-
1
-
-
0001585429
-
Glucose-6-phosphate dehydrogenase deficiency
-
Scriver CR, Beaudet AL, Sly WS, Valle D, editors. London: McGraw-Hill
-
Luzzatto L, Metha A. Glucose-6-phosphate dehydrogenase deficiency. In: Scriver CR, Beaudet AL, Sly WS, Valle D, editors. The metabolic basis of inherited disease. London: McGraw-Hill, 1988:2237.
-
(1988)
The Metabolic Basis of Inherited Disease
, pp. 2237
-
-
Luzzatto, L.1
Metha, A.2
-
2
-
-
0000702174
-
Glucose-6-phosphate dehydrogenase deficiency in Saudi Arabia, a survey
-
Gelpi AP. Glucose-6-phosphate dehydrogenase deficiency in Saudi Arabia, a survey. Blood 1965; 25:486-93.
-
(1965)
Blood
, vol.25
, pp. 486-493
-
-
Gelpi, A.P.1
-
3
-
-
0022630805
-
Frequency of G6PD, PK and hexokinase deficiency in the Saudi population
-
El-Hazmi MAF, Al-Swailem AR, Al-Faleh FZ, Warsy AS. Frequency of G6PD, PK and hexokinase deficiency in the Saudi population. Hum Hered 1986; 36:45-9.
-
(1986)
Hum. Hered
, vol.36
, pp. 45-49
-
-
El-Hazmi, M.A.F.1
Al-Swailem, A.R.2
Al-Faleh, F.Z.3
Warsy, A.S.4
-
4
-
-
0027940492
-
G6PD deficiency
-
Beutler E. G6PD deficiency. Blood 1994; 84:3613-36.
-
(1994)
Blood
, vol.84
, pp. 3613-3636
-
-
Beutler, E.1
-
5
-
-
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 1979; 43:263-74.
-
(1979)
Br. J. Haematol
, vol.43
, pp. 263-274
-
-
Gibbs, W.N.1
Gray, R.2
Lowry, M.3
-
6
-
-
0023255855
-
Favism; impairment of proteolytic system in RBC
-
Morelli A, Grasso M, Meloni T, Forteleoni G, Zocchi E, De Flora A. Favism; impairment of proteolytic system in RBC. Blood 1987; 69:1753-8.
-
(1987)
Blood
, vol.69
, pp. 1753-1758
-
-
Morelli, A.1
Grasso, M.2
Meloni, T.3
Forteleoni, G.4
Zocchi, E.5
De Flora, A.6
-
7
-
-
0030497637
-
Common G6PD variant from Saudi population and its prevalence
-
Al-Ali AK. Common G6PD variant from Saudi population and its prevalence. Ann Saudi Med 1996; 4:654-6.
-
(1996)
Ann. Saudi Med
, vol.4
, pp. 654-656
-
-
Al-Ali, A.K.1
-
8
-
-
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, et al. Origin and spread of the glucose-6-phosphate dehydrogenase variant (G6PD-Mediterranean) in the Middle East. Am J Hum Genet 1990; 4:1013-9.
-
(1990)
Am. J. Hum. Genet
, vol.4
, pp. 1013-1019
-
-
Kurdi-Haidar, B.1
Mason, P.J.2
Berrebi, A.3
Ankra-Badu, G.4
Al-Ali, A.5
Oppenheim, A.6
-
10
-
-
13844295080
-
-
Ser. 366
-
Betke K, Brewer GJ, Kirkman HN, Luzzatto L, Motulsky AG, Ramot B, et al. WHO Tech Rep 1967; Ser. 366.
-
(1967)
WHO Tech. Rep
-
-
Betke, K.1
Brewer, G.J.2
Kirkman, H.N.3
Luzzatto, L.4
Motulsky, A.G.5
Ramot, B.6
-
12
-
-
0025165882
-
Identification of a single base change in new human mutant glucose-6-phosphate dehydrogenase gene by PCR amplification of the entire coding region from genomic DNA
-
Poggi V, Town M, Foulkes NS, Luzzatto L. Identification of a single base change in new human mutant glucose-6-phosphate dehydrogenase gene by PCR amplification of the entire coding region from genomic DNA. Biochem J 1990; 271:157-60.
-
(1990)
Biochem. J
, vol.271
, pp. 157-160
-
-
Poggi, V.1
Town, M.2
Foulkes, N.S.3
Luzzatto, L.4
-
13
-
-
0026580948
-
The molecular basis of glucose-6-phosphate dehydrogenase deficiency
-
Vulliamy TJ, Mason P, Luzzatto L. The molecular basis of glucose-6-phosphate dehydrogenase deficiency. Trends Genet 1992; 8:138-43.
-
(1992)
Trends Genet
, vol.8
, pp. 138-143
-
-
Vulliamy, T.J.1
Mason, P.2
Luzzatto, L.3
-
14
-
-
0027537149
-
G6PD Aures: a new mutation (14 Ile to thr) causing mild G6PD deficiency is associated with favism
-
Nafa K, Reghis A, Osmani N, Benabadji M, Kaplan JC, Vulliamy TJ, et al. G6PD Aures: a new mutation (14 Ile to thr) causing mild G6PD deficiency is associated with favism. Hum Mol Genet 1993; 2:81-2.
-
(1993)
Hum. Mol. Genet
, vol.2
, pp. 81-82
-
-
Nafa, K.1
Reghis, A.2
Osmani, N.3
Benabadji, M.4
Kaplan, J.C.5
Vulliamy, T.J.6
-
15
-
-
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, et al. 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 1988; 85:5171-5.
-
(1988)
Proc. Natl. Acad. Sci. USA
, vol.85
, pp. 5171-5175
-
-
Vulliamy, T.J.1
D'Urso, M.2
Battistuzzi, G.3
Estrada, M.4
Foulkes, N.S.5
Martini, G.6
-
16
-
-
0024455091
-
Molecular heterogeneity of glucose-6-phosphate dehydrogenase A
-
Beutler E, Kuhl W, Vives-Corrons JL, Prchal JT. Molecular heterogeneity of glucose-6-phosphate dehydrogenase A. Blood 1989; 74:2550-5.
-
(1989)
Blood
, vol.74
, pp. 2550-2555
-
-
Beutler, E.1
Kuhl, W.2
Vives-Corrons, J.L.3
Prchal, J.T.4
-
17
-
-
0029924661
-
Molecular characterization of G6PD deficiency in Oman
-
Daar S, Vulliamy TJ, Kaedaj J, Mason PJ, Luzzatto L. Molecular characterization of G6PD deficiency in Oman. Hum Hered 1996; 46:172-6.
-
(1996)
Hum. Hered
, vol.46
, pp. 172-176
-
-
Daar, S.1
Vulliamy, T.J.2
Kaedaj, J.3
Mason, P.J.4
Luzzatto, L.5
-
19
-
-
13344284636
-
Molecular characterization of erythrocyte glucose-6-phosphate dehydrogenase deficiency in Al-Ain District, United Arab Emirates
-
Bayoumi RA, Nur-E-Kamal MS, Tadayyon M, Mohamed KK, Mahboob BH, Qureshi MM, et al. Molecular characterization of erythrocyte glucose-6-phosphate dehydrogenase deficiency in Al-Ain District, United Arab Emirates. Hum Hered 1996; 46:136-41.
-
(1996)
Hum. Hered
, vol.46
, pp. 136-141
-
-
Bayoumi, R.A.1
Nur-E-Kamal, M.S.2
Tadayyon, M.3
Mohamed, K.K.4
Mahboob, B.H.5
Qureshi, M.M.6
|