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PUBMED FOR HANDHELDS

Journal Abstract Search


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
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  • 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
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  • 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
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  • 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
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  • 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
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  • 31. The metabolic effects of dichloroacetate.
    Crabb DW, Yount EA, Harris RA.
    Metabolism; 1981 Oct 31; 30(10):1024-39. PubMed ID: 7024720
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  • 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
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  • 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
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  • 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
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  • 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
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  • 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
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  • 39. Amelioration of lactic acidosis with dichloroacetate during liver transplantation in humans.
    Shangraw RE, Winter R, Hromco J, Robinson ST, Gallaher EJ.
    Anesthesiology; 1994 Nov 31; 81(5):1127-38. PubMed ID: 7978471
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  • 40. Studies of urinary organic acid profiles of a patient with dihydrolipoyl dehydrogenase deficiency.
    Kuhara T, Shinka T, Inoue Y, Matsumoto M, Yoshino M, Sakaguchi Y, Matsumoto I.
    Clin Chim Acta; 1983 Sep 30; 133(2):133-40. PubMed ID: 6688766
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