南斯拉夫的葡萄糖-6-磷酸脱氢酶（G6PD）缺乏症、异常血红蛋白和地中海贫血。 - Suppr

Suppr

超能文献

Glucose-6-phosphate dehydrogenase (G6PD) deficiency, abnormal haemoglobins, and thalassaemia in Yugoslavia.

作者信息

Fraser G R, Grunwald P, Stamatoyannopoulos G

出版信息

J Med Genet. 1966 Mar;3(1):35-41. doi: 10.1136/jmg.3.1.35.

DOI:10.1136/jmg.3.1.35

PMID:5296509

原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1012891/

Abstract

摘要

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b4b7/1012891/f986bc179314/jmedgene00326-0040-a.jpg

相似文献

Glucose-6-phosphate dehydrogenase (G6PD) deficiency, abnormal haemoglobins, and thalassaemia in Yugoslavia.南斯拉夫的葡萄糖-6-磷酸脱氢酶（G6PD）缺乏症、异常血红蛋白和地中海贫血。

J Med Genet. 1966 Mar;3(1):35-41. doi: 10.1136/jmg.3.1.35.

GLUCOSE-6-PHOSPHATE DEHYDROGENASE (G6PD) DEFICIENCY, THALASSAEMIA, AND ABNORMAL HAEMOGLOBINS IN TAIWAN.台湾地区的葡萄糖-6-磷酸脱氢酶（G6PD）缺乏症、地中海贫血及异常血红蛋白

J Med Genet. 1965 Mar;2(1):18-20. doi: 10.1136/jmg.2.1.18.

Studies of the distribution of haemoglobin E, thalassaemias and glucose-6-phosphate dehydrogenase deficiency in north-eastern Thailand.

Nature. 1967 Apr 29;214(5087):501-2. doi: 10.1038/214501a0.

Haemoglobinopathies, glucose-6-phosphate dehydrogenase deficiency and allied problems in the Indian subcontinent.印度次大陆的血红蛋白病、葡萄糖-6-磷酸脱氢酶缺乏症及相关问题。

Bull World Health Organ. 1966;35(6):837-56.

The incidence of glucose-6-phosphate dehydrogenase deficiency and thalassaemia in Malta.马耳他葡萄糖-6-磷酸脱氢酶缺乏症和地中海贫血的发病率。

Br J Haematol. 1970 Jan;18(1):101-6. doi: 10.1111/j.1365-2141.1970.tb01422.x.

Haemoglobin E and beta-thalassaemia: their distribution in Thailand.血红蛋白E与β地中海贫血：它们在泰国的分布情况。

Ann Hum Genet. 1965 Nov;29(2):151-70. doi: 10.1111/j.1469-1809.1965.tb00511.x.

Haemoglobin variants, beta-thalassaemia and G-6-PD types in Liberia.利比里亚的血红蛋白变体、β地中海贫血和葡萄糖-6-磷酸脱氢酶类型

Hum Hered. 1981;31(6):339-47. doi: 10.1159/000153235.

Abnormal haemoglobins, thalassaemia and G-6-PD enzyme deficiency in Rajasthan (western-India).印度西部拉贾斯坦邦的异常血红蛋白、地中海贫血和葡萄糖-6-磷酸脱氢酶（G-6-PD）缺乏症

Haematologia (Budap). 1991;24(3):153-65.

Abnormal hemoglobins, glucose-6-phosphate dehydrogenase deficiency and hereditary ovalocytosis in the Dayaks of Sarawak.砂拉越达雅克人中的异常血红蛋白、葡萄糖-6-磷酸脱氢酶缺乏症和遗传性椭圆形红细胞增多症。

Hum Hered. 1975;25(4):258-62. doi: 10.1159/000152733.

