Friedreich'S Ataxia: I. Normal pyruvate dehydrogenase complex activity in platelets
Author:
Publisher
Wiley
Subject
Clinical Neurology,Neurology
Reference15 articles.
1. Pyruvate Metabolism in Friedreich's Ataxia
2. A defect in pyruvate decarboxylase in a child with an intermittent movement disorder
3. Rapid diagnosis of pyruvate and ketoglutarate dehydrogenase deficiencies in platelet-enriched preparations from blood
4. Low Activities of the Pyruvate and Oxoglutarate Dehydrogenase Complexes in Five Patients with Friedreich's Ataxia
5. An inherited defect affecting the tricarboxylic acid cycle in a patient with congenital lactic acidosis
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1. Problems in the Congenital Lactic Acidoses;Ciba Foundation Symposium 87 - Metabolic Acidosis;2008-05-30
2. Production of Recombinant Mammalian Holo-E2 and E3 and Reconstitution of Functional Branched-Chain α-Keto Acid Dehydrogenase Complex with Recombinant E1;Branched-Chain Amino Acids, Part B;2000
3. Muscle biochemistry in thiamin-responsive anaemia;Journal of Inherited Metabolic Disease;1997-07
4. Brain pyruvate oxidation in experimental thiamin-deficiency encephalopathy;Clinica Chimica Acta;1996-11
5. Immunoreactive Levels of α-ketoglutarate Dehydrogenase Subunits in Friedreich's Ataxia and Spinocerebellar Ataxia Type 1;Neurodegeneration;1996-03
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