-
2
-
-
0040982409
-
Studies on hemoglobin E I. The clinical, hematologic, and genetic characteristics of the hemoglobin E syndromes
-
Chemoff AI, Minnich V, Na-Nakorn S, Tuchinda S, Kashemsant C, Chrenoff RR: Studies on hemoglobin E I. The clinical, hematologic, and genetic characteristics of the hemoglobin E syndromes. J Lab Clin Med 47:455, 1956
-
(1956)
J Lab Clin Med
, vol.47
, pp. 455
-
-
Chemoff, A.I.1
Minnich, V.2
Na-Nakorn, S.3
Tuchinda, S.4
Kashemsant, C.5
Chrenoff, R.R.6
-
3
-
-
0020376275
-
Abnormal RNA processing due to the exon mutation of betaE-globin gene
-
Orkin SH Jr, Kazazian HH Jr, Antonarakis SE, Ostrer H, Goff SC, Sexton JP: Abnormal RNA processing due to the exon mutation of betaE-globin gene. Nature 300:768, 1982
-
(1982)
Nature
, vol.300
, pp. 768
-
-
Orkin Jr., S.H.1
Kazazian Jr., H.H.2
Antonarakis, S.E.3
Ostrer, H.4
Goff, S.C.5
Sexton, J.P.6
-
4
-
-
0019316743
-
Defective synthesis of HbE is due to reduced levels of βE mRNA
-
Traeger J, Wood WG, Clegg JB, Weatherall DJ, Wasi P: Defective synthesis of HbE is due to reduced levels of βE mRNA. Nature 288:497, 1980
-
(1980)
Nature
, vol.288
, pp. 497
-
-
Traeger, J.1
Wood, W.G.2
Clegg, J.B.3
Weatherall, D.J.4
Wasi, P.5
-
5
-
-
0016736939
-
Hemoglobin E, an oxidatively unstable mutation
-
Frischer H, Bowman J: Hemoglobin E, an oxidatively unstable mutation. J Lab Clin Med 85:531, 1975
-
(1975)
J Lab Clin Med
, vol.85
, pp. 531
-
-
Frischer, H.1
Bowman, J.2
-
6
-
-
0023491626
-
Variable severity of Southeast Asian β-thalassaemia/Hb e disease
-
Fucharoen S, Winichagoon P, Pootrakul P, Piankijagum A, Wasi P: Variable severity of Southeast Asian β-thalassaemia/Hb E disease. Birth Defects: Original Article Series 53:241, 1988
-
(1988)
Birth Defects: Original Article Series
, vol.53
, pp. 241
-
-
Fucharoen, S.1
Winichagoon, P.2
Pootrakul, P.3
Piankijagum, A.4
Wasi, P.5
-
7
-
-
0027408741
-
Severity differences in β-thalassaemia/haemoglobin E syndromes: Implication of genetic factors
-
Winichagoon P, Thonglairoam V, Fucharoen S, Wilairat P, Fukumaki Y, Wasi P: Severity differences in β-thalassaemia/haemoglobin E syndromes: Implication of genetic factors. Br J Haematol 83:633, 1993
-
(1993)
Br J Haematol
, vol.83
, pp. 633
-
-
Winichagoon, P.1
Thonglairoam, V.2
Fucharoen, S.3
Wilairat, P.4
Fukumaki, Y.5
Wasi, P.6
-
8
-
-
0016201961
-
Hereditary hemolytic anaemia with human erythrocyte pyrimidine 5′-nucleotidase deficiency
-
Valentine WN, Fink K, Paglia DE, Harris SR, Adams WS: Hereditary hemolytic anaemia with human erythrocyte pyrimidine 5′-nucleotidase deficiency. J Clin Invest 54:866, 1974
-
(1974)
