Intracerebral distribution of mitochondrial abnormalities in 21 cases of infantile spongy dystrophy
- 1 January 1990
- journal article
- research article
- Published by Elsevier in Journal of the Neurological Sciences
- Vol. 95 (1) , 49-62
- https://doi.org/10.1016/0022-510x(90)90116-5
Abstract
No abstract availableKeywords
This publication has 53 references indexed in Scilit:
- Cytochromec oxidase deficiency in three patients with Leigh's diseaseJournal of Inherited Metabolic Disease, 1988
- Aspartoacylase deficiency and N‐acetylaspartic aciduria in patients with canavan diseaseAmerican Journal of Medical Genetics, 1988
- Clinical presentation of mitochondrial respiratory chain defects in NADH-coenzyme Q reductase and cytochrome oxidase: Clues to pathogenesis of Leigh diseaseThe Journal of Pediatrics, 1987
- N‐acetylaspartic aciduria due to aspartoacylase deficiency — a new aetiology of childhood leukodystrophyJournal of Inherited Metabolic Disease, 1986
- Cortical Subacute Necrotizing EncephalomyelopathyNeuropediatrics, 1984
- Familial subacute necrotizing encephalomyelopathy of the adult form (adult Leigh syndrome)Annals of Neurology, 1979
- Mitochondrial metabolism following bilateral cerebral ischemia in the gerbilAnnals of Neurology, 1977
- Relapsing Form of Subacute Necrotizing EncephalomyelopathyNeuropediatrics, 1973
- Neurodegenerative disorders and hyperaldosteronismThe Journal of Pediatrics, 1971
- Subacute necrotising encephalomyelopathyThe Journal of Pathology and Bacteriology, 1960