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Mitochondrial myopathies.

作者信息

Schapira A H

出版信息

BMJ. 1989 Apr 29;298(6681):1127-8. doi: 10.1136/bmj.298.6681.1127.

DOI:10.1136/bmj.298.6681.1127
PMID:2500160
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1836412/
Abstract
摘要

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本文引用的文献

1
Mitochondrial encephalomyopathies: biochemical studies in two cases revealing defects in the respiratory chain.线粒体脑肌病：两例生化研究揭示呼吸链缺陷
Brain. 1982 Sep;105 (Pt 3):553-82. doi: 10.1093/brain/105.3.553.
2
Mitochondrial myopathies.线粒体肌病
Ann Neurol. 1985 Jun;17(6):521-38. doi: 10.1002/ana.410170602.
3
Maternally inherited mitochondrial myopathy and myoclonic epilepsy.母系遗传的线粒体肌病和肌阵挛性癫痫。
Ann Neurol. 1985 Mar;17(3):228-37. doi: 10.1002/ana.410170303.
4
The clinical features of mitochondrial myopathy.线粒体肌病的临床特征。
Brain. 1986 Oct;109 ( Pt 5):915-38. doi: 10.1093/brain/109.5.915.
5
Deletions of mitochondrial DNA in Kearns-Sayre syndrome.卡恩斯-塞尔综合征中线粒体DNA的缺失。
Neurology. 1988 Sep;38(9):1339-46. doi: 10.1212/wnl.38.9.1339.
6
The cerebral metabolism of glucose and oxygen measured with positron tomography in patients with mitochondrial diseases.
Brain. 1988 Oct;111 ( Pt 5):1009-24. doi: 10.1093/brain/111.5.1009.
7
Evidence for the existence of tissue specific isoenzymes of mitochondrial NADH dehydrogenase.
Biochem Biophys Res Commun. 1988 Dec 30;157(3):1423-8. doi: 10.1016/s0006-291x(88)81034-9.
8
Mitochondrial myopathy: a genetic study of 71 cases.线粒体肌病：71例的遗传学研究
J Med Genet. 1988 Aug;25(8):528-35. doi: 10.1136/jmg.25.8.528.
9
Isolation and properties of cytochrome c oxidase from rat liver and quantification of immunological differences between isozymes from various rat tissues with subunit-specific antisera.大鼠肝脏细胞色素c氧化酶的分离、性质以及用亚基特异性抗血清对不同大鼠组织同工酶之间免疫差异的定量分析。
Eur J Biochem. 1985 May 15;149(1):147-58. doi: 10.1111/j.1432-1033.1985.tb08905.x.
10
Deletions of muscle mitochondrial DNA.肌肉线粒体DNA的缺失
Lancet. 1988 Jun 25;1(8600):1462. doi: 10.1016/s0140-6736(88)92273-8.