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169 related items for PubMed ID: 8652022
21. Lipoamide dehydrogenase deficiency due to a novel mutation in the interface domain. Shany E, Saada A, Landau D, Shaag A, Hershkovitz E, Elpeleg ON. Biochem Biophys Res Commun; 1999 Aug 19; 262(1):163-6. PubMed ID: 10448086 [Abstract] [Full Text] [Related]
24. Beneficial effect of pyruvate therapy on Leigh syndrome due to a novel mutation in PDH E1α gene. Koga Y, Povalko N, Katayama K, Kakimoto N, Matsuishi T, Naito E, Tanaka M. Brain Dev; 2012 Feb 19; 34(2):87-91. PubMed ID: 21454027 [Abstract] [Full Text] [Related]
28. Immunoextraction of lipoamide dehydrogenase from cultured skin fibroblasts in patients with combined alpha-ketoacid dehydrogenase deficiency. Otulakowski G, Nyhan W, Sweetman L, Robinson BH. Clin Chim Acta; 1985 Oct 31; 152(1-2):27-36. PubMed ID: 2414042 [Abstract] [Full Text] [Related]
29. Clinical and radiologic improvements in mitochondrial encephalomyelopathy following sodium dichloroacetate therapy. Kimura S, Ohtuki N, Nezu A, Tanaka M, Takeshita S. Brain Dev; 1997 Dec 31; 19(8):535-40. PubMed ID: 9440797 [Abstract] [Full Text] [Related]
30. Molecular analysis of abnormal pyruvate dehydrogenase in a patient with thiamine-responsive congenital lactic acidemia. Naito E, Ito M, Takeda E, Yokota I, Yoshijima S, Kuroda Y. Pediatr Res; 1994 Sep 31; 36(3):340-6. PubMed ID: 7808831 [Abstract] [Full Text] [Related]
31. The metabolic effects of dichloroacetate. Crabb DW, Yount EA, Harris RA. Metabolism; 1981 Oct 31; 30(10):1024-39. PubMed ID: 7024720 [No Abstract] [Full Text] [Related]
32. Congenital lactic acidosis. Kuroda Y, Naito E, Takeda E, Yokota I, Miyao M. Enzyme; 1987 Oct 31; 38(1-4):108-14. PubMed ID: 3440441 [Abstract] [Full Text] [Related]
33. Inhibition of glycine oxidation by pyruvate, alpha-ketoglutarate, and branched-chain alpha-keto acids in rat liver mitochondria: presence of interaction between the glycine cleavage system and alpha-keto acid dehydrogenase complexes. Kochi H, Seino H, Ono K. Arch Biochem Biophys; 1986 Sep 31; 249(2):263-72. PubMed ID: 3753002 [Abstract] [Full Text] [Related]
34. A new case of pyruvate dehydrogenase deficiency due to a novel mutation in the PDX1 gene. Dey R, Mine M, Desguerre I, Slama A, Van Den Berghe L, Brivet M, Aral B, Marsac C. Ann Neurol; 2003 Feb 31; 53(2):273-7. PubMed ID: 12557299 [Abstract] [Full Text] [Related]
35. Dichloroacetate therapy in Leigh syndrome with a mitochondrial T8993C mutation. Fujii T, Ito M, Miyajima T, Okuno T. Pediatr Neurol; 2002 Jul 31; 27(1):58-61. PubMed ID: 12160976 [Abstract] [Full Text] [Related]
36. Lactic acidosis in three sibs due to defects in both pyruvate dehydrogenase and alpha-ketoglutarate dehydrogenase complexes. Haworth JC, Perry TL, Blass JP, Hansen S, Urquhart N. Pediatrics; 1976 Oct 31; 58(4):564-72. PubMed ID: 184426 [Abstract] [Full Text] [Related]