A new syndrome of ketoacidosis in infancy
- 30 September 1971
- journal article
- case report
- Published by Elsevier in The Journal of Pediatrics
- Vol. 79 (3), 413-418
- https://doi.org/10.1016/s0022-3476(71)80149-x
Abstract
No abstract availableKeywords
This publication has 11 references indexed in Scilit:
- FASTING HYPOGLYCÆMIA AND METABOLIC ACIDOSIS ASSOCIATED WITH DEFICIENCY OF HEPATIC FRUCTOSE-1,6-DIPHOSPHATASE ACTIVITYThe Lancet, 1970
- Vitamin B12 dependent methylmalonicaciduria: Defective B12 metabolism in cultured fibroblastsBiochemical and Biophysical Research Communications, 1969
- Observations on the coexistence of methylmalonic acidemia and glycinemiaThe Journal of Pediatrics, 1969
- DEFECTIVE PROPIONATE CARBOXYLATION IN KETOTIC HYPERGLYCINÆMIAThe Lancet, 1969
- Methylmalonic Aciduria: Metabolic Block Localization and Vitamin B 12 DependencyScience, 1968
- The Plasma Aminogram. I. Influence of the Level of Protein Intake and a Comparison of Whole Protein and Amino Acid DietsPediatric Research, 1968
- Methylmalonic aciduria. An inborn error of metabolism leading to chronic metabolic acidosis.Archives of Disease in Childhood, 1967
- NEONATAL DEATH ASSOCIATED WITH ISOVALERICACIDÆMIAThe Lancet, 1967
- Methylmalonic Acidemia a new inborn error of metabolism which may cause fatal acidosis in the neonatal periodScandinavian Journal of Clinical and Laboratory Investigation, 1967
- MAPLE SYRUP URINE DISEASE: BRANCHED-CHAIN KETO-ACIDURIAPediatrics, 1960