 83:3363, 1994
-
(1994)
Blood
, vol.83
, pp. 3363
-
-
Hirono, A.1
Miwa, S.2
Fujii, H.3
Ishida, F.4
Yamada, K.5
Kubota, K.6
-
420
-
-
0025871176
-
Mutation analysis of G6PD variants in Costa Rica
-
Beutler E, Kuhl W, Śaenz GF, Rodriguez W: Mutation analysis of G6PD variants in Costa Rica. Hum Genet 87:462, 1991
-
(1991)
Hum Genet
, vol.87
, pp. 462
-
-
Beutler, E.1
Kuhl, W.2
Śaenz, G.F.3
Rodriguez, W.4
-
421
-
-
0024493798
-
Two point mutations are responsible for G6PD polymorphism in Sardinia
-
De Vita G, Alcalay M, Sampietro M, Cappellini MD, Fiorelli G, Toniolo D: Two point mutations are responsible for G6PD polymorphism in Sardinia. Am J Hum Genet 44:233, 1989
-
(1989)
Am J Hum Genet
, vol.44
, pp. 233
-
-
De Vita, G.1
Alcalay, M.2
Sampietro, M.3
Cappellini, M.D.4
Fiorelli, G.5
Toniolo, D.6
-
422
-
-
0026603606
-
Molecular heterogeneity underlying the G6PD Mediterranean phenotype
-
Corcoran CM, Calabr̀o V, Tamagnini G, Town M, Haidar B, Vulliamy TJ, Mason PJ, Luzzatto L: Molecular heterogeneity underlying the G6PD Mediterranean phenotype. Hum Genet 88:688, 1992
-
(1992)
Hum Genet
, vol.88
, pp. 688
-
-
Corcoran, C.M.1
Calabr̀o, V.2
Tamagnini, G.3
Town, M.4
Haidar, B.5
Vulliamy, T.J.6
Mason, P.J.7
Luzzatto, L.8
-
423
-
-
0026766491
-
New glucose-6-phosphate dehydrogenase mutations from various ethnic groups
-
Beutler E, Westwood B, Prchal J, Vaca G, Bartsocas CS, Baronciani L: New glucose-6-phosphate dehydrogenase mutations from various ethnic groups. Blood 80:255, 1992
-
(1992)
Blood
, vol.80
, pp. 255
-
-
Beutler, E.1
Westwood, B.2
Prchal, J.3
Vaca, G.4
Bartsocas, C.S.5
Baronciani, L.6
-
424
-
-
0026357097
-
Definition of the mutations of G6HD Wayne, G6PD Viangchan, G6PD Jammu and G6PD "LeJeune"
-
Beutler E, Prchal JT, Westwood B, Kuhl W: Definition of the mutations of G6HD Wayne, G6PD Viangchan, G6PD Jammu and G6PD "LeJeune". Acta Haematol 86:179, 1991
-
(1991)
Acta Haematol
, vol.86
, pp. 179
-
-
Beutler, E.1
Prchal, J.T.2
Westwood, B.3
Kuhl, W.4
-
425
-
-
0003233994
-
Point mutations in two G6PD variants previously described in Italy
-
abstr
-
Fiorelli G, Anghinelli L, Carandina G, Toniolo D, Sempietro M, Cappellini MD, Pareti FI: Point mutations in two G6PD variants previously described in Italy. Blood 76:7a, 1990 (suppl, abstr)
-
(1990)
Blood
, vol.76
, Issue.SUPPL.
