Cerebral white matter disease in children may be caused by mitochondrial respiratory chain deficiency
- 1 February 2000
- journal article
- research article
- Published by Elsevier in The Journal of Pediatrics
- Vol. 136 (2) , 209-214
- https://doi.org/10.1016/s0022-3476(00)70103-x
Abstract
No abstract availableKeywords
This publication has 15 references indexed in Scilit:
- Cerebral nuclear magnetic resonance (MRI) in Kearns syndromeActa Ophthalmologica, 2009
- Deletion of mitochondrial DNA in patient with chronic tubulointerstitial nephritisThe Journal of Pediatrics, 1995
- Deficiency in complex IV (cytochrome c oxidase) of the respiratory chain, presenting as a leukodystrophy in two siblings with Leigh syndromeBrain & Development, 1995
- Progressive brainstem and white matter lesions in Kearns—Sayre syndrome: a case reportBrain & Development, 1994
- Biochemical and molecular investigations in respiratory chain deficienciesClinica Chimica Acta; International Journal of Clinical Chemistry, 1994
- The inherited leukodystrophies: A clinical overviewJournal of Inherited Metabolic Disease, 1993
- Deficiency in complex II of the respiratory chain, presenting as a leukodystrophy in two sisters with leigh syndromeBrain & Development, 1992
- Cytochrome c oxidase-associated Leigh syndrome: Phenotypic features and pathogenetic speculationsJournal of the Neurological Sciences, 1991
- Cytochrome c oxidase deficiency in subacute necrotizing encephalopathy (Leigh syndrome)Journal of Inherited Metabolic Disease, 1988
- de Toni-Fanconi-Debré syndrome with leigh syndrome revealing severe muscle cytochrome c oxidase deficiencyThe Journal of Pediatrics, 1988