Defect in fatty acid oxidation: Laboratory and pathologic findings in a patient
- 30 April 1991
- journal article
- Published by Elsevier in Pediatric Neurology
- Vol. 7 (2) , 125-130
- https://doi.org/10.1016/0887-8994(91)90009-a
Abstract
No abstract availableKeywords
This publication has 21 references indexed in Scilit:
- Medium-Chain Acyl-CoA Dehydrogenase DeficiencyNew England Journal of Medicine, 1988
- The inborn errors of mitochondrial fatty acid oxidationJournal of Inherited Metabolic Disease, 1987
- Complementation analysis of fatty acid oxidation disorders.Journal of Clinical Investigation, 1987
- Medium-chain and long-chain acyl CoA dehydrogenase deficiency: Clinical, pathologic and ultrastructural differentiation from Reye's syndrome†Hepatology, 1986
- Serum dicarboxylic acids in patients with Reye syndromeThe Journal of Pediatrics, 1986
- Recognition of medium-chain acyl-CoA dehydrogenase deficiency in asymptomatic siblings of children dying of sudden infant death or Reye-like syndromesThe Journal of Pediatrics, 1986
- Short-Chain Acyl-CoA Dehydrogenase Deficiency Associated with a Lipid-Storage Myopathy and Secondary Carnitine DeficiencyNew England Journal of Medicine, 1984
- A new patient with dicarboxylic aciduria suggestive of medium-chain acyl-CoA dehydrogenase deficiency presenting as Reye's syndromeJournal of Inherited Metabolic Disease, 1984
- Deficiency of medium chain fatty acylcoenzyme A dehydrogenase presenting as the sudden infant death syndrome.BMJ, 1984
- Glutaric acidemia type II: Clinical, biochemical, and morphologic considerationsThe Journal of Pediatrics, 1982