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Journal Abstract Search

178 related items for PubMed ID: 4050860

  • 21. Magnetic resonance spectroscopic investigation of mitochondrial fuel metabolism and energetics in cultured human fibroblasts: effects of pyruvate dehydrogenase complex deficiency and dichloroacetate.
    Simpson NE, Han Z, Berendzen KM, Sweeney CA, Oca-Cossio JA, Constantinidis I, Stacpoole PW.
    Mol Genet Metab; 2006; 89(1-2):97-105. PubMed ID: 16765624
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  • 22. [Carnitine levels in muscle in mice with hyperammonemia: effect of treatment with sodium benzoate].
    Michalak A, Qureshi IA.
    Can J Physiol Pharmacol; 1993 Jul; 71(7):439-46. PubMed ID: 8242478
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  • 23. Urinary organic acids in a case of congenital lactic acidosis due to pyruvate decarboxylase deficiency.
    Chalmers RA, Lawson AM, Borud O.
    J Inherit Metab Dis; 1978 Jul; 1(1):15-6. PubMed ID: 117229
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  • 24. [Congenital lactic acidemia].
    Narisawa K, Miyabayashi S, Tada K.
    Rinsho Shinkeigaku; 1983 Dec; 23(12):1113-5. PubMed ID: 6329573
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  • 25. Detection of pyruvate metabolism disorders by culture of skin fibroblasts with dichloroacetate.
    Naito E, Kuroda Y, Takeda E, Yokota I, Kobashi H, Miyao M.
    Pediatr Res; 1988 Jun; 23(6):561-4. PubMed ID: 2839811
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  • 26. Fatal lactic acidosis in a newborn attributable to a congenital defect of pyruvate dehydrogenase.
    Strömme JH, Borud O, Moe PJ.
    Pediatr Res; 1976 Jan; 10(1):62-6. PubMed ID: 813176
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  • 28. [Acute encephalopathy due to thiamine deficiency with hyperammonemia in a chronic hemodialysis patient: a case report].
    Ookawara S, Suzuki M, Saitou M.
    Nihon Jinzo Gakkai Shi; 2003 Jan; 45(4):393-7. PubMed ID: 12806978
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  • 29. The genetic heterogeneity of lactic acidosis: occurrence of recognizable inborn errors of metabolism in pediatric population with lactic acidosis.
    Robinson BH, Taylor J, Sherwood WG.
    Pediatr Res; 1980 Aug; 14(8):956-62. PubMed ID: 6775276
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  • 37. Treatment of chronic congenital lactic acidosis by oral administration of dichloroacetate.
    Kuroda Y, Ito M, Toshima K, Takeda E, Naito E, Hwang TJ, Hashimoto T, Miyao M, Masuda M, Yamashita K.
    J Inherit Metab Dis; 1986 Aug; 9(3):244-52. PubMed ID: 3099068
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  • 38. Deficiency of pyruvate dehydrogenase complex in tissues of an eight month old infant.
    Hansikova H, Zeman J, Klement P, Technikova-Dobrova Z, Houstkova H, Houstek J, Papa S.
    Biochem Mol Biol Int; 1993 Dec; 31(6):1157-66. PubMed ID: 8193600
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