Deficiency of Dihydrolipoyl Dehydrogenase (a Component of the Pyruvate and α-Ketoglutarate Dehydrogenase Complexes): A Cause of Congenital Chronic Lactic Acidosis in Infancy
- 1 December 1977
- journal article
- research article
- Published by Springer Nature in Pediatric Research
- Vol. 11 (12) , 1198-1202
- https://doi.org/10.1203/00006450-197712000-00006
Abstract
Pediatric Research publishes original papers, invited reviews, and commentaries on the etiologies of diseases of children and disorders of development, extending from molecular biology to epidemiology. Use of model organisms and in vitro techniques relevant to developmental biology and medicine are acceptable, as are translational human studies.Keywords
This publication has 6 references indexed in Scilit:
- [2] Citrate synthase from rat liver: [EC 4.1.3.7 Citrate oxaloacetage-lyase (CoA-acetylating)]Published by Elsevier ,2004
- Lactic Acidosis in Three Sibs Due to Defects in Both Pyruvate Dehydrogenase and α-Ketoglutarate Dehydrogenase ComplexesPediatrics, 1976
- Sensitivity to Carbohydrate in a Patient with Familial Intermittent Lactic Acidosis and Pyruvate Dehydrogenase DeficiencyPediatric Research, 1976
- Colorimetric micro-determination of free fatty acids in plasmaClinica Chimica Acta; International Journal of Clinical Chemistry, 1967
- Lactic acidosis with necrotizing encephalopathy in two sibs.Archives of Disease in Childhood, 1965
- d-(—)-β-HydroxybutyratePublished by Elsevier ,1965