J Clin Invest
, vol.54
, pp. 866
-
-
Valentine, W.N.1
Fink, K.2
Paglia, D.E.3
Harris, S.R.4
Adams, W.S.5
-
9
-
-
0018954552
-
Hemolytic anemia due to pyrimidine-5′-nucleotidase deficiency: Report of eight cases in six families
-
Beutler E, Baranko PV, Feagler J, Matsumoto F, Miro-Quesdada M, Selby G, Singh P: Hemolytic anemia due to pyrimidine-5′-nucleotidase deficiency: Report of eight cases in six families. Blood 56:251, 1980
-
(1980)
Blood
, vol.56
, pp. 251
-
-
Beutler, E.1
Baranko, P.V.2
Feagler, J.3
Matsumoto, F.4
Miro-Quesdada, M.5
Selby, G.6
Singh, P.7
-
10
-
-
0020383946
-
Hemolytic anemia in hereditary pyrimidine 5′-nucleotidase deficiency: Nucleotide inhibition of G6PD and the pentose phosphate shunt
-
Tomoda A, Noble NA, Lachant NA, Tanaka KR: Hemolytic anemia in hereditary pyrimidine 5′-nucleotidase deficiency: Nucleotide inhibition of G6PD and the pentose phosphate shunt. Blood 60:1212, 1982
-
(1982)
Blood
, vol.60
, pp. 1212
-
-
Tomoda, A.1
Noble, N.A.2
Lachant, N.A.3
Tanaka, K.R.4
-
11
-
-
0024424193
-
Pyrimidine 5′-nucleotidase acquired deficiency in β-thalassaemia: Involvement of enzyme-SH groups in the inactivation process
-
David O, Volta MG, Piga A, Ramenghi U, Bosia A, Pescarmona GP: Pyrimidine 5′-nucleotidase acquired deficiency in β-thalassaemia: Involvement of enzyme-SH groups in the inactivation process. Acta Haematol 82:69, 1989
-
(1989)
Acta Haematol
, vol.82
, pp. 69
-
-
David, O.1
Volta, M.G.2
Piga, A.3
Ramenghi, U.4
Bosia, A.5
Pescarmona, G.P.6
-
13
-
-
4243313142
-
Methods of determining hemoglobin instability (unstable hemoglobins)
-
Huisman THJ (ed): London, UK, Churchill Livingstone
-
Carrell RW: Methods of determining hemoglobin instability (unstable hemoglobins), in Huisman THJ (ed): The Hemoglobinopathies. London, UK, Churchill Livingstone, 1986, p 109
-
(1986)
The Hemoglobinopathies
, pp. 109
-
-
Carrell, R.W.1
-
14
-
-
0002804385
-
Gene analysis
-
Weatherall DJ (ed): London, UK, Churchill Livingstone
-
Old JM, Higgs DR: Gene analysis, in Weatherall DJ (ed): The Thalassaemias. London, UK, Churchill Livingstone, 1983, p 74
-
(1983)
The Thalassaemias
, pp. 74
-
-
Old, J.M.1
Higgs, D.R.2
-
15
-
-
0027202405
-
β-Thalassaemia unlinked to the β-globin gene in an English family
-
Thein SL, Wood WG, Wickramasinghe SN, Galvin MC: β-Thalassaemia unlinked to the β-globin gene in an English family. Blood 82:961, 1993
-
(1993)
Blood
, vol.82
, pp. 961
-
-
Thein, S.L.1
Wood, W.G.2
Wickramasinghe, S.N.3
Galvin, M.C.4
-
16
-
-
0025993003
-
A simple and rapid method of direct sequencing using Dynabeads
-
