Skip to main content
PMC home page
The BMJ logoLink to The BMJ
. 1989 Apr 29;298(6681):1127–1128. doi: 10.1136/bmj.298.6681.1127

Mitochondrial myopathies.

A H Schapira
PMCID: PMC1836412  PMID: 2500160

Full text

PDF
1127

Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Clay V. J., Ragan C. I. Evidence for the existence of tissue specific isoenzymes of mitochondrial NADH dehydrogenase. Biochem Biophys Res Commun. 1988 Dec 30;157(3):1423–1428. doi: 10.1016/s0006-291x(88)81034-9. [DOI] [PubMed] [Google Scholar]
  2. DiMauro S., Bonilla E., Zeviani M., Nakagawa M., DeVivo D. C. Mitochondrial myopathies. Ann Neurol. 1985 Jun;17(6):521–538. doi: 10.1002/ana.410170602. [DOI] [PubMed] [Google Scholar]
  3. Frackowiak R. S., Herold S., Petty R. K., Morgan-Hughes J. A. The cerebral metabolism of glucose and oxygen measured with positron tomography in patients with mitochondrial diseases. Brain. 1988 Oct;111(Pt 5):1009–1024. doi: 10.1093/brain/111.5.1009. [DOI] [PubMed] [Google Scholar]
  4. Harding A. E., Petty R. K., Morgan-Hughes J. A. Mitochondrial myopathy: a genetic study of 71 cases. J Med Genet. 1988 Aug;25(8):528–535. doi: 10.1136/jmg.25.8.528. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. Holt I. J., Cooper J. M., Morgan-Hughes J. A., Harding A. E. Deletions of muscle mitochondrial DNA. Lancet. 1988 Jun 25;1(8600):1462–1462. doi: 10.1016/s0140-6736(88)92273-8. [DOI] [PubMed] [Google Scholar]
  6. Holt I. J., Harding A. E., Morgan-Hughes J. A. Deletions of muscle mitochondrial DNA in patients with mitochondrial myopathies. Nature. 1988 Feb 25;331(6158):717–719. doi: 10.1038/331717a0. [DOI] [PubMed] [Google Scholar]
  7. 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 May 15;149(1):147–158. doi: 10.1111/j.1432-1033.1985.tb08905.x. [DOI] [PubMed] [Google Scholar]
  8. Morgan-Hughes J. A., Cooper J. M., Schapira A. H., Hayes D. J., Clark J. B. The mitochondrial myopathies. Defects of the mitochondrial respiratory chain and oxidative phosphorylation system. Electroencephalogr Clin Neurophysiol Suppl. 1987;39:103–114. [PubMed] [Google Scholar]
  9. Morgan-Hughes J. A., Hayes D. J., Clark J. B., Landon D. N., Swash M., Stark R. J., Rudge P. Mitochondrial encephalomyopathies: biochemical studies in two cases revealing defects in the respiratory chain. Brain. 1982 Sep;105(Pt 3):553–582. doi: 10.1093/brain/105.3.553. [DOI] [PubMed] [Google Scholar]
  10. Petty R. K., Harding A. E., Morgan-Hughes J. A. The clinical features of mitochondrial myopathy. Brain. 1986 Oct;109(Pt 5):915–938. doi: 10.1093/brain/109.5.915. [DOI] [PubMed] [Google Scholar]
  11. Poulton J., Deadman M. E., Gardiner R. M. Duplications of mitochondrial DNA in mitochondrial myopathy. Lancet. 1989 Feb 4;1(8632):236–240. doi: 10.1016/s0140-6736(89)91256-7. [DOI] [PubMed] [Google Scholar]
  12. Rosing H. S., Hopkins L. C., Wallace D. C., Epstein C. M., Weidenheim K. Maternally inherited mitochondrial myopathy and myoclonic epilepsy. Ann Neurol. 1985 Mar;17(3):228–237. doi: 10.1002/ana.410170303. [DOI] [PubMed] [Google Scholar]
  13. Schapira A. H., Cooper J. M., Morgan-Hughes J. A., Patel S. D., Cleeter M. J., Ragan C. I., Clark J. B. Molecular basis of mitochondrial myopathies: polypeptide analysis in complex-I deficiency. Lancet. 1988 Mar 5;1(8584):500–503. doi: 10.1016/s0140-6736(88)91296-2. [DOI] [PubMed] [Google Scholar]
  14. Zeviani M., Moraes C. T., DiMauro S., Nakase H., Bonilla E., Schon E. A., Rowland L. P. Deletions of mitochondrial DNA in Kearns-Sayre syndrome. Neurology. 1988 Sep;38(9):1339–1346. doi: 10.1212/wnl.38.9.1339. [DOI] [PubMed] [Google Scholar]

Articles from BMJ : British Medical Journal are provided here courtesy of BMJ Publishing Group

RESOURCES