LOCALISATION OF ENZYMIC DEFECT IN PROPIONICACIDÆMIA
- 30 May 1970
- journal article
- Published by Elsevier BV in The Lancet
- Vol. 295 (7657), 1140-1143
- https://doi.org/10.1016/s0140-6736(70)91216-x
Abstract
No abstract availableKeywords
This publication has 22 references indexed in Scilit:
- Methylmalonyl CoA as an abnormal substrate for δ-aminolevulinic acid synthetaseClinica Chimica Acta; International Journal of Clinical Chemistry, 1969
- Observations on the coexistence of methylmalonic acidemia and glycinemiaThe Journal of Pediatrics, 1969
- DEFECTIVE PROPIONATE CARBOXYLATION IN KETOTIC HYPERGLYCINÆMIAThe Lancet, 1969
- METHYLMALONIC ACIDEMIA A Disorder Associated with Acidosis, Hyperglycinemia, and HyperlactatemiaActa Paediatrica, 1968
- The measurement of urinary methylmalonic acid by a combination of thin-layer and gas chromatographyClinica Chimica Acta; International Journal of Clinical Chemistry, 1968
- Methylmalonic Acidemia a new inborn error of metabolism which may cause fatal acidosis in the neonatal periodScandinavian Journal of Clinical and Laboratory Investigation, 1967
- Idiopathic hyperglycinemia: Isolation and identification of three previously undescribed urinary ketonesThe Journal of Pediatrics, 1966
- Hyperglycinaemia and Hyperglycinuria in a Newborn InfantArchives of Disease in Childhood, 1964
- Phospholipid and Fatty Acid Characteristics of Erythrocytes in Some Cases of AnaemiaBritish Journal of Haematology, 1964
- Human erythrocyte phosphoglycerides I. Quantification of plasmalogens, fatty acids and fatty aldehydesBiochimica et Biophysica Acta, 1962