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A new G-6-PD variant associated with chronic non-spherocytic haemolytic anaemia in a negro family.

作者信息

Howell E B, Nelson A J, Jones O W

出版信息

J Med Genet. 1972 Jun;9(2):160-4. doi: 10.1136/jmg.9.2.160.

DOI:10.1136/jmg.9.2.160
PMID:5046624
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1469022/
Abstract
摘要

相似文献

1
A new G-6-PD variant associated with chronic non-spherocytic haemolytic anaemia in a negro family.在一个黑人家庭中发现一种与慢性非球形红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。
J Med Genet. 1972 Jun;9(2):160-4. doi: 10.1136/jmg.9.2.160.
2
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Acta Haematol. 1982;68(2):131-5. doi: 10.1159/000206964.
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J Pediatr. 1972 Jun;80(6):1005-9. doi: 10.1016/s0022-3476(72)80014-3.
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[Glucose-6-phosphate dehydrogenase type Schwaben. A new enzyme variant with spontaneous hemolytic anemia].施瓦本型葡萄糖-6-磷酸脱氢酶。一种伴有自发性溶血性贫血的新型酶变体
Dtsch Med Wochenschr. 1971 Jun 11;96(24):1029-33. doi: 10.1055/s-0028-1108377.
5
Red cell glucose-6-phosphate dehydrogenase deficiency in Finland. Further biochemical characterization of G-6-PD Helsinki.芬兰的红细胞葡萄糖-6-磷酸脱氢酶缺乏症。G-6-PD赫尔辛基型的进一步生化特征分析。
Ann Clin Res. 1974 Aug;6(4):187-97.
6
Adenosine-triphosphatase deficiency in a family with non-spherocytic haemolytic anaemia.一个患有非球形红细胞溶血性贫血的家族中的三磷酸腺苷酶缺乏症。
Hum Hered. 1971;21(4):313-9. doi: 10.1159/000152420.
7
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
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Congenital nonspherocytic hemolytic anemia associated with erythrocyte glucose-6-phosphate dehydrogenase deficiency in a Negro family.一个黑人家庭中与红细胞葡萄糖-6-磷酸脱氢酶缺乏相关的先天性非球形细胞溶血性贫血
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Am J Med. 1970 Jul;49(1):125-32. doi: 10.1016/s0002-9343(70)80122-x.
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Three new variants of glucose-6-phosphate dehydrogenase associated with chronic nonspherocytic hemolytic anemia: G-6-PD Lincoln Park, G-6-PD Arlington Heights, and G-6-PD West Town.三种与慢性非球形红细胞溶血性贫血相关的葡萄糖-6-磷酸脱氢酶新变体：葡萄糖-6-磷酸脱氢酶林肯公园型、葡萄糖-6-磷酸脱氢酶阿灵顿高地型和葡萄糖-6-磷酸脱氢酶西城型。
Am J Hematol. 1979;6(4):353-60. doi: 10.1002/ajh.2830060407.

引用本文的文献

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A new glucose-6-phosphate dehydrogenase variant (G6PD Nagano) associated with congenital hemolytic anemia.一种与先天性溶血性贫血相关的新型葡萄糖-6-磷酸脱氢酶变体（G6PD 长野型）
Hum Genet. 1982;62(4):368-70. doi: 10.1007/BF00304560.
2
G-6-PD Guadalajara. A new mutant associated with chronic nonspherocytic hemolytic anemia.
Hum Genet. 1982;61(2):175-6. doi: 10.1007/BF00274214.
3
'Gd(-) Hôtel Dieu': a new G-6PD variant with chronic hemolysis in a Negro patient from Senegal.
Hum Genet. 1977 Dec 23;39(3):353-7. doi: 10.1007/BF00295431.
4
Glucose-6-phosphate dehydrogenase (G6PD) activity of human sperm.人类精子的葡萄糖-6-磷酸脱氢酶（G6PD）活性
J Med Genet. 1977 Aug;14(4):250-5. doi: 10.1136/jmg.14.4.250.

本文引用的文献

1
"CHICAGO I" VARIANT OF GLUCOSE-6-PHOSPHATE DEHYDROGENASE IN CONGENITAL HEMOLYTIC DISEASE.先天性溶血性疾病中葡萄糖-6-磷酸脱氢酶的“芝加哥I”变体
J Lab Clin Med. 1964 May;63:715-25.
2
Improved method for the determination of blood glutathione.测定血液中谷胱甘肽的改进方法。
J Lab Clin Med. 1963 May;61:882-8.
3
Congenital nonspherocytic hemolytic anemia.先天性非球形细胞溶血性贫血
Am J Dis Child. 1961 Sep;102:313-20. doi: 10.1001/archpedi.1961.02080010315006.
4
The hemolytic effect of primaquine and related compounds: a review.伯氨喹及相关化合物的溶血作用：综述
Blood. 1959 Feb;14(2):103-39.
5
A deficiency of glucose-6-phosphate dehydrogenase activity in erythrocytes from patients with favism.蚕豆病患者红细胞中葡萄糖-6-磷酸脱氢酶活性缺乏。
Bull Johns Hopkins Hosp. 1958 Apr;102(4):169-75.
6
Hereditary hemolytic anemia with hexokinase deficiency. Role of hexokinase in erythrocyte aging.伴有己糖激酶缺乏的遗传性溶血性贫血。己糖激酶在红细胞衰老中的作用。
N Engl J Med. 1967 Jan 5;276(1):1-11. doi: 10.1056/NEJM196701052760101.
7
Congenital nonspherocytic hemolytic anemia associated with erythrocyte glucose-6-phosphate dehydrogenase deficiency in a Negro family.一个黑人家庭中与红细胞葡萄糖-6-磷酸脱氢酶缺乏相关的先天性非球形细胞溶血性贫血
Pediatrics. 1966 Apr;37(4):624-9.
8
Anemia, cataracts, and seizures in patient with glucose-6-phosphate dehydrogenase deficiency.葡萄糖-6-磷酸脱氢酶缺乏症患者的贫血、白内障和癫痫发作。
Arch Intern Med. 1966 Oct;118(4):385-90.
9
Evidence for four types of erythrocyte glucose-6-phosphate dehydrogenase from G-6-PD-deficient human subjects.来自葡萄糖-6-磷酸脱氢酶（G-6-PD）缺乏的人类受试者的四种红细胞葡萄糖-6-磷酸脱氢酶类型的证据。
J Clin Invest. 1966 Jun;45(6):823-31. doi: 10.1172/JCI105398.
10
Hereditary hemolytic anemia associated with glucosephosphate isomerase (GPI) deficiency--a new enzyme defect of human erythrocytes.与葡萄糖磷酸异构酶（GPI）缺乏相关的遗传性溶血性贫血——人类红细胞的一种新的酶缺陷。
Blood. 1968 Aug;32(2):236-49.