Transient improvement of congenital lactic acidosis in a male infant with pyruvate decarboxylase deficiency treated with dichloroacetate

This publication has 13 references indexed in Scilit:

• Variable clinical presentation in patients with defective E1 component of pyruvate dehydrogenase complex
  The Journal of Pediatrics, 1987
• Lacticacidaemia due to pyruvate dehydrogenase deficiency, with evidence of protein polymorphism in the ?-subunit of the enzyme
  European Journal of Pediatrics, 1986
• Treatment of chronic congenital lactic acidosis by oral administration of dichloroacetate
  Journal of Inherited Metabolic Disease, 1985
• Partial pyruvate decarboxylase deficiency with profound lactic acidosis and hyperammonemia: Responses to dichloroacetate and benzoate
  American Journal of Medical Genetics, 1985
• Treatment of Lactic Acidosis with Dichloroacetate
  New England Journal of Medicine, 1983
• Pyruvate Dehydrogenase Complex Activity in Normal and Deficient Fibroblasts
  Journal of Clinical Investigation, 1981
• Regulation of Mammalian Pyruvate Dehydrogenase Complex by a Phosphorylation–Dephosphorylation Cycle
  Current Topics in Cellular Regulation, 1981
• Absence of Pyruvate Decarboxylase Activity in Man: A Cause of Congenital Lactic Acidosis
  Science, 1975
• Mechanism of activation of pyruvate dehydrogenase by dichloroacetate and other halogenated carboxylic acids
  Biochemical Journal, 1974
• α-KETO ACID DEHYDROGENASE COMPLEXES, X. REGULATION OF THE ACTIVITY OF THE PYRUVATE DEHYDROGENASE COMPLEX FROM BEEF KIDNEY MITOCHONDRIA BY PHOSPHORYLATION AND DEPHOSPHORYLATION
  Proceedings of the National Academy of Sciences, 1969