Propionic acidemia with severe hyperammonemia and defective glycine metabolism
- 1 January 1978
- journal article
- research article
- Published by Elsevier in The Journal of Pediatrics
- Vol. 92 (1), 84-86
- https://doi.org/10.1016/s0022-3476(78)80081-x
Abstract
No abstract availableThis publication has 8 references indexed in Scilit:
- Deficiency of propionyl-CoA carboxylase and methylcrotonyl-CoA carboxylase in a patient with methylcrotonylglycinuriaClinica Chimica Acta; International Journal of Clinical Chemistry, 1977
- Quantitative metabolic profiling of urinary organic acids by gas chromatography-mass spectrometry. Comparison of isolation methodsAnalytical Chemistry, 1975
- Short‐chain organic acidemia and Reye's syndromeNeurology, 1975
- A Block in Glycine Cleavage Reaction as a Common Mechanism in Ketotic and Nonketotic HyperglycinemiaPediatric Research, 1974
- Coexistence of Defective Activity in Glycine-Cleavage Reaction and Propionly-CoA Carboxylase in the Liver of a Hyperglycinemic ChildThe Tohoku Journal of Experimental Medicine, 1974
- Observations on the coexistence of methylmalonic acidemia and glycinemiaThe Journal of Pediatrics, 1969
- Physiological significance of glycine cleavage system in human liver as revealed by the study of a case of hyperglycinemiaBiochemical and Biophysical Research Communications, 1969
- Determination of the Concentration of Ammonia Nitrogen in Plasma by Means of a Simple Ion Exchange MethodAmerican Journal of Clinical Pathology, 1963