Studies on a child suspected of having a deficiency in 3-hydroxy-3-methylglutaryl-CoA lyase
- 1 July 1979
- journal article
- research article
- Published by Elsevier in Clinica Chimica Acta; International Journal of Clinical Chemistry
- Vol. 95 (1) , 11-16
- https://doi.org/10.1016/0009-8981(79)90330-9
Abstract
No abstract availableThis publication has 8 references indexed in Scilit:
- Organic acid excretion in a patient with 3-hydroxy-3-methylglutaryl-Coa lyase deficiency: Facts and artefactsClinica Chimica Acta; International Journal of Clinical Chemistry, 1978
- The urinary organic acid profile associated with 3-hydroxy-3-methylglutaric aciduriaClinica Chimica Acta; International Journal of Clinical Chemistry, 1976
- 3-hydroxy-3-methylglutaric aciduria: Deficiency of 3-hydroxy-3-methylglutaryl coenzyme a lyaseClinica Chimica Acta; International Journal of Clinical Chemistry, 1976
- 3-Hydroxy-3-methylglutaric aciduria, combined with 3-methylglutaconic aciduriaClinica Chimica Acta; International Journal of Clinical Chemistry, 1976
- Quantitative metabolic profiling of urinary organic acids by gas chromatography-mass spectrometry. Comparison of isolation methodsAnalytical Chemistry, 1975
- Studies on the urinary acidic metabolites excreted by patients with β-methylcrotonylglycinuria, propionic acidaemia and methylmalonic acidaemia, using gas-liquid chromatography and mass spectrometryClinica Chimica Acta; International Journal of Clinical Chemistry, 1974
- Identification of β-hydroxyisovaleric acid in the urine of a patient with isovaleric acidemiaBiochimica et Biophysica Acta (BBA) - Lipids and Lipid Metabolism, 1968