The lacticacidemias
- 1 January 1985
- book chapter
- Published by Elsevier
Abstract
No abstract availableKeywords
This publication has 83 references indexed in Scilit:
- Lipoamide dehydrogenase deficiency with primary lactic acidosis: Favorable response to treatment with oral lipoic acidThe Journal of Pediatrics, 1984
- Lactic acidosis in biotin-responsive multiple carboxylase deficiency caused by holocarboxylase synthetase deficiency of early and late onsetThe Journal of Pediatrics, 1982
- Amino acid profile in pyruvate carboxylase deficiency: Comparison with some other metabolic disordersJournal of Inherited Metabolic Disease, 1982
- Lipoamide Dehydrogenase DeficiencyNew England Journal of Medicine, 1981
- Kinetic properties of human F4 phosphofructokinaseFEBS Letters, 1980
- Defective activation of the pyruvate dehydrogenase complex in subacute necrotizing encephalomyelopathy (leigh disease)Annals of Neurology, 1979
- Thiamine dependency in a patient with congenital lacticacidaemia due to pyruvate dehydrogenase deficiencyInflammation Research, 1977
- Purification and properties of human liver pyruvate carboxylaseBiochemical Medicine, 1974
- The activity of pyruvate dehydrogenase in rat brain during postnatal developmentFEBS Letters, 1974
- In situ oxidation of lactate by skeletal muscle during intermittent exerciseFEBS Letters, 1970