[家族性NADH依赖性高铁血红蛋白还原酶缺乏与红细胞中甘油-1-磷酸脱氢酶活性相关] - Suppr

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超能文献

[Familial deficiency of NADH-dependent methemoglobin-reductase associated with glycerin-1-phosphate-dehydrogenase activity in the erythrocytes].

作者信息

Kübler W, Kuhn H, Mertens H M, Seipel L

出版信息

Klin Wochenschr. 1971 Dec 1;49(23):1294-8. doi: 10.1007/BF01733086.

DOI:10.1007/BF01733086

PMID:5135950

Abstract

摘要

相似文献

[Familial deficiency of NADH-dependent methemoglobin-reductase associated with glycerin-1-phosphate-dehydrogenase activity in the erythrocytes].[家族性NADH依赖性高铁血红蛋白还原酶缺乏与红细胞中甘油-1-磷酸脱氢酶活性相关]

Klin Wochenschr. 1971 Dec 1;49(23):1294-8. doi: 10.1007/BF01733086.

[Enterogenons methemoglobinemia caused by heterozygotic deficiency of erythrocytic NADH-methemoglobin reductase].红细胞NADH-高铁血红蛋白还原酶杂合性缺乏所致肠源性高铁血红蛋白血症

Blut. 1974 Jul;29(1):43-9. doi: 10.1007/BF01631580.

[Erythrocyte metabolism in congenital methemoglobin reductase deficiency].先天性高铁血红蛋白还原酶缺乏症中的红细胞代谢

Klin Wochenschr. 1968 Dec 1;46(23):1260-3. doi: 10.1007/BF01711870.

[Heterozygous NADH-methemoglobin reductase defect with methemoglobinemia in an infant (author's transl)].婴儿杂合子NADH-高铁血红蛋白还原酶缺陷伴高铁血红蛋白血症（作者译）

Z Kinderheilkd. 1973 Nov 19;115(4):273-81.

Rapid method for detection of erythrocyte NADH-methemoglobin reductase deficiency.检测红细胞NADH-高铁血红蛋白还原酶缺乏症的快速方法。

Am J Clin Pathol. 1972 Feb;57(2):186-7. doi: 10.1093/ajcp/57.2.186.

DPNH-methemoglobin reductase deficiency and hereditary methemoglobinemia.二磷酸吡啶核苷酸-高铁血红蛋白还原酶缺乏症与遗传性高铁血红蛋白血症。

Semin Hematol. 1971 Oct;8(4):417-37.

[Glycerin-1-P-dehydrogenase activity in erythrocytes causing hemolysis].[导致溶血的红细胞中甘油磷酸脱氢酶活性]

Wien Klin Wochenschr. 1970 Oct 18;82(42):763-5.

[Familial NADH diaphorase deficiency].[家族性烟酰胺腺嘌呤二核苷酸黄递酶缺乏症]

Nouv Rev Fr Hematol. 1972 Jul-Aug;12(4):560-3.

Methemoglobinemia provoked by malarial chemoprophylaxis in Vietnam.越南疟疾化学预防引发的高铁血红蛋白血症

N Engl J Med. 1968 Nov 21;279(21):1127-31. doi: 10.1056/NEJM196811212792102.

[Congenital deficiency of erythrocyte NADH-dependent methemoglobin reductase (diaphorase)].[先天性红细胞NADH依赖性高铁血红蛋白还原酶（黄递酶）缺乏症]

Sangre (Barc). 1984;29(1):62-6.

本文引用的文献

Familial idiopathic methaemoglobinaemia and its treatment with ascorbic acid.

Clin Sci. 1945;5(3-4):145-57.

[Sensitive photometric method for the determination of hemoglobin and hemoglobin].用于测定血红蛋白和血红蛋白的灵敏光度法。

Naunyn Schmiedebergs Arch Exp Pathol Pharmakol. 1947;204(1-3):190-202.

[About chronic familial methemoglobinemia and a new modification of methemoglobin].[关于慢性家族性高铁血红蛋白血症及高铁血红蛋白的一种新变体]

Dtsch Med Wochenschr. 1948 Oct 15;73(39-40):476-8. doi: 10.1055/s-0028-1118186.

The reduction of methaemoglobin in red blood cells and studies on the cause of idiopathic methaemoglobinaemia.红细胞中高铁血红蛋白的减少及特发性高铁血红蛋白血症病因的研究

Biochem J. 1948;42(1):13-23. doi: 10.1042/bj0420013.

The relation of diaphorase of human erythrocytes to inheritance of methemoglobinemia.人红细胞黄递酶与高铁血红蛋白血症遗传的关系。

J Clin Invest. 1960 Jul;39(7):1176-9. doi: 10.1172/JCI104131.

The reduction of methemoglobin in human erythrocytes incubated with purine nucleosides.与嘌呤核苷一起孵育的人体红细胞中亚铁血红蛋白的减少。

J Clin Invest. 1959 Sep;38(9):1555-63. doi: 10.1172/JCI103934.

Hereditary hemolytic disorders associated with abnormal hemoglobins.

Am J Med. 1955 Apr;18(4):633-52. doi: 10.1016/0002-9343(55)90464-2.

HEREDITARY METHEMOGLOBINEMIC CYANOSIS IN A MAN WITH ATRIAL SEPTAL DEFECT.

Can Med Assoc J. 1965 Feb 27;92(9):468-70.

[A NEW CASE OF RECESSIVE CONGENITAL METHEMOGLOBINEMIA LINKED WITH A DIAPHORASE I DEFICIENCY].

Arch Fr Pediatr. 1964 Dec;21:1197-204.

HEREDITARY METHEMOGLOBINEMIA DUE TO DIAPHORASE DEFICIENCY IN NAVAJO INDIANS.纳瓦霍印第安人因黄递酶缺乏导致的遗传性高铁血红蛋白血症。

J Pediatr. 1964 Dec;65:928-31. doi: 10.1016/s0022-3476(64)80017-2.

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