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Journal Abstract Search

169 related items for PubMed ID: 6790846

  • 1. Lactic acidosis due to pyruvate carboxylase deficiency.
    Haworth JC, Robinson BH, Perry TL.
    J Inherit Metab Dis; 1981; 4(2):57-8. PubMed ID: 6790846
    [Abstract] [Full Text] [Related]

  • 2. [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; 29(1):57-60. PubMed ID: 3142324
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  • 3. Neonatal congenital lactic acidosis with pyruvate carboxylase deficiency in two siblings.
    Saudubray JM, Marsac C, Cathelineau CL, Besson Leaud M, Leroux JP.
    Acta Paediatr Scand; 1976 Nov; 65(6):717-24. PubMed ID: 826106
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  • 4. [Differential diagnosis of the symptom of lactic acidosis in childhood].
    Koepp P.
    Monatsschr Kinderheilkd; 1984 May; 132(5):264-7. PubMed ID: 6087128
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  • 5. 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
    [Abstract] [Full Text] [Related]

  • 6. [Enzymopathic congenital hyperlactacidemia].
    Leroux JP, Marsac C, Saudubray JM.
    Ann Biol Clin (Paris); 1976 Aug; 34(2):151-9. PubMed ID: 184725
    [Abstract] [Full Text] [Related]

  • 7. Pyruvate carboxylase deficiency and lactic acidosis in a retarded child without Leigh's disease.
    Atkin BM, Buist NR, Utter MF, Leiter AB, Banker BQ.
    Pediatr Res; 1979 Feb; 13(2):109-16. PubMed ID: 219411
    [Abstract] [Full Text] [Related]

  • 8. 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; 58(4):564-72. PubMed ID: 184426
    [Abstract] [Full Text] [Related]

  • 9. Pyruvate-carboxylase deficiency with urea cycle impairment.
    Greter J, Gustafsson J, Holme E.
    Acta Paediatr Scand; 1985 Nov; 74(6):982-6. PubMed ID: 3937431
    [Abstract] [Full Text] [Related]

  • 10. Problems in the congenital lactic acidoses.
    Leonard JV.
    Ciba Found Symp; 1982 Nov; 87():340-56. PubMed ID: 6280937
    [Abstract] [Full Text] [Related]

  • 11. Congenital lactic acidosis due to pyruvate carboxylase deficiency: absence of an inhibitor of TPP-ATP phosphoryl transferase.
    Tada K, Takada G, Omura K, Itokawa Y.
    Eur J Pediatr; 1978 Jan 17; 127(2):141-7. PubMed ID: 203466
    [Abstract] [Full Text] [Related]

  • 12. Lactic acidaemia.
    Robinson BH, Sherwood WG.
    J Inherit Metab Dis; 1984 Jan 17; 7 Suppl 1():69-73. PubMed ID: 6434848
    [Abstract] [Full Text] [Related]

  • 13. Hyperalaninemia hyperpyruvicemia and lactic acidosis due to pyruvate carboxylase deficiency of the liver; treatment with thiamine and lipoic acid.
    Maesaka H, Komiya K, Misugi K, Tada K.
    Eur J Pediatr; 1976 May 04; 122(2):159-68. PubMed ID: 817914
    [Abstract] [Full Text] [Related]

  • 14. Fatal lactic acidosis in a newborn attributable to a congenital defect of pyruvate dehydrogenase.
    Strömme JH, Borud O, Moe PJ.
    Pediatr Res; 1976 Jan 04; 10(1):62-6. PubMed ID: 813176
    [Abstract] [Full Text] [Related]

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  • 18. The clinical and biochemical implications of pyruvate carboxylase deficiency.
    DeVivo DC, Haymond MW, Leckie MP, Bussman YL, McDougal DB, Pagliara AS.
    J Clin Endocrinol Metab; 1977 Dec 04; 45(6):1281-96. PubMed ID: 412860
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  • 20. Mitochondrial pyruvate metabolism in liver and kidney during acidosis.
    Oliver FJ, Salto R, Sola MM, Vargas AM.
    Cell Biochem Funct; 1994 Dec 04; 12(4):229-35. PubMed ID: 7834811
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