Biochemical and molecular features of deficiencies of Complexes I, II and III-Reference-Cited by-同舟云学术

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Biochemical and molecular features of deficiencies of Complexes I, II and III

Published:1994 Issue: Volume: Page:75-90
ISSN:
Container-title:Mitochondrial Disorders in Neurology
language:
Short-container-title:

Author:

Schapira A.H.V.,Cooper J.M.

Publisher

Elsevier

Reference64 articles.

1. Methods used for the study of normal and abnormal skeletal muscle mitochondria;Sherratt;Methods of Biochemical Analysis,1988

2. Mitochondrial encephalopathies: molecular genetic diagnosis from blood samples;Hammans;Lancet,1991

3. Platelet mitochondrial function in Parkinson's disease;Krige;Annals of Neurology,1992

4. Deletions of mitochondrial DNA in patients with mitochondrial myopathies;Holt;Nature,1988

5. Mitochondrial myopathy with a defect of mitochondrial protein transport;Schapira;New England Journal of Medicine,1990

Cited by 9 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Metabolic myopathies: functional evaluation by different exercise testing approaches;MUSCULOSKELETAL SURGERY;2011-03-04

2. Stress lactate in mitochondrial myopathy under constant, unadjusted workload;European Journal of Neurology;2004-12

3. Lactate Stress Testing in 155 Patients with Mitochondriopathy;Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques;2002-02

4. Phenotype variability in 130 adult patients with respiratory chain disorders;Journal of Inherited Metabolic Disease;2001-10

5. Subcutaneous microdialysis in mitochondrial cytopathy;Muscle & Nerve;2001

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