Generalised Dicarboxylic Aciduria: A Common Finding in Neonates
- 1 April 1989
- journal article
- research article
- Published by Wiley in Journal of Inherited Metabolic Disease
- Vol. 12 (S2) , 321-324
- https://doi.org/10.1007/bf03335411
Abstract
No abstract availableKeywords
This publication has 10 references indexed in Scilit:
- PRENATAL DIAGNOSIS OF MEDIUM-CHAIN ACYL-CoA DEHYDROGENASE DEFICIENCY IN FAMILY WITH SUDDEN INFANT DEATHThe Lancet, 1987
- Sudden infant death and inherited disorders of fat oxidation.1986
- Sudden Infant Death and Inherited Disorders of Fat OxidationThe Lancet, 1986
- Genetic Deficiency of Medium-Chain Acyl Coenzyme A Dehydrogenase: Studies in Cultured Skin Fibroblasts and Peripheral Mononuclear LeukocytesPediatric Research, 1985
- Defects of metabolism of fatty acids in the sudden infant death syndrome.BMJ, 1985
- General (medium-chain) acyl-CoA dehydrogenase deficiency (non-ketotic dicarboxylic aciduria): quantitative urinary excretion pattern of 23 biologically significant organic acids in three casesClinica Chimica Acta; International Journal of Clinical Chemistry, 1983
- Concentrations of Organic Acids in the Urine of Healthy Newborn ChildrenAnnals of Clinical Biochemistry: International Journal of Laboratory Medicine, 1978
- Urinary organic acids quantitated by age groups in a healthy pediatric population.Clinical Chemistry, 1977
- LOW MOLECULAR WEIGHT ORGANIC ACIDS IN THE URINE OF THE NEWBORNActa Paediatrica, 1977
- Organic acids in urine from human newborns.Clinical Chemistry, 1976