伴有乳酸性酸中毒、范科尼综合征及琥珀酸：细胞色素c还原酶活性缺陷的致命性肝衰竭。 - Suppr

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超能文献

Fatal hepatic failure with lactic acidaemia, Fanconi syndrome and defective activity of succinate:cytochrome c reductase.

作者信息

Vilaseca M A, Briones P, Ribes A, Carreras E, Llácer A, Querol J

机构信息

Institut de Bioquímica Clínica de la Diputació de Barcelona, Spain.

出版信息

J Inherit Metab Dis. 1991;14(3):285-8. doi: 10.1007/BF01811683.

DOI:10.1007/BF01811683

PMID:1663190

Abstract

摘要

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本文引用的文献

An electron-transport system associated with the outer membrane of liver mitochondria. A biochemical and morphological study.与肝线粒体外膜相关的电子传递系统。一项生化与形态学研究。

J Cell Biol. 1967 Feb;32(2):415-38. doi: 10.1083/jcb.32.2.415.

Eur J Pediatr. 1984 Nov;143(1):67-71. doi: 10.1007/BF00442753.

Lactic acidosis and mitochondrial myopathy associated with deficiency of several components of complex III of the respiratory chain.乳酸酸中毒和线粒体肌病与呼吸链复合体III的几种成分缺乏相关。

Pediatr Res. 1984 Oct;18(10):991-9. doi: 10.1203/00006450-198410000-00017.

A mitochondrial encephalomyopathy: the first case with an established defect at the level of coenzyme Q.一种线粒体脑肌病：首例辅酶Q水平存在明确缺陷的病例。

Eur J Pediatr. 1986 Feb;144(5):441-4. doi: 10.1007/BF00441735.

Differential investigation of the capacity of succinate oxidation in human skeletal muscle.人体骨骼肌中琥珀酸氧化能力的差异研究。

Clin Chim Acta. 1985 Nov 29;153(1):23-36. doi: 10.1016/0009-8981(85)90135-4.

Mitochondrial myopathy with lactic acidaemia, Fanconi-De Toni-Debré syndrome and a disturbed succinate: cytochrome c oxidoreductase activity.

Eur J Pediatr. 1988 May;147(4):418-21. doi: 10.1007/BF00496424.

Fatal lactic acidosis in infancy with a defect of complex III of the respiratory chain.伴有呼吸链复合体III缺陷的婴儿期致命性乳酸性酸中毒

Pediatr Res. 1989 May;25(5):553-9. doi: 10.1203/00006450-198905000-00025.

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