Mitochondrial Myopathies

Overview

Journal BMJ

Specialty General Medicine

Date 1989 Apr 29

PMID 2500160

Citations 3

Authors

A H Schapira

Affiliations

Soon will be listed here.

Citing Articles

Current Management and Emerging Therapies in Multiple System Atrophy.

Burns M, McFarland N Neurotherapeutics. 2020; 17(4):1582-1602.

PMID: 32767032 PMC: 7851250. DOI: 10.1007/s13311-020-00890-x.

Mitochondrial myopathies.

Ross B BMJ. 1989; 298(6688):1644-5.

PMID: 2503165 PMC: 1836904. DOI: 10.1136/bmj.298.6688.1644-c.

Mitochondrial genome: defects, disease, and evolution.

Clarke A J Med Genet. 1990; 27(7):451-6.

PMID: 2395164 PMC: 1017184. DOI: 10.1136/jmg.27.7.451.

References

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Poulton J, Deadman M, Gardiner R . Duplications of mitochondrial DNA in mitochondrial myopathy. Lancet. 1989; 1(8632):236-40. DOI: 10.1016/s0140-6736(89)91256-7. View

Rosing H, Hopkins L, Wallace D, Epstein C, Weidenheim K . Maternally inherited mitochondrial myopathy and myoclonic epilepsy. Ann Neurol. 1985; 17(3):228-37. DOI: 10.1002/ana.410170303. View

Kuhn-Nentwig L, KADENBACH B . 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. Eur J Biochem. 1985; 149(1):147-58. DOI: 10.1111/j.1432-1033.1985.tb08905.x. View

DiMauro S, Bonilla E, Zeviani M, Nakagawa M, DeVivo D . Mitochondrial myopathies. Ann Neurol. 1985; 17(6):521-38. DOI: 10.1002/ana.410170602. View

Petty R, Harding A, Morgan-Hughes J . The clinical features of mitochondrial myopathy. Brain. 1986; 109 ( Pt 5):915-38. DOI: 10.1093/brain/109.5.915. View

Morgan-Hughes J, Cooper J, Schapira A, Hayes D, Clark J . The mitochondrial myopathies. Defects of the mitochondrial respiratory chain and oxidative phosphorylation system. Electroencephalogr Clin Neurophysiol Suppl. 1987; 39:103-14. View

Schapira A, Cooper J, Morgan-Hughes J, Patel S, Cleeter M, Ragan C . Molecular basis of mitochondrial myopathies: polypeptide analysis in complex-I deficiency. Lancet. 1988; 1(8584):500-3. DOI: 10.1016/s0140-6736(88)91296-2. View

Holt I, Harding A, Morgan-Hughes J . Deletions of muscle mitochondrial DNA in patients with mitochondrial myopathies. Nature. 1988; 331(6158):717-9. DOI: 10.1038/331717a0. View

10.

Holt I, Cooper J, Morgan-Hughes J, Harding A . Deletions of muscle mitochondrial DNA. Lancet. 1988; 1(8600):1462. DOI: 10.1016/s0140-6736(88)92273-8. View

11.

Zeviani M, Moraes C, DiMauro S, Nakase H, Bonilla E, Schon E . Deletions of mitochondrial DNA in Kearns-Sayre syndrome. Neurology. 1988; 38(9):1339-46. DOI: 10.1212/wnl.38.9.1339. View

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Harding A, Petty R, Morgan-Hughes J . Mitochondrial myopathy: a genetic study of 71 cases. J Med Genet. 1988; 25(8):528-35. PMC: 1080029. DOI: 10.1136/jmg.25.8.528. View

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Frackowiak R, Herold S, Petty R, Morgan-Hughes J . The cerebral metabolism of glucose and oxygen measured with positron tomography in patients with mitochondrial diseases. Brain. 1988; 111 ( Pt 5):1009-24. DOI: 10.1093/brain/111.5.1009. View

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Clay V, Ragan C . Evidence for the existence of tissue specific isoenzymes of mitochondrial NADH dehydrogenase. Biochem Biophys Res Commun. 1988; 157(3):1423-8. DOI: 10.1016/s0006-291x(88)81034-9. View