GLUCOSE-6-PHOSPHATE DEHYDROGENASE (G6PD) DEFICIENCY, THALASSAEMIA, AND ABNORMAL HAEMOGLOBINS IN THE PHILIPPINES.菲律宾的葡萄糖-6-磷酸脱氢酶（G6PD）缺乏症、地中海贫血和异常血红蛋白

J Med Genet. 1964 Dec;1(2):102-6. doi: 10.1136/jmg.1.2.102.

引用本文的文献

Molecular Characterization of Glucose-6-phosphate Dehydrogenase Deficiency in Families from the Republic of Macedonia and Genotype-phenotype Correlation.马其顿共和国家庭中葡萄糖-6-磷酸脱氢酶缺乏症的分子特征及基因型-表型相关性

Med Arch. 2015 Oct;69(5):284-8. doi: 10.5455/medarh.2015.69.284-288. Epub 2015 Oct 4.

The distribution of glucose-6-phosphate dehydrogenase deficiency in Greece.希腊葡萄糖-6-磷酸脱氢酶缺乏症的分布情况。

Am J Hum Genet. 1966 May;18(3):296-308.

G6PD deficiency in two autochthonous Croatian families.两个克罗地亚本地家庭中的葡萄糖-6-磷酸脱氢酶缺乏症

J Med Genet. 1969 Sep;6(3):281-5. doi: 10.1136/jmg.6.3.281.

Haemoglobin Lepore in Cyprus.塞浦路斯的血红蛋白Lepore

J Med Genet. 1975 Sep;12(3):275-9. doi: 10.1136/jmg.12.3.275.

本文引用的文献

[On a case of association of thalassemia and "hereditary persistence of fetal hemoglobin"].[关于一例地中海贫血与“胎儿血红蛋白遗传性持续存在”的关联病例]

Haematologica. 1962;47:353-66.

Types of thalassaemia-trait carriers as revealed by a study of their incidence in Greece.通过对希腊地中海贫血特征携带者发病率的研究揭示的携带者类型。

Br J Haematol. 1962 Jan;8:5-14. doi: 10.1111/j.1365-2141.1962.tb06489.x.

HEREDITARY PERSISTENCE OF FETAL HEMOGLOBIN IN GREECE. A STUDY AND A COMPARISON.希腊胎儿血红蛋白的遗传性持续存在。一项研究与比较。

Blood. 1964 Sep;24:223-40.

MILD GLUCOSE-6-PHOSPHATE DEHYDROGENASE DEFICIENCY IN GREEK MALES.希腊男性中的轻度葡萄糖-6-磷酸脱氢酶缺乏症

Lancet. 1964 Oct 31;2(7366):932-5. doi: 10.1016/s0140-6736(64)90863-3.

A THALASSAEMIC TRAIT IN GIPSIES?吉普赛人中的地中海贫血特质？

Acta Med Scand. 1963 Sep;174:261-3. doi: 10.1111/j.0954-6820.1963.tb07921.x.

Genetical linkage between the loci for glucose-6-phosphate dehydrogenase deficiency and colour-blindness in American Negroes.美国黑人中葡萄糖-6-磷酸脱氢酶缺乏症基因座与色盲基因座之间的遗传连锁

Ann Hum Genet. 1962 Nov;26:107-22. doi: 10.1111/j.1469-1809.1962.tb01316.x.

[A case of thalassemia minor].[一例轻型地中海贫血病例]

Lijec Vjesn. 1962 Jul;84:673-8.

A new hereditary hemoglobinopathy (the Lepore trait) and its interaction with thalassemia trait.一种新的遗传性血红蛋白病（Lepore性状）及其与地中海贫血性状的相互作用。

Blood. 1958 Sep;13(9):835-44.

[A case of erythroblastic hemolytic anemia of Cooley's type].[一例库利氏型幼红细胞性溶血性贫血病例]

Srp Arh Celok Lek. 1952 Dec;80(12):1178-81.

文献AI研究员

20分钟写一篇综述，助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型，支持多种主流文档格式。

立即体验