Thein SL, Hinton J: A simple and rapid method of direct sequencing using Dynabeads. Br J Haematol 79:113, 1991
-
(1991)
Br J Haematol
, vol.79
, pp. 113
-
-
Thein, S.L.1
Hinton, J.2
-
17
-
-
0027938162
-
Hpa I, Hind III, and BamHI polymorphisms 3′ of the human β-globin gene can be detected by a single polymerase chain reaction
-
Fullerton SM, Clegg JB: Hpa I, Hind III, and BamHI polymorphisms 3′ of the human β-globin gene can be detected by a single polymerase chain reaction. Am J Hematol 47:256, 1994
-
(1994)
Am J Hematol
, vol.47
, pp. 256
-
-
Fullerton, S.M.1
Clegg, J.B.2
-
18
-
-
0024376665
-
Polymerase chain reaction amplification applied to the determination of β-like globin cluster haplotypes
-
Sutton M, Bouhassira E, Nagel R: Polymerase chain reaction amplification applied to the determination of β-like globin cluster haplotypes. Am J Hematol 32:66, 1989
-
(1989)
Am J Hematol
, vol.32
, pp. 66
-
-
Sutton, M.1
Bouhassira, E.2
Nagel, R.3
-
19
-
-
0021472454
-
The molecular basis of alpha-thalassaemia in Thailand
-
Winichagoon P, Higgs DR, Goodbourn SEY, Clegg JB, Weatherall DJ, Wasi P: The molecular basis of alpha-thalassaemia in Thailand. EMBO J 3:1813, 1984
-
(1984)
EMBO J
, vol.3
, pp. 1813
-
-
Winichagoon, P.1
Higgs, D.R.2
Sey, G.3
Clegg, J.B.4
Weatherall, D.J.5
Wasi, P.6
-
20
-
-
0003946353
-
-
London, UK, Churchill Livingstone
-
Beutler E: Red Cell Metabolism. London, UK, Churchill Livingstone, 1986
-
(1986)
Red Cell Metabolism
-
-
Beutler, E.1
-
21
-
-
0001964301
-
Analysis of purines and pyrimidines in blood, urine and other physiological fluids
-
Hommes FA (ed): New York, NY, Wiley-Liss
-
Simmonds HA, Duley JA, Davies PM: Analysis of purines and pyrimidines in blood, urine and other physiological fluids, in Hommes FA (ed): Techniques in Diagnostic Human Biochemical Genetics: A Laboratory Manual. New York, NY, Wiley-Liss, 1991, p 397
-
(1991)
Techniques in Diagnostic Human Biochemical Genetics: A Laboratory Manual
, pp. 397
-
-
Simmonds, H.A.1
Duley, J.A.2
Davies, P.M.3
-
22
-
-
0017185162
-
The removal of leukocytes and platelets from whole blood
-
Beutler E, West C, Blume K-G: The removal of leukocytes and platelets from whole blood. J Lab Clin Med 88:328, 1976
-
(1976)
J Lab Clin Med
, vol.88
, pp. 328
-
-
Beutler, E.1
West, C.2
Blume, K.-G.3
-
23
-
-
0003026329
-
Hemoglobin Synthesis
-
Weatherall DJ (ed): London, UK, Churchill Livingstone
-
Clegg JB: Hemoglobin Synthesis, in Weatherall DJ (ed): The Thalassaemias. London, UK, Churchill Livingstone, 1983, p 54
-
(1983)
The Thalassaemias
, pp. 54
-
-
Clegg, J.B.1
-
24
-
-
50549175610
-
The preparation and chemical characteristics of hemoglobin-free ghosts of human erythrocytes
