Routine gas chromatographic/mass spectrometric analysis of urinary organic acids. Results over a three-year period
- 1 November 1987
- journal article
- research article
- Published by Wiley in Journal of Mass Spectrometry
- Vol. 14 (11) , 663-668
- https://doi.org/10.1002/bms.1200141117
Abstract
No abstract availableKeywords
This publication has 17 references indexed in Scilit:
- Seven years of experience with selective screening for organic aciduriasEuropean Journal of Pediatrics, 1984
- The Routine Investigation of Urinary Organic Acids in Selected Paediatric Patients: Results over a 2 1/2-Year PeriodAnnals of Clinical Biochemistry: International Journal of Laboratory Medicine, 1984
- GC-MS identification of urinary succinylacetone in two cases of hereditary tyrosinaemiaJournal of Inherited Metabolic Disease, 1982
- Organic Acidurias: Approach, Results and Clinical RelevancePublished by Wiley ,1982
- 3-Hydroxy-3-methylglutaric aciduria combined with 3-methylglutaconic aciduria: A new caseJournal of Inherited Metabolic Disease, 1981
- Biochemical study of four cases of propionic acidaemia: GC/MS study of urinary metabolitesJournal of Inherited Metabolic Disease, 1981
- Screening for organic acidurias and amino acidopathies in newborns and childrenJournal of Inherited Metabolic Disease, 1979
- Propionicacidemia, a New Inborn Error of MetabolismPediatric Research, 1968
- Methylmalonic aciduria. An inborn error of metabolism leading to chronic metabolic acidosis.Archives of Disease in Childhood, 1967
- Isovaleric acidemia: a new genetic defect of leucine metabolism.Proceedings of the National Academy of Sciences, 1966