Journal of Mass Spectrometry · 1983 · 10 citations · 23 references
Life SciencesBiochemistryClinical BiochemistryEnzymologyMetabolismAmino Acid Metabolism DisordersEnzyme DeficienciesMetabolic DisordersMetabolic Pathway DefectsKetone Body OxidationOrganic AcidemiasPropionic Acidemia
By gas chromatographic mass spectrometric analysis, 3-hydroxy-3-ethylglutaric acid was identified in the urine of patients with propionyl CoA carboxylase deficiency. Simultaneously, large amounts of 3-hydroxyvaleric acid and 3-oxovaleric acid, as well as a number of metabolites previously well known in this disorder, were also found in the urine of the patients. It is suggested that formation of 3-oxovaleric acid and 3-hydroxyvaleric acid proceeds via 3-hydroxy-3-ethylglutaryl CoA as an intermediate by a mechanism similar to that of ketone body formation.
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Propionicacidemia, a New Inborn Error of Metabolism
F.A. Hommes, Jrg Kuipers, J. D. Elema et al. · Pediatric Research · 1968 · 163 citations · Full text
John Diekman, James B. Thomson, Carl Djerassi · The Journal of Organic Chemistry · 1967 · 110 citations
Mass spectrometry of aldonic and deoxyaldonic acids as trimethylsilyl derivatives
G. Petersson · Tetrahedron · 1970 · 108 citations
Pharmacy, Biochemistry, Chemistry +13