Diagnosis of medium-chain acyl-coenzyme A dehydrogenase deficiency in the neonatal period by measurement of medium-chain fatty acids in plasma and filter paper blood samples
Open Access
- 1 September 1990
- journal article
- case report
- Published by Elsevier in The Journal of Pediatrics
- Vol. 117 (3) , 439-442
- https://doi.org/10.1016/s0022-3476(05)81091-1
Abstract
No abstract availableThis publication has 9 references indexed in Scilit:
- Medium-Chain Acyl-CoA Dehydrogenase DeficiencyNew England Journal of Medicine, 1988
- 3-Hydroxyoctanoic aciduria: Identification of a new organic acid in the urine of a patient with non-ketotic hypoglycemiaClinica Chimica Acta; International Journal of Clinical Chemistry, 1988
- Specific methylation of plasma nonesterified fatty acids in a one-step reaction.Journal of Lipid Research, 1988
- Familial Reye-Like Syndrome: A Presentation of Medium-Chain Acyl-Coenzyme A Dehydrogenase DeficiencyPediatrics, 1987
- 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
- Octanoic acidemia and octanoylcarnitine excretion with dicarboxylic aciduria due to defective oxidation of medium-chain fatty acidsThe Journal of Pediatrics, 1985
- Medium-Chain Acyl-CoA Dehydrogenase Deficiency in Children with Non-Ketotic Hypoglycemia and Low Carnitine LevelsPediatric Research, 1983
- An improved and simplified radioisotopic assay for the determination of free and esterified carnitineJournal of Lipid Research, 1976
- METABOLIC RATE AND TEMPERATURE CONTROL IN THE HUMAN BABYBritish Medical Bulletin, 1966