Ultrasonography and magnetic resonance imaging in Leigh disease
- 1 September 1990
- journal article
- case report
- Published by Elsevier in Pediatric Neurology
- Vol. 6 (5) , 326-329
- https://doi.org/10.1016/0887-8994(90)90025-v
Abstract
No abstract availableKeywords
This publication has 26 references indexed in Scilit:
- 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
- Cytochrome C oxidase deficiency in two siblings with leigh encephalomyelopathyBrain & Development, 1984
- Enzymologic Studies and Therapy of Leigh's Disease Associated with Pyruvate Decarboxylase DeficiencyPediatric Research, 1982
- Abnormal activation of private dehydrogenase in Leigh disease fibroblastsNeurology, 1982
- Pyruvate Decarboxylase Deficiency in Subacute Necrotizing EncephalomyelopathyArchives of Neurology, 1981
- Defective activation of the pyruvate dehydrogenase complex in subacute necrotizing encephalomyelopathy (leigh disease)Annals of Neurology, 1979
- CT scan appearances in Leigh's disease (subacute necrotizing encephalomyelopathy)Neuroradiology, 1978
- Subacute Necrotizing Encephalomyelopathy (Leigh's Disease): a Consideration of Clinical Features and EtiologyDevelopmental Medicine and Child Neurology, 1972
- SUBACUTE NECROTIZING ENCEPHALOMYELOPATHY: A REVIEW AND A STUDY OF TWO FAMILIESBrain, 1971
- SUBACUTE NECROTIZING ENCEPHALOMYELOPATHY IN AN INFANTJournal of Neurology, Neurosurgery & Psychiatry, 1951