-
Dodge JT, Mitchell C, Hanahan DJ: The preparation and chemical characteristics of hemoglobin-free ghosts of human erythrocytes. Arch Biochem Biophys 100:119, 1963
-
(1963)
Arch Biochem Biophys
, vol.100
, pp. 119
-
-
Dodge, J.T.1
Mitchell, C.2
Hanahan, D.J.3
-
25
-
-
0014486517
-
The pattern of disordered haemoglobin synthesis in homozygous and heterozygous β-thalassaetnia
-
Weatherall DJ, Clegg JB, Na-Nakorn S, Wasi P: The pattern of disordered haemoglobin synthesis in homozygous and heterozygous β-thalassaetnia. Br J Haematol 16:251, 1969
-
(1969)
Br J Haematol
, vol.16
, pp. 251
-
-
Weatherall, D.J.1
Clegg, J.B.2
Na-Nakorn, S.3
Wasi, P.4
-
26
-
-
8944258107
-
A novel silent post-translational mechanism converts methionine to aspartate in hemoglobin Bristol [β67(E11) Val → Met → Asp]
-
Rees DC, Rochette J, Schofield C, Green B, Morris M, Parker NE, Sasaki H, Tanaka A, Ohba Y, Clegg JB: A novel silent post-translational mechanism converts methionine to aspartate in hemoglobin Bristol [β67(E11) Val → Met → Asp]. Blood 88:341, 1996
-
(1996)
Blood
, vol.88
, pp. 341
-
-
Rees, D.C.1
Rochette, J.2
Schofield, C.3
Green, B.4
Morris, M.5
Parker, N.E.6
Sasaki, H.7
Tanaka, A.8
Ohba, Y.9
Clegg, J.B.10
-
27
-
-
0015514250
-
Characterization of Heinz bodies in unstable haemoglobin haemolytic anaemia
-
Winterbourn CC, Carrell RW: Characterization of Heinz bodies in unstable haemoglobin haemolytic anaemia. Nature 240:150, 1972
-
(1972)
Nature
, vol.240
, pp. 150
-
-
Winterbourn, C.C.1
Carrell, R.W.2
-
28
-
-
0015577143
-
Nonspherocytic haemolytic anaemia with increased red cell adenine nucleotides, glutathione and basophilic stippling and ribosephosphate pyrophosphokinase (RPK) deficiency: Studies on two new kindreds
-
Valentine WN, Bennett JM, Krivit W, Konrad PN, Lowman JT, Paglia DE, Wakem CJ: Nonspherocytic haemolytic anaemia with increased red cell adenine nucleotides, glutathione and basophilic stippling and ribosephosphate pyrophosphokinase (RPK) deficiency: Studies on two new kindreds. Br J Haematol 24:157, 1973
-
(1973)
Br J Haematol
, vol.24
, pp. 157
-
-
Valentine, W.N.1
Bennett, J.M.2
Krivit, W.3
Konrad, P.N.4
Lowman, J.T.5
Paglia, D.E.6
Wakem, C.J.7
-
29
-
-
0003739602
-
-
Philadelphia, PA, Saunders
-
Bunn HF, Forget BG: Hemoglobin: Molecular, Genetic and Clinical Aspects. Philadelphia, PA, Saunders, 1986
-
(1986)
Hemoglobin: Molecular, Genetic and Clinical Aspects
-
-
Bunn, H.F.1
Forget, B.G.2
-
30
-
-
0028849492
-
Thalassaemic erythrocytes: Cellular suicide arising from iron and glutathione-dependent oxidation reactions?
