Massive excretion of 2-oxoglutaric acid and 3-hydroxyisovaleric acid in a patient with a deficiency of 3-methylcrotonyl-CoA carboxylase
- 1 December 1976
- journal article
- research article
- Published by Elsevier in Clinica Chimica Acta; International Journal of Clinical Chemistry
- Vol. 73 (3) , 513-519
- https://doi.org/10.1016/0009-8981(76)90155-8
Abstract
No abstract availableThis publication has 11 references indexed in Scilit:
- The occurrence and identification of o-hydroxyhippuric acid (salicyluric acid) in the urine of sick childrenClinica Chimica Acta; International Journal of Clinical Chemistry, 1976
- Beta-methylcrotonic aciduria associated with lactic acidosisThe Journal of Pediatrics, 1976
- Increased urinary excretion of 3-hydroxyisovaleric acid in patients with ketoacidosisClinica Chimica Acta; International Journal of Clinical Chemistry, 1974
- 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
- Child with a defect in leucine metabolism associated with beta-hydroxyisovaleric aciduria and beta-methylcrotonylglycinuria.Archives of Disease in Childhood, 1973
- Determination of α-keto acids as silylated oximes in urine and serum by combined gas chromatography-mass spectrometryClinica Chimica Acta; International Journal of Clinical Chemistry, 1973
- BETA-METHYLCROTONYL-CoA CARBOXYLASE DEFICIENCY: A NEW METABOLIC ERROR IN LEUCINE DEGRADATIONPublished by American Academy of Pediatrics (AAP) ,1972
- BIOTIN-RESPONSIVE β-METHYLCROTONYLGLYCINURIAThe Lancet, 1971
- $beta;-HYDROXYISOVALERIC ACIDURIA AND $beta;-METHYLCROTONYLGLYCINURIA: A NEW INBORN ERROR OF METABOLISMThe Lancet, 1970
- Chronic lactic acidosis of infancyThe Journal of Pediatrics, 1970