-
1
-
-
0001585429
-
Glucose 6-phosphate dehydrogenase deficiency
-
Scriver CR, Beaudet AL, Sly WS, Valle D, eds. New York: McGraw-Hill
-
Luzzatto L, Mehta A, Vulliamy T. Glucose 6-phosphate dehydrogenase deficiency. In: Scriver CR, Beaudet AL, Sly WS, Valle D, eds. The Metabolic and Molecular Bases of Inherited Disease, 8th ed. New York: McGraw-Hill; 2001:4517-4553.
-
(2001)
The Metabolic and Molecular Bases of Inherited Disease, 8th Ed.
, pp. 4517-4553
-
-
Luzzatto, L.1
Mehta, A.2
Vulliamy, T.3
-
2
-
-
0015170235
-
Human glucose-6-phosphate dehydrogenase variants
-
Yoshida A, Beutler E, Motulsky AG. Human glucose-6-phosphate dehydrogenase variants. Bull WHO. 1971;45:243-253.
-
(1971)
Bull WHO
, vol.45
, pp. 243-253
-
-
Yoshida, A.1
Beutler, E.2
Motulsky, A.G.3
-
4
-
-
0017185162
-
The removal of leukocytes and platelets from whole blood
-
Beutler E, West C, Blume KG. The removal of leukocytes and platelets from whole blood. J Lab Clin Med. 1976;88:328-333.
-
(1976)
J Lab Clin Med
, vol.88
, pp. 328-333
-
-
Beutler, E.1
West, C.2
Blume, K.G.3
-
6
-
-
0028339178
-
Molecular study of eight Japanese cases of glucose-6-phosphate dehydrogenase deficiency by non-radioisotopic 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 non-radioisotopic single-strand conformation polymorphism analysis. Blood.1994;83:3363-3368.
-
(1994)
Blood
, vol.83
, pp. 3363-3368
-
-
Hirono, A.1
Miwa, S.2
Fujii, H.3
Ishida, F.4
Yamada, K.5
Kubota, K.6
-
7
-
-
0015183031
-
Glutathion, Glutathionperoxydase, Glutathionreduktase, Glucose-6-Phosphatdehydrogenase, Lactatdehydrogenase und Katalase in Erythrocyten von Neugeborenen, Säuglingen und Kindern und ihre Beziehung zur Heinzkörperbildung
-
Butenandt O. Glutathion, Glutathionperoxydase, Glutathionreduktase, Glucose-6-Phosphatdehydrogenase, Lactatdehydrogenase und Katalase in Erythrocyten von Neugeborenen, Säuglingen und Kindern und ihre Beziehung zur Heinzkörperbildung. Z Kinderheilk. 1971;111:149-161.
-
(1971)
Z Kinderheilk
, vol.111
, pp. 149-161
-
-
Butenandt, O.1
-
8
-
-
0015460987
-
Enzymatic activities and glutathione content of erythrocytes in the newborn: Comparison with red cells of older normal subjects and those with comparable reticulocytosis
-
Konrad PN, Valentine WN, Paglia DE. Enzymatic activities and glutathione content of erythrocytes in the newborn: comparison with red cells of older normal subjects and those with comparable reticulocytosis. Acta Haemat. 1972;48:193-201.
-
(1972)
Acta Haemat
, vol.48
, pp. 193-201
-
-
Konrad, P.N.1
Valentine, W.N.2
Paglia, D.E.3
-
9
-
-
0029842792
-
Somatic-cell selection is a major determinant of the blood-cell phenotype in heterozygotes for glucose-6-phosphate dehydrogenase mutations causing severe enzyme deficiency
-
Filosa S, Giacometti N, Wangwei C, et al. Somatic-cell selection is a major determinant of the blood-cell phenotype in heterozygotes for glucose-6-phosphate dehydrogenase mutations causing severe enzyme deficiency. Am J Hum Genet. 1996;59:887-895.
-
(1996)
Am J Hum Genet
, vol.59
, pp. 887-895
-
-
Filosa, S.1
Giacometti, N.2
Wangwei, C.3
-
10
-
-
85037309353
-
Heterozygotes for G6PD deficiency with class 1 variants may not be diagnosed solely by red cell enzyme assay
-
Hirono A, Fujii H, Miwa S. Heterozygotes for G6PD deficiency with class 1 variants may not be diagnosed solely by red cell enzyme assay. Int J Hematol. 2000;71(suppl 1):189.
-
(2000)
Int J Hematol
, vol.71
, Issue.1 SUPPL.
, pp. 189
-
-
Hirono, A.1
Fujii, H.2
Miwa, S.3
-
11
-
-
0029879674
-
Glucose 6-phosphate dehydrogenase mutations causing enzyme deficiency in a model of the tertiary structure of the human enzyme
-
Naylor CE, Rowland P, Basak AK, et al. Glucose 6-phosphate dehydrogenase mutations causing enzyme deficiency in a model of the tertiary structure of the human enzyme. Blood. 1996;87: 2974-2982.
-
(1996)
Blood
, vol.87
, pp. 2974-2982
-
-
Naylor, C.E.1
Rowland, P.2
Basak, A.K.3
-
13
-
-
0030925041
-
Molecular analysis of eight biochemically unique glucose-6-phosphate dehydrogenase variants found in Japan
-
Hirono A, Fujii H, Takano T, Chiba Y, Azuno Y, Miwa S. Molecular analysis of eight biochemically unique glucose-6-phosphate dehydrogenase variants found in Japan. Blood. 1997;89:4624-4627.
-
(1997)
Blood
, vol.89
, pp. 4624-4627
-
-
Hirono, A.1
Fujii, H.2
Takano, T.3
Chiba, Y.4
Azuno, Y.5
Miwa, S.6
-
14
-
-
0028852395
-
Glucose-6-phosphate dehydrogenase mutations and haplotypes in various ethnic groups
-
Xu W, Westwood B, Bartsocas CS, Malcorra-Azpiazu JJ, Indrak K, Beutler E. Glucose-6-phosphate dehydrogenase mutations and haplotypes in various ethnic groups. Blood. 1995;85:257-263.
-
(1995)
Blood
, vol.85
, pp. 257-263
-
-
Xu, W.1
Westwood, B.2
Bartsocas, C.S.3
Malcorra-Azpiazu, J.J.4
Indrak, K.5
Beutler, E.6
-
15
-
-
0028919034
-
New gLucose-6-phosphate dehydrogenase mutations associated with chronic anemia
-
Mason PJ, Sonati MF, MacDonald D, et al. New gLucose-6-phosphate dehydrogenase mutations associated with chronic anemia. Blood. 1995;85:1377-1380.
-
(1995)
Blood
, vol.85
, pp. 1377-1380
-
-
Mason, P.J.1
Sonati, M.F.2
MacDonald, D.3
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