Inborn errors of metabolism leading to lacticacidemia
- 30 April 1982
- journal article
- review article
- Published by Elsevier in Trends in Biochemical Sciences
- Vol. 7 (4) , 151-153
- https://doi.org/10.1016/0968-0004(82)90209-2
Abstract
No abstract availableKeywords
This publication has 10 references indexed in Scilit:
- Lactic acidemia, neurologic deterioration and carbohydrate dependence in a girl with dihydrolipoyl dehydrogenase deficiencyEuropean Journal of Pediatrics, 1981
- How proteins are transported into mitochondriaTrends in Biochemical Sciences, 1981
- The Genetic Heterogeneity of Lactic Acidosis: Occurrence of Recognizable Inborn Errors of Metabolism in a Pediatric Population with Lactic AcidosisPediatric Research, 1980
- Biotin-response OrganicaciduriaJournal of Clinical Investigation, 1979
- Pyruvate Carboxylase and Phosphoenolpyruvate Carboxykinase Activity in Leukocytes and Fibroblasts from a Patient with Pyruvate Carboxylase DeficiencyPediatric Research, 1979
- A possible mechanism for selective cerebellar damage in partial pyruvate dehydrogenase deficiencyNeurology, 1976
- Gene-Protein Relationships of the -Keto Acid Dehydrogenase Complexes of Escherichia coli K12: Chromosomal Location of the Lipoamide Dehydrogenase GeneJournal of General Microbiology, 1974
- Developmental Changes of Cerebral Ketone Body Utilization in Human InfantsBiological Chemistry, 1974
- Studies on pyruvate carboxylase in rat and human liverBiochimica et Biophysica Acta (BBA) - General Subjects, 1970
- Splanchnic removal of lactate and pyruvate during prolonged exercise in manJournal of Applied Physiology, 1966