Leigh syndrome and partial deficit of cytochrome c oxidase associated with epilepsia partialis continua
- 30 June 1996
- journal article
- case report
- Published by Elsevier in Brain & Development
- Vol. 18 (3), 207-211
- https://doi.org/10.1016/0387-7604(95)00126-3
Abstract
No abstract availableKeywords
This publication has 14 references indexed in Scilit:
- The mutation at nt 8993 of mitochondrial DNA is a common cause of Leigh's syndromeAnnals of Neurology, 1993
- A T-to-G Mutation at Nucleotide Pair 8993 in Mitochondrial DNA in a Patient With Leigh's SyndromeJournal of Child Neurology, 1993
- Maternally inherited Leigh syndromeThe Journal of Pediatrics, 1993
- Diagnosis and Treatment in a Case of Juvenile Subacute Necrotizing Encephalopathy Leigh without Cytochrome c Oxidase DeficiencyEuropean Neurology, 1992
- Cytochrome c oxidase-associated Leigh syndrome: Phenotypic features and pathogenetic speculationsJournal of the Neurological Sciences, 1991
- Complex I (reduced nicotinamide-adenine dinucleotide-coenzyme Q reductase) deficiency in two patients with probable Leigh syndromeThe Journal of Pediatrics, 1990
- 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
- Magnetic resonance imaging in subacute necrotizing encephalomyelopathy (Leigh's disease)Annals of Neurology, 1986
- Mitochondrial myopathy and encephalopathyNeurology, 1983
- SUBACUTE NECROTIZING ENCEPHALOMYELOPATHY IN AN INFANTJournal of Neurology, Neurosurgery & Psychiatry, 1951