-
Scott MD, Eaton JW: Thalassaemic erythrocytes: Cellular suicide arising from iron and glutathione-dependent oxidation reactions? Br J Haematol 91:811, 1995
-
(1995)
Br J Haematol
, vol.91
, pp. 811
-
-
Scott, M.D.1
Eaton, J.W.2
-
31
-
-
0003557633
-
-
Philadelphia, PA, Saunders
-
Bunn HF, Forget BG, Ranney HM: Human Hemoglobins. Philadelphia, PA, Saunders, 1977
-
(1977)
Human Hemoglobins
-
-
Bunn, H.F.1
Forget, B.G.2
Ranney, H.M.3
-
32
-
-
0023640946
-
Case report: Dapsone-associated Heinz body hemolytic anemia in a Cambodian woman with hemoglobin E trait
-
Lachant NA, Tanaka KR: Case report: Dapsone-associated Heinz body hemolytic anemia in a Cambodian woman with hemoglobin E trait. Am J Med Sci 294:364, 1987
-
(1987)
Am J Med Sci
, vol.294
, pp. 364
-
-
Lachant, N.A.1
Tanaka, K.R.2
-
33
-
-
0026632395
-
Hemoglobin-E in the presence of oxidative substances from fava bean may be protective against Plasmodium falciparum malaria
-
Kitayaporn D, Nelson KE, Charoenlarp P, Pholpothi T: Hemoglobin-E in the presence of oxidative substances from fava bean may be protective against Plasmodium falciparum malaria. Trans R Soc Trop Med Hyg 86:240, 1992
-
(1992)
Trans R Soc Trop Med Hyg
, vol.86
, pp. 240
-
-
Kitayaporn, D.1
Nelson, K.E.2
Charoenlarp, P.3
Pholpothi, T.4
-
34
-
-
3543135027
-
Triple erythropoietic anomaly: Porphyria, glucose-6-phosphate dehydrogenase deficiency and heterozygous state of haemoglobin E
-
Chatterji AK, Ghosh SK, Chatterjea JB: Triple erythropoietic anomaly: Porphyria, glucose-6-phosphate dehydrogenase deficiency and heterozygous state of haemoglobin E. J Assoc Physicians India 11:941, 1963
-
(1963)
J Assoc Physicians India
, vol.11
, pp. 941
-
-
Chatterji, A.K.1
Ghosh, S.K.2
Chatterjea, J.B.3
-
35
-
-
0019239930
-
HbE-β-thalassaemia associated with G6PD deficiency
-
Carpentieri U, Haggard ME, Schneider RG, Hightower BJ: HbE-β-thalassaemia associated with G6PD deficiency. Southern Med J 73:518, 1980
-
(1980)
Southern Med J
, vol.73
, pp. 518
-
-
Carpentieri, U.1
Haggard, M.E.2
Schneider, R.G.3
Hightower, B.J.4
-
36
-
-
0026846795
-
Prevalence of malaria in Ao Nagas and its association with G6PD and Hb E
-
Kar S, Seth S, Seth PK: Prevalence of malaria in Ao Nagas and its association with G6PD and Hb E. Hum Biol 64:187, 1992
-
(1992)
Hum Biol
, vol.64
, pp. 187
-
-
Kar, S.1
Seth, S.2
Seth, P.K.3
-
37
-
-
0024727726
-
Homozygous haemoglobin E in association with hereditary ovalocytosis
-
George E, Kudva MV: Homozygous haemoglobin E in association with hereditary ovalocytosis. Med J Malaysia 44:255, 1989
-
(1989)
Med J Malaysia
, vol.44
, pp. 255
-
-
George, E.1
Kudva, M.V.2
-
38
-
-
0014831607
-
Hereditary elliptocytosis (the first report in Thailand) in association with erythrocyte glucose-6-phosphate dehydrogenase deficiency and hemoglobin E
-
Panich V, Na-Nakorn S, Wasi P: Hereditary elliptocytosis (the first report in Thailand) in association with erythrocyte glucose-6-phosphate dehydrogenase deficiency and hemoglobin E. J Med Assoc Thailand 53:593, 1970
-
(1970)
J Med Assoc Thailand
, vol.53
, pp. 593
-
-
Panich, V.1
Na-Nakorn, S.2
Wasi, P.3
-
39
-
-
0021360612
-
Pyrimidine 5′ nucleotidase and several other red cell enzyme activities in β-thalassaemia trait
-
Corrons JLV, Pujades MA, Aguilar i Bascompte JL, Jou JM, Rozman C, Ester A: Pyrimidine 5′ nucleotidase and several other red cell enzyme activities in β-thalassaemia trait. Br J Haematol 56:483, 1984
-
(1984)
Br J Haematol
, vol.56
, pp. 483
-
-
Corrons, J.L.V.1
Pujades, M.A.2
Aguilar I Bascompte, J.L.3
Jou, J.M.4
Rozman, C.5
Ester, A.6
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