Medium-chain acyl-CoA dehydrogenase deficiency in two siblings with a Reye-like syndrome
- 1 June 1985
- journal article
- research article
- Published by Elsevier in The Journal of Pediatrics
- Vol. 106 (6), 918-921
- https://doi.org/10.1016/s0022-3476(85)80237-7
Abstract
No abstract availableThis publication has 20 references indexed in Scilit:
- Microdetermination of 2-ketoglutaric acid in plasma and cerebrospinal fluid by capillary gas chromatography mass spectrometry; application to pediatricsJournal of Mass Spectrometry, 1984
- DICARBOXYLIC ACIDURIA DUE TO MEDIUM CHAIN ACYL CoA DEHYDROGENASE DEFECTActa Paediatrica, 1983
- Dicarboxylic Aciduria: Deficient [1- 14 C]Octanoate Oxidation and Medium-Chain Acyl-CoA Dehydrogenase in FibroblastsScience, 1983
- Fasting hypoglycemia resulting from hepatic carnitine palmitoyl transferase deficiencyThe Journal of Pediatrics, 1981
- Systemic Carnitine Deficiency — A Treatable Inherited Lipid-Storage Disease Presenting as Reye's SyndromeNew England Journal of Medicine, 1980
- Systemic carnitine deficiency simulating recurrent Reye syndromeThe Journal of Pediatrics, 1980
- Profiles in altered metabolism. III—(Ω-1)-hydroxyacid excretion in a case of episodic hypoglycemiaJournal of Mass Spectrometry, 1980
- Ethylmalonic-Adipic AciduriaJCI Insight, 1979
- Acetoacetyl CoA thiolase deficiency: A cause of severe ketoacidosis in infancy simulating salicylismThe Journal of Pediatrics, 1979
- β-HYDROXY-β-METHYLGLUTARICACIDURIA PRESENTING AS REYE'S SYNDROMEThe Lancet, 1979