Measurement of urinary medium chain acyl glycines by gas chromatography—negative ion chemical ionization mass spectrometry
- 31 December 1991
- journal article
- Published by Elsevier in Journal of Pharmaceutical and Biomedical Analysis
- Vol. 9 (10-12) , 969-975
- https://doi.org/10.1016/0731-7085(91)80032-5
Abstract
No abstract availableKeywords
This publication has 15 references indexed in Scilit:
- Analysis of abnormal urinary metabolites in the newborn period in medium‐chain acyl‐CoA dehydrogenase deficiencyJournal of Inherited Metabolic Disease, 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
- Acylcoenzyme A dehydrogenase deficiency in heart tissue from infants who died unexpectedly with fatty change in the liverBMJ, 1988
- The incidence and presentation of dicarboxylic aciduriaJournal of Inherited Metabolic Disease, 1987
- PRENATAL DIAGNOSIS OF MEDIUM-CHAIN ACYL-CoA DEHYDROGENASE DEFICIENCY IN FAMILY WITH SUDDEN INFANT DEATHThe Lancet, 1987
- The inborn errors of mitochondrial fatty acid oxidationJournal of Inherited Metabolic Disease, 1987
- Pulse oximetry for continuous oxygen monitoring in sick newborn infantsThe 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
- Defects of metabolism of fatty acids in the sudden infant death syndrome.BMJ, 1985