The treatment of congenital lactic acidoses
- 1 July 1996
- journal article
- review article
- Published by Springer Nature in Journal of Inherited Metabolic Disease
- Vol. 19 (4) , 573-580
- https://doi.org/10.1007/bf01799117
Abstract
No abstract availableKeywords
This publication has 43 references indexed in Scilit:
- Metabolic disorders of embryogenesisJournal of Inherited Metabolic Disease, 1994
- Transient improvement of congenital lactic acidosis in a male infant with pyruvate decarboxylase deficiency treated with dichloroacetateThe Journal of Pediatrics, 1993
- Beneficial effect of sodium dichloroacetate in muscle cytochrome C oxidase deficiencyEuropean Journal of Pediatrics, 1993
- Assessment and therapy monitoring of Leigh disease by MRI and proton spectroscopyPediatric Neurology, 1992
- Thiamine Responsive Pyruvate Dehydrogenase DeficiencyJournal of Nutritional Science and Vitaminology, 1992
- A Mitochondrial Myopathy in an Infant with Lactic AcidosisDevelopmental Medicine and Child Neurology, 1990
- Variable clinical presentation in patients with defective E1 component of pyruvate dehydrogenase complexThe Journal of Pediatrics, 1987
- Benign Mitochondrial Myopathy with Deficiency of NADH-CoQ Reductase and Cytochrome c OxidaseNeuropediatrics, 1986
- Lipoamide dehydrogenase deficiency with primary lactic acidosis: Favorable response to treatment with oral lipoic acidThe Journal of Pediatrics, 1984
- 31P NMR examination of two patients with NADH-CoQ reductase deficiencyNature, 1982