Congenital lacticacidemia caused by lipoamide dehydrogenase deficiency with favorable outcome
Author:
Publisher
Elsevier BV
Subject
Pediatrics, Perinatology, and Child Health
Reference11 articles.
1. Lipoamide dehydrogenase deficiency with primary lactic acidosis: favorable response to treatment with oral lipoic acid;Matalon;J PEDIATR,1983
2. Congenital lactic acidosis, α-ketoglutaric aciduria and variant form of maple syrup urine disease due to a single enzyme defect: dihydrolipoyl dehydrogenase deficiency;Munnich;Acta Paediatr Scand,1982
3. Deficiency of dihydrolipoyl dehydrogenase (a component of the pyruvate and α-ketoglutarate dehydrogenase complexes): a cause of congenital chronic lactic acidosis in infancy;Robinson;Pediatr Res,1977
4. Lactic acidemia, neurological deterioration and carbohydrate dependence in a girl with dihydrolipoyl dehydrogenase deficiency;Robinson;Eur J Pediatr,1981
5. Dihydrolipoyl dehydrogenase deficiency: a therapeutic trial with branched-chain amino acid restriction;Sakaguchi;Eur J Pediatr,1986
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