Diagnosis of Medium Chain Acyl-Coa Dehydrogenase (MCAD) Deficiency in an Asymptomatic Neonate
- 1 May 1990
- journal article
- Published by SAGE Publications in Annals of Clinical Biochemistry: International Journal of Laboratory Medicine
- Vol. 27 (3) , 267-269
- https://doi.org/10.1177/000456329002700314
Abstract
No abstract availableThis publication has 6 references indexed in Scilit:
- Urinary organic acid excretion by babies born before 33 weeks of gestation.Clinical Chemistry, 1989
- Medium-Chain Acyl-CoA Dehydrogenase DeficiencyNew England Journal of Medicine, 1988
- The use of phenylpropionic acid as a loading test for medium-chain acyl-CoA dehydrogenase deficiencyJournal of Inherited Metabolic Disease, 1988
- The inborn errors of mitochondrial fatty acid oxidationJournal of Inherited Metabolic Disease, 1987
- SCREENING SIBLINGS FOR INBORN ERRORS OF FATTY ACID METABOLISM IN FAMILIES WITH A HISTORY OF SUDDEN INFANT DEATHThe Lancet, 1986
- Diagnostic and Therapeutic Implications of Medium-Chain Acylcarnitines in the Medium-Chain Acyl-CoA Dehydrogenase DeficiencyPediatric Research, 1985