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A DUAL HEREDITARY RED BLOOD CELL DEFECT IN ONE FAMILY: HYPOCATALASEMIA AND GLUCOSE-6-PHOSPHATE DEHYDROGENASE DEFICIENCY.

作者信息

SZEINBERG A, DE VRIES A, PINKHAS J, DJALDETTI M, EZRA R

出版信息

Acta Genet Med Gemellol (Roma). 1963 Jul;12:247-55. doi: 10.1017/s1120962300016231.

DOI:10.1017/s1120962300016231
PMID:14075877
Abstract
摘要

相似文献

1
A DUAL HEREDITARY RED BLOOD CELL DEFECT IN ONE FAMILY: HYPOCATALASEMIA AND GLUCOSE-6-PHOSPHATE DEHYDROGENASE DEFICIENCY.一个家族中的双遗传性红细胞缺陷：过氧化氢酶缺乏症和葡萄糖-6-磷酸脱氢酶缺乏症。
Acta Genet Med Gemellol (Roma). 1963 Jul;12:247-55. doi: 10.1017/s1120962300016231.
2
OXIDATIVE HEMOLYSIS AND ERYTHROCYTE METABOLISM IN HEREDITARY ACATALASIA.遗传性无过氧化氢酶血症中的氧化溶血与红细胞代谢
J Clin Invest. 1965 Jul;44(7):1187-99. doi: 10.1172/JCI105225.
3
[GLUCOSE-6-PHOSPHATE DEHYDROGENASE DEFECT OF ERYTHROCYTES. (SCREENING TESTS; ACUTE HEMOLYTIC ANEMIA)].[红细胞葡萄糖-6-磷酸脱氢酶缺陷。（筛查试验；急性溶血性贫血）]
Orv Hetil. 1964 Dec 6;105:2318-21.
4
[GLUCOSE-6-PHOSPHATE DEHYDROGENASE DEFICIENCY IN ERYTHROCYTES OF A POLISH FAMILY].[一个波兰家庭红细胞中的葡萄糖-6-磷酸脱氢酶缺乏症]
Pol Arch Med Wewn. 1964;34:93-7.
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CHRONIC HEMOLYSIS ASSOCIATED WITH GLUCOSE-6-PHOSPHATE DEHYDROGENASE DEFICIENCY.与葡萄糖-6-磷酸脱氢酶缺乏相关的慢性溶血
J Lab Clin Med. 1964 Jun;63:1002-9.
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[ON A CASE OF HEMOLYTIC ANEMIA DUE TO SULFAMETHOXYPYRIDAZINE IN A SUBJECT WITH ERYTHROCYTE GLUCOSE-6-PHOSPHATE DEHYDROGENASE DEFICIENCY].[一例红细胞葡萄糖-6-磷酸脱氢酶缺乏患者因磺胺甲氧嗪导致溶血性贫血的病例]
Clin Pediatr (Bologna). 1963 Dec;45:963-71.
7
HEREDITARY HEMOLYTIC DISEASE SECONDARY TO GLUCOSE-6-PHOSPHATE DEHYDROGENASE DEFICIENCY: REPORT OF THREE CASES WITH SPECIAL EMPHASIS ON ATP METABOLISM.葡萄糖-6-磷酸脱氢酶缺乏所致的遗传性溶血性疾病：三例报告并特别强调ATP代谢
Blood. 1964 Apr;23:427-44.
8
[HEMOLYTIC ANEMIA CAUSED BY ENZYMATIC DEFECT (GLUCOSE-6-PHOSPHATE DEHYDROGENASE DEFICIENCY). RESEARCH IN CHILEAN POPULATIONS: MAPUCHE, PASCUENSE AND ALACALUFE].[酶缺陷（葡萄糖-6-磷酸脱氢酶缺乏症）引起的溶血性贫血。智利人群的研究：马普切人、复活节岛人及阿拉卡卢夫族人]
Rev Med Chil. 1964 Aug;92:592-600.
9
"COMPLETE" ERYTHROCYTE GLUCOSE-6-PHOSPHATE DEHYDROGENASE DEFICIENCY.“完全性”红细胞葡萄糖-6-磷酸脱氢酶缺乏症
Arch Intern Med. 1964 Mar;113:428-34. doi: 10.1001/archinte.1964.00280090114019.
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[CHRONIC HEMOLYTIC ANEMIA WITH GLUCOSE-6-PHOSPHATE DEHYDROGENASE DEFICIENCY].[葡萄糖-6-磷酸脱氢酶缺乏所致慢性溶血性贫血]
Bull Mem Soc Med Hop Paris. 1964;115:467-74.

引用本文的文献

1
Catalase enzyme mutations and their association with diseases.过氧化氢酶基因突变及其与疾病的关联。
Mol Diagn. 2004;8(3):141-9. doi: 10.1007/BF03260057.
2
Acatalasemia in the mouse and other species.小鼠及其他物种中的无过氧化氢酶血症
Biochem Genet. 1970 Feb;4(1):135-55. doi: 10.1007/BF00484026.
3
Acatalasia discovered by accident during a disk operation.
Arch Orthop Trauma Surg (1978). 1988;107(3):189-90. doi: 10.1007/BF00451603.
4
Acatalasemia.无过氧化氢酶血症
Hum Genet. 1991 Feb;86(4):331-40. doi: 10.1007/BF00201829.
5
Frequency of hypocatalasemia in a sample of Spanish population.西班牙人群样本中低过氧化氢酶血症的发生率。
Experientia. 1975 Jan 15;31(1):56-7. doi: 10.1007/BF01924677.