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Journal Abstract Search

178 related items for PubMed ID: 4050860

  • 1. Partial pyruvate decarboxylase deficiency with profound lactic acidosis and hyperammonemia: responses to dichloroacetate and benzoate.
    McCormick K, Viscardi RM, Robinson B, Heininger J.
    Am J Med Genet; 1985 Oct; 22(2):291-9. PubMed ID: 4050860
    [Abstract] [Full Text] [Related]

  • 2. [Pyruvate dehydrogenase deficiency and cerebral malformations].
    Eirís J, Alvarez-Moreno A, Briones P, Alonso-Alonso C, Castro-Gago M.
    Rev Neurol; 1996 Oct; 24(134):1272-5. PubMed ID: 8983728
    [Abstract] [Full Text] [Related]

  • 3. Controlled clinical trial of dichloroacetate for treatment of congenital lactic acidosis in children.
    Stacpoole PW, Kerr DS, Barnes C, Bunch ST, Carney PR, Fennell EM, Felitsyn NM, Gilmore RL, Greer M, Henderson GN, Hutson AD, Neiberger RE, O'Brien RG, Perkins LA, Quisling RG, Shroads AL, Shuster JJ, Silverstein JH, Theriaque DW, Valenstein E.
    Pediatrics; 2006 May; 117(5):1519-31. PubMed ID: 16651305
    [Abstract] [Full Text] [Related]

  • 4. Therapeutic potential of dichloroacetate for pyruvate dehydrogenase complex deficiency.
    Berendzen K, Theriaque DW, Shuster J, Stacpoole PW.
    Mitochondrion; 2006 Jun; 6(3):126-35. PubMed ID: 16725381
    [Abstract] [Full Text] [Related]

  • 5. Treament of biguanide-induced lactic acidosis with dichloroacetate. 3 case histories.
    Irsigler K, Brändle J, Kaspar L, Kritz H, Lageder H, Regal H.
    Arzneimittelforschung; 1979 Jun; 29(3):555-9. PubMed ID: 582745
    [Abstract] [Full Text] [Related]

  • 6. Gas chromatographic and mass spectrometric studies on urinary organic acids in a patient with congenital lactic acidosis due to pyruvate decarboxylase deficiency.
    Chalmers RA, Lawson AM, Borud O.
    Clin Chim Acta; 1977 Jun 01; 77(2):117-24. PubMed ID: 19171
    [Abstract] [Full Text] [Related]

  • 7. Absence of pyruvate decarboxylase activity in man: a cause of congenital lactic acidosis.
    Farrell DF, Clark AF, Scott CR, Wennberg RP.
    Science; 1975 Mar 21; 187(4181):1082-4. PubMed ID: 803713
    [Abstract] [Full Text] [Related]

  • 8. Congenital lactic acidosis associated with pyruvate carboxylase deficiency. Repository identification No. GM6056.
    Oizumi J, Donnell GN, Ng WG, Mulivor RA, Greene AE, Coriell LL.
    Cytogenet Cell Genet; 1984 Mar 21; 38(1):80. PubMed ID: 6705569
    [No Abstract] [Full Text] [Related]

  • 9. Enzymologic studies and therapy of Leigh's disease associated with pyruvate decarboxylase deficiency.
    Toshima K, Kuroda Y, Hashimoto T, Ito M, Watanabe T, Miyao M, Ii K.
    Pediatr Res; 1982 Jun 21; 16(6):430-5. PubMed ID: 7099758
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  • 12. Transient improvement of congenital lactic acidosis in a male infant with pyruvate decarboxylase deficiency treated with dichloroacetate.
    Tóth PP, el-Shanti H, Eivins S, Rhead WJ, Klein JM.
    J Pediatr; 1993 Sep 21; 123(3):427-30. PubMed ID: 8355121
    [Abstract] [Full Text] [Related]

  • 13. Congenital lactic acidosis associated with pyruvate carboxylase deficiency.
    Sagy M, Barzilay Z, Barash V, Oren M, Vardi P, Cohen BE, Gutman A.
    Isr J Med Sci; 1981 Dec 21; 17(12):1159-63. PubMed ID: 6799424
    [Abstract] [Full Text] [Related]

  • 14. A case of pyruvate carboxylase deficiency with later prenatal diagnosis of an unaffected sibling.
    Tsuchiyama A, Oyanagi K, Hirano S, Tachi N, Sogawa H, Wagatsuma K, Nakao T, Tsugawa S, Kawamura Y.
    J Inherit Metab Dis; 1983 Dec 21; 6(3):85-8. PubMed ID: 6422150
    [Abstract] [Full Text] [Related]

  • 15. 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 21; 34(2):87-91. PubMed ID: 21454027
    [Abstract] [Full Text] [Related]

  • 16. Disposition of sodium benzoate in newborn infants with hyperammonemia.
    Green TP, Marchessault RP, Freese DK.
    J Pediatr; 1983 May 21; 102(5):785-90. PubMed ID: 6842341
    [Abstract] [Full Text] [Related]

  • 17. [Neonatal lactic acidosis caused by severe pyruvate carboxylase deficiency].
    Merinero Cortés B, del Valle Martínez J, Pérez-Cerdá Silvestre C, García Muñoz MJ, Cortés Coto MT, García Aparicio J, Sáez Pérez E, Ugarte Pérez M.
    An Esp Pediatr; 1988 Jul 21; 29(1):57-60. PubMed ID: 3142324
    [Abstract] [Full Text] [Related]

  • 18. Biochemical study in 28 children with lactic acidosis, in relation to Leigh's encephalomyelopathy.
    Miyabayashi S, Ito T, Narisawa K, Iinuma K, Tada K.
    Eur J Pediatr; 1985 Mar 21; 143(4):278-83. PubMed ID: 2985393
    [Abstract] [Full Text] [Related]

  • 19. Treatment of lactic acidosis with dichloroacetate.
    Stacpoole PW, Harman EM, Curry SH, Baumgartner TG, Misbin RI.
    N Engl J Med; 1983 Aug 18; 309(7):390-6. PubMed ID: 6877297
    [Abstract] [Full Text] [Related]

  • 20. Outbreak of life-threatening thiamine deficiency in infants in Israel caused by a defective soy-based formula.
    Fattal-Valevski A, Kesler A, Sela BA, Nitzan-Kaluski D, Rotstein M, Mesterman R, Toledano-Alhadef H, Stolovitch C, Hoffmann C, Globus O, Eshel G.
    Pediatrics; 2005 Feb 18; 115(2):e233-8. PubMed ID: 15687431
    [Abstract] [Full Text] [Related]

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