Hereditary coproporphyria. Study of a Swedish family.

Suppr

超能文献

作者信息

Haeger-Aronsen B, Stathers G, Swahn G

出版信息

Ann Intern Med. 1968 Aug;69(2):221-7. doi: 10.7326/0003-4819-69-2-221.

DOI:10.7326/0003-4819-69-2-221

PMID:5667765

Abstract

摘要

相似文献

Hereditary coproporphyria. Study of a Swedish family.

Ann Intern Med. 1968 Aug;69(2):221-7. doi: 10.7326/0003-4819-69-2-221.

Hepatic delta-aminolaevulinic acid synthetase in an attack of hereditary coproporphyria and during remission.

Lancet. 1971 Mar 20;1(7699):560-4. doi: 10.1016/s0140-6736(71)91161-5.

Hereditary coproporphyria. A family with unusually few and mild symptoms.

Acta Med Scand. 1969 Jul-Aug;186(1-2):83-5.

Intermittent acute porphyria--demonstration of a genetic defect in porphobilinogen metabolism.间歇性急性卟啉病——胆色素原代谢遗传缺陷的证明

N Engl J Med. 1972 Jun 15;286(24):1277-82. doi: 10.1056/NEJM197206152862401.

Hereditary coproporphyria. Photosensitivity, jaundice and neuropsychiatric manifestations associated with pregnancy.遗传性粪卟啉病。与妊娠相关的光敏性、黄疸及神经精神症状。

Br J Dermatol. 1971 Apr;84(4):301-10. doi: 10.1111/j.1365-2133.1971.tb14223.x.

Faecal porphyrin excretion in various types of porphyria. Thin layer chromatographic study.

Arch Dermatol Res. 1978;263(1):67-73.

[Hereditary coproporphyria].

Rev Clin Esp. 1968 Jul 15;110(1):81-2.

[Hereditary coproporphyria].

Ugeskr Laeger. 1973 Nov 19;135(47):2571.

[Hereditary coproporphyria in 2 Dutch families].[荷兰两个家族中的遗传性粪卟啉病]

Ned Tijdschr Geneeskd. 1984 May 12;128(19):892-5.

Porphyria cutanea tarda-a genetic disease? A biochemical and fluorescence microscopical study in four families.

Acta Med Scand. 1973 Oct;194(4):265-70.

引用本文的文献

Production and characterization of erythropoietic protoporphyric heterodimeric ferrochelatases.促红细胞生成性原卟啉异二聚体铁螯合酶的产生与特性分析

Blood. 2005 Aug 1;106(3):1098-104. doi: 10.1182/blood-2004-12-4661. Epub 2005 Apr 14.

Hereditary coproporphyria: incidence in a large English family.遗传性粪卟啉病：一个英国家庭中的发病率

J Med Genet. 1984 Oct;21(5):341-9. doi: 10.1136/jmg.21.5.341.

Hereditary coproporphyria: unusual nervous system involvement in two cases.遗传性粪卟啉病：两例不寻常的神经系统受累情况。

J Neurol. 1984;231(2):99-101. doi: 10.1007/BF00313726.

Coexistence of hereditary coproporphyria and epilepsy: coproporphyrinogen oxidase deficiency in liver and kidney.遗传性粪卟啉病与癫痫共存：肝脏和肾脏中粪卟啉原氧化酶缺乏

J Neurol. 1981;226(1):25-33. doi: 10.1007/BF00313315.

The porphyrias: a review.卟啉症综述

J Clin Pathol. 1972 Dec;25(12):1013-33. doi: 10.1136/jcp.25.12.1013.

Hereditary coproporphyria and epilepsy.遗传性粪卟啉病与癫痫

Arch Dis Child. 1977 Aug;52(8):646-50. doi: 10.1136/adc.52.8.646.

Catecholamine uptake, accumulation, and release in acute porphyria.急性卟啉病中儿茶酚胺的摄取、蓄积和释放

J Clin Invest. 1977 Nov;60(5):1141-8. doi: 10.1172/JCI108866.

Aucte intermittent porphyria and epilepsy.急性间歇性卟啉病与癫痫。（注：原文“Aucte”可能有误，推测为“Acute”，翻译按此修正）

Arch Dis Child. 1979 Aug;54(8):644-5. doi: 10.1136/adc.54.8.644.

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