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[Deficiency of red cell glucose-6-phosphate-dehydrogenase due to a slow variant in a French family. Relationship with the Gd (-) Seattle variant (author's transl)].

作者信息

Kahn A, Boivin P, Lagneau J, Cruveiller J

出版信息

Nouv Rev Fr Hematol. 1973 Mar-Apr;13(2):163-71.

PMID:4270706
Abstract
摘要

相似文献

1
[Deficiency of red cell glucose-6-phosphate-dehydrogenase due to a slow variant in a French family. Relationship with the Gd (-) Seattle variant (author's transl)].[一个法国家庭中因慢变体型导致的红细胞葡萄糖-6-磷酸脱氢酶缺乏症。与Gd(-)西雅图变体型的关系（作者译）]
Nouv Rev Fr Hematol. 1973 Mar-Apr;13(2):163-71.
2
An Iraqi Jewish family with a new red cell glucose-6-phosphate dehydrogenase variant (GD-Bagdad) and kernicterus.一个患有新型红细胞葡萄糖-6-磷酸脱氢酶变异体（GD-巴格达型）和核黄疸的伊拉克犹太家庭。
Isr J Med Sci. 1973 Aug;9(8):1040-3.
3
[Congenital deficiency in glucose-6-phosphate dehydrogenase. Slow variant found in a Spanish family. Relation with the variant Gd(minus) "Seattle" (author's transl)].
Sangre (Barc). 1974;19(4):435-42.
4
Red cell glucose-6-phosphate dehydrogenase deficiency in Finland.芬兰的红细胞葡萄糖-6-磷酸脱氢酶缺乏症
Ann Clin Res. 1973 Jun;5(3):168-73.
5
Glucose-6-phosphate dehydrogenase slow variant with deficiency in a Spanish family. Relationship with the Gd (minus) Seattle variant.西班牙一家族中葡萄糖-6-磷酸脱氢酶慢变体型伴缺乏症。与Gd（阴性）西雅图变体型的关系。
Biomedicine. 1974 Jul;21(7):303-7.
6
A glucose 6-phosphate dehydrogenase Gd (-) Castilla variant characterized by mild deficiency associated with drug-induced hemolytic anemia.一种葡萄糖6-磷酸脱氢酶Gd（-）卡斯蒂利亚变体，其特征为与药物诱导的溶血性贫血相关的轻度缺乏。
J Lab Clin Med. 1977 Oct;90(4):754-9.
7
[A family of new glucose 6-phosphate dehydrogenase (G 6 PD) variant associated with chronic nonspherocytic hemolytic anemia: G 6 PD Kurume (author's transl)].与慢性非球形细胞溶血性贫血相关的新型葡萄糖6-磷酸脱氢酶（G 6 PD）变异体家族：G 6 PD久留米型（作者译）
Rinsho Ketsueki. 1979 Jan;20(1):82-9.
8
[Results of long-term observations of children with erythrocytic glucosephosphate dehydrogenase deficiency].[红细胞葡萄糖磷酸脱氢酶缺乏症患儿的长期观察结果]
Pol Tyg Lek. 1988;43(18-19):593-7.
9
[Federal District glucose-6-phosphate dehydrogenase Gd(-). A new variant associated with moderate enzyme deficiency and occasional hemolytic anemia].[联邦区葡萄糖-6-磷酸脱氢酶Gd(-)。一种与中度酶缺乏和偶发性溶血性贫血相关的新变体]
Rev Invest Clin. 1981 Apr-Jun;33(2):209-11.
10
[Glucose-6-phosphate dehydrogenase deficiency hereditary hemolytic anemia (author's transl)].葡萄糖-6-磷酸脱氢酶缺乏症遗传性溶血性贫血（作者译）
Lijec Vjesn. 1979 Sep;101(9):560-2.

引用本文的文献

1
Molecular mechanism of glucose-6-phosphate dehydrogenase deficiency.葡萄糖-6-磷酸脱氢酶缺乏症的分子机制。
Humangenetik. 1974;25(2):101-9. doi: 10.1007/BF00283310.
2
G6PD Lozere and Trinacria-like. Segregation of two non hemolytic variants in a French family.
Hum Genet. 1976 Dec 15;34(3):293-8. doi: 10.1007/BF00295293.
3
Three rare G-6-PD variants from Porto Alegre, Brazil.来自巴西阿雷格里港的三种罕见葡萄糖-6-磷酸脱氢酶（G-6-PD）变体。
Hum Genet. 1977 Nov 10;39(2):191-7. doi: 10.1007/BF00287011.