Progression from MERRF to MELAS phenotype in a patient with combined respiratory complex I and IV deficiencies
- 1 December 1988
- journal article
- research article
- Published by Elsevier in Journal of the Neurological Sciences
- Vol. 88 (1-3), 327-337
- https://doi.org/10.1016/0022-510x(88)90229-8
Abstract
No abstract availableThis publication has 30 references indexed in Scilit:
- MITOCHONDRIAL MYOPATHY, ENCEPHALOPATHY, LACTIC ACIDOSIS AND STROKE-LIKE EPISODES (MELAS): ADOLESCENT ONSET WITH SEVERE CEREBRAL EDEMAAustralian and New Zealand Journal of Medicine, 1988
- Mitochondrial studies in Kearns‐Sayre syndromeNeurology, 1987
- Mitochondrial myoneuropathy with respiratory failure and myoclonic epilepsyJournal of the Neurological Sciences, 1985
- Partial cytochrome oxidase (aa3) deficiency in chronic progressive external ophthalmoplegiaJournal of the Neurological Sciences, 1985
- Oxygen electrode studies with human skeletal muscle mitochondria in vitroJournal of the Neurological Sciences, 1985
- Mitochondrial myopathiesAnnals of Neurology, 1985
- NADH-CoQ REDUCTASE DEFICIENT MYOPATHY: SUCCESSFUL TREATMENT WITH RIBOFLAVINThe Lancet, 1983
- HISTORICAL AND CURRENT CONCEPTS IN MITOCHONDRIAL MYOPATHIESAustralian and New Zealand Journal of Medicine, 1983
- Myoclonus epilepsy associated with ragged-red fibres (mitochondrial abnormalities): Disease entity or a syndrome?Journal of the Neurological Sciences, 1980
- Lumping or splitting? “ophthalmoplegia‐plus” or kearns‐sayre syndrome?Annals of Neurology, 1977