Lactic acidemia, neurologic deterioration and carbohydrate dependence in a girl with dihydrolipoyl dehydrogenase deficiency
- 1 March 1981
- journal article
- research article
- Published by Springer Nature in European Journal of Pediatrics
- Vol. 136 (1) , 35-39
- https://doi.org/10.1007/bf00441708
Abstract
No abstract availableKeywords
This publication has 23 references indexed in Scilit:
- Lipoamide dehydrogenase in cultured human skin fibroblastsClinica Chimica Acta; International Journal of Clinical Chemistry, 1978
- Deficiency of Dihydrolipoyl Dehydrogenase (a Component of the Pyruvate and α-Ketoglutarate Dehydrogenase Complexes): A Cause of Congenital Chronic Lactic Acidosis in InfancyPediatric Research, 1977
- Hereditary Mitochondrial Myopathy with Lactic Acidemia, A DeToni-Fanconi-Debr?? Syndrome, and a Defective Respiratory Chain in Voluntary Striated MusclesPediatric Research, 1977
- Biochemical Genetics of the -Keto Acid Dehydrogenase Complexes of Escherichia coli K12: Isolation and Biochemical Properties of Deletion MutantsJournal of General Microbiology, 1977
- The Development of Pyruvate Dehydrogenase in the Subhuman Primate Macaca mulattaNeonatology, 1977
- TWO CASES OF PHOSPHOENOLPYRUVATE CARBOXYKINASE DEFICIENCYActa Paediatrica, 1976
- Absence of Pyruvate Decarboxylase Activity in Man: A Cause of Congenital Lactic AcidosisScience, 1975
- Hepatic fructose-1,6-diphosphatase deficiencyJournal of Clinical Investigation, 1972
- A defect in pyruvate decarboxylase in a child with an intermittent movement disorderJournal of Clinical Investigation, 1970
- SUBACUTE NECROTIZING ENCEPHALOMYELOPATHY IN AN INFANTJournal of Neurology, Neurosurgery & Psychiatry, 1951