-
-
Fiorelli, G.1
Anghinelli, L.2
Carandina, G.3
Toniolo, D.4
Sempietro, M.5
Cappellini, M.D.6
Pareti, F.I.7
-
426
-
-
0025055118
-
Common glucose-6-phosphate dehydrogenase (G6PD) variants from the Italian population: Biochemical and molecular characterization
-
Viglietto G, Montanaro V, Calabro V, Vallone D, D'Urso M, Persico MG, Battistuzzi G: Common glucose-6-phosphate dehydrogenase (G6PD) variants from the Italian population: Biochemical and molecular characterization. Ann Hum Genet 54:1, 1990
-
(1990)
Ann Hum Genet
, vol.54
, pp. 1
-
-
Viglietto, G.1
Montanaro, V.2
Calabro, V.3
Vallone, D.4
D'Urso, M.5
Persico, M.G.6
Battistuzzi, G.7
-
427
-
-
0026879380
-
G6PD Kalyan and G6PD Kerala; two deficient variants in India caused by the same 317 Glu→Lys mutation
-
Ahluwalia A, Corcoran CM, Vulliamy TJ, Ishwad CS, Naidu JM, Argusti A, Stevens DJ, Mason PJ, Luzzatto L: G6PD Kalyan and G6PD Kerala; two deficient variants in India caused by the same 317 Glu→Lys mutation. Hum Mol Genet 1:209, 1992
-
(1992)
Hum Mol Genet
, vol.1
, pp. 209
-
-
Ahluwalia, A.1
Corcoran, C.M.2
Vulliamy, T.J.3
Ishwad, C.S.4
Naidu, J.M.5
Argusti, A.6
Stevens, D.J.7
Mason, P.J.8
Luzzatto, L.9
-
428
-
-
0027331492
-
G6PD Nara: A new class 1 glucose-6-phosphate dehydrogenase variant with an eight amino acid deletion
-
Hirono A, Fujii H, Shima M, Miwa S: G6PD Nara: A new class 1 glucose-6-phosphate dehydrogenase variant with an eight amino acid deletion. Blood 82:3250, 1993
-
(1993)
Blood
, vol.82
, pp. 3250
-
-
Hirono, A.1
Fujii, H.2
Shima, M.3
Miwa, S.4
-
430
-
-
0026541412
-
GPD and marked instability
-
GPD and marked instability. Br J Haematol 80:111, 1992
-
(1992)
Br J Haematol
, vol.80
, pp. 111
-
-
Filosa, S.1
Calabr̀o, V.2
Vallone, D.3
Poggi, V.4
Mason, P.5
Pagnini, D.6
Alfinito, F.7
Rotoli, B.8
Martini, G.9
Luzzatto, L.10
Battistuzzi, G.11
-
431
-
-
0026513093
-
Molecular abnormality of a Japanese glucose-6-phosphate dehydrogenase variant (G6PD Tokyo) associated with hereditary non-spherocytic hemolytic anemia
-
Hirono A, Fujii H, Hirono K, Kanno H, Miwa S: Molecular abnormality of a Japanese glucose-6-phosphate dehydrogenase variant (G6PD Tokyo) associated with hereditary non-spherocytic hemolytic anemia. Hum Genet 88:347, 1992
-
(1992)
Hum Genet
, vol.88
, pp. 347
-
-
Hirono, A.1
Fujii, H.2
Hirono, K.3
Kanno, H.4
Miwa, S.5
-
432
-
-
0028218784
-
Molecular abnormality of a unique Japanese glucose-6-phosphate dehydrogenase variant (G6PD Kobe) with a greatly increased affinity for galactose-6-phosphate
-
Hirono A, Nakayama S, Fujii H, Miwa S: Molecular abnormality of a unique Japanese glucose-6-phosphate dehydrogenase variant (G6PD Kobe) with a greatly increased affinity for galactose-6-phosphate. Am J Hematol 45:185, 1994
-
(1994)
Am J Hematol
, vol.45
, pp. 185
-
-
Hirono, A.1
Nakayama, S.2
Fujii, H.3
Miwa, S.4
-
434
-
-
0025831075
-
Two commonly occurring nucleotide base substitutions in Chinese G6PD variants
-
Chiu DTY, Zuo L, Chen E, Chao L, Louie E, Lubin B, Liu TZ, Du C-S: Two commonly occurring nucleotide base substitutions in Chinese G6PD variants. Biochem Biophys Res Commun 180:988, 1991
-
(1991)
Biochem Biophys Res Commun
, vol.180
, pp. 988
-
-
Chiu, D.T.Y.1
Zuo, L.2
Chen, E.3
Chao, L.4
Louie, E.5
Lubin, B.6
Liu, T.Z.7
Du, C.-S.8
-
435
-
-
0025605094
-
G6PD Canton a common deficient variant in South East Asia caused by a 459 Arg→Leu mutation
-
Stevens DJ, Wanachiwanawin W, Mason PJ, Vulliamy TJ, Luzzatto L: G6PD Canton a common deficient variant in South East Asia caused by a 459 Arg→Leu mutation. Nucleic Acids Res 18:7190, 1990
-
(1990)
Nucleic Acids Res
, vol.18
, pp. 7190
-
-
Stevens, D.J.1
Wanachiwanawin, W.2
Mason, P.J.3
Vulliamy, T.J.4
Luzzatto, L.5
-
436
-
-
0025376470
-
202A/376G: Evidence for a single origin of the common G6PD A- mutation
-
202A/376G: Evidence for a single origin of the common G6PD A- mutation. Hum Genet 85:9, 1990
-
(1990)
Hum Genet
, vol.85
, pp. 9
-
-
Beutler, E.1
Kuhl, W.2
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