Carnitine and Acylcarnitines in Metabolic Disease Diagnosis and Management
- 1 January 1992
- book chapter
- Published by Springer Nature
Abstract
No abstract availableKeywords
This publication has 33 references indexed in Scilit:
- The analysis of diagnostic markers of genetic disorders in human blood and urine using tandem mass spectrometry with liquid secondary ion mass spectrometryInternational Journal of Mass Spectrometry and Ion Processes, 1991
- Mutations in medium chain acyl-CoA dehydrogenase deficiencyThe Lancet, 1990
- Tandem mass spectrometry: A new method for acylcarnitine profiling with potential for neonatal screening for inborn errors of metabolismJournal of Inherited Metabolic Disease, 1990
- Simple and unambiguous method for identifying urinary acylcarnitines using gas chromatography-mass spectrometryThe Analyst, 1990
- Application of continuous-flow liquid chromatography/fast-atom bombardment mass spectrometry to the analysis of diagnostic acylcarnitines in human urineRapid Communications in Mass Spectrometry, 1988
- INVESTIGATION OF INBORN ERRORS OF METABOLISM IN UNEXPECTED INFANT DEATHSThe Lancet, 1988
- Characterization of new diagnostic acylcarnitines in patients with β-ketothiolase deficiency and glutaric aciduria type I using mass spectrometryJournal of Mass Spectrometry, 1987
- Differentiation of isomeric acyl carnitines using tandem mass spectrometryAnalytical Chemistry, 1986
- Carnitine deficiency and hyperammonemia associated with valproic acid therapyThe Journal of Pediatrics, 1982
- Propionylcarnitine physiological variations in vivoBiochimica et Biophysica Acta (BBA) - Lipids and Lipid Metabolism, 1968