Focal cytochrome c oxidase deficiency in the brain and dorsal root ganglia in a case with mitochondrial encephalomyopathy (tRNAIle 4269 mutation): histochemical, immunohistochemical, and ultrastructural study
Open Access
- 31 August 1995
- journal article
- Published by Elsevier in Journal of the Neurological Sciences
- Vol. 131 (2) , 170-176
- https://doi.org/10.1016/0022-510x(95)00111-e
Abstract
No abstract availableKeywords
This publication has 17 references indexed in Scilit:
- Strongly succinate dehydrogenase–reactive blood vessels in muscles from patients with mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke‐like episodesAnnals of Neurology, 1991
- MYOCLONUS EPILEPSY AND RAGGED-RED FIBRES (MERRF)Brain, 1989
- Findings in muscle in complex I (NADH coenzyme Q reductase) deficiencyAnnals of Neurology, 1988
- A partial deficiency of cytochrome c oxidase in chronic progressive external ophthalmoplegiaJournal of the Neurological Sciences, 1983
- Mitochondrial myopathy and cardiomyopathy with neurodegenerative features and multiple brain infarctsJournal of the Neurological Sciences, 1982
- Myoclonus epilepsy associated with ragged-red fibres (mitochondrial abnormalities): Disease entity or a syndrome?Journal of the Neurological Sciences, 1980
- Spongy Degeneration of the CNSArchives of Neurology, 1979
- Cerebral spongy degeneration of infancyNeurology, 1972
- SUBACUTE NECROTIZING ENCEPHALOMYELOPATHY: A REVIEW AND A STUDY OF TWO FAMILIESBrain, 1971
- Spongiform encephalopathy with chronic progressive external ophthalmoplegiaNeurology, 1966