Approach to diagnosis of oxidative metabolism disorders
- 30 April 1993
- journal article
- review article
- Published by Elsevier in Pediatric Neurology
- Vol. 9 (2) , 81-90
- https://doi.org/10.1016/0887-8994(93)90041-a
Abstract
No abstract availableKeywords
This publication has 25 references indexed in Scilit:
- Molecular genetic and clinical aspects of mitochondrial disorders in childhoodMitochondrion, 2007
- Lethal Neonatal Multiorgan Deficiency of Carnitine Palmitoyltransferase IINew England Journal of Medicine, 1991
- Chronic cardiomyopathy and weakness or acute coma in children with a defect in carnitine uptakeAnnals of Neurology, 1991
- Prevalence of K329E mutation in medium-chain acyl-CoA dehydrogenase gene determined from Guthrie cardsThe Lancet, 1991
- Medium-Chain Acyl-CoA Dehydrogenase DeficiencyNew England Journal of Medicine, 1988
- Lactic acidosis in childhood: Part IIPediatric Neurology, 1986
- Lactic acidosis in childhood: Part IPediatric Neurology, 1985
- Holes in the BrainDevelopmental Medicine and Child Neurology, 1985
- Independence of Blood and Cerebrospinal Fluid LactateArchives of Neurology, 1967
- SUBACUTE NECROTIZING ENCEPHALOMYELOPATHY IN AN INFANTJournal of Neurology, Neurosurgery & Psychiatry, 1951