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Journal Abstract Search

100 related items for PubMed ID: 3085060

  • 1. Biochemical and histologic pathology in an infant with cross-reacting material (negative) pyruvate carboxylase deficiency.
    Wong LT, Davidson AG, Applegarth DA, Dimmick JE, Norman MG, Toone JR, Pirie G, Wong J.
    Pediatr Res; 1986 Mar; 20(3):274-9. PubMed ID: 3085060
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  • 2. 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; 17(12):1159-63. PubMed ID: 6799424
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  • 3. [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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  • 4. Secondary citrullinemia with hyperammonemia in four neonatal cases of pyruvate carboxylase deficiency.
    Coude FX, Ogier H, Marsac C, Munnich A, Charpentier C, Saudubray JM.
    Pediatrics; 1981 Dec; 68(6):914. PubMed ID: 6798542
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  • 5. 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; 45(6):1281-96. PubMed ID: 412860
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  • 6. 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
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  • 7. Pyruvate carboxylase deficiency: metabolic characteristics and new neurological aspects.
    García-Cazorla A, Rabier D, Touati G, Chadefaux-Vekemans B, Marsac C, de Lonlay P, Saudubray JM.
    Ann Neurol; 2006 Jan; 59(1):121-7. PubMed ID: 16278852
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  • 10. 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
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  • 12. Pyruvate carboxylase deficiency: a benign variant with normal development.
    Van Coster RN, Fernhoff PM, De Vivo DC.
    Pediatr Res; 1991 Jul; 30(1):1-4. PubMed ID: 1909777
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  • 15. Neonatal pyruvate carboxylase deficiency with renal tubular acidosis and cystinuria.
    Oizumi J, Shaw KN, Giudici TA, Carter M, Donnell GN, Ng WG.
    J Inherit Metab Dis; 1983 Jul; 6(3):89-94. PubMed ID: 6422151
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  • 17. Pyruvate carboxylase deficiency.
    Bartlett K, Ghneim HK, Stirk JH, Dale G, Alberti KG.
    J Inherit Metab Dis; 1984 Jul; 7 Suppl 1():74-8. PubMed ID: 6434849
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  • 18. Leigh's necrotizing encephalopathy with pyruvate carboxylase deficiency.
    Gilbert EF, Arya S, Chun R.
    Arch Pathol Lab Med; 1983 Apr; 107(4):162-6. PubMed ID: 6402999
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  • 19. Blood levels of ammonia and nitrogen scavenging amino acids in patients with inherited hyperammonemia.
    Tuchman M, Yudkoff M.
    Mol Genet Metab; 1999 Jan; 66(1):10-5. PubMed ID: 9973542
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  • 20. Treatment of pyruvate carboxylase deficiency with high doses of citrate and aspartate.
    Ahmad A, Kahler SG, Kishnani PS, Artigas-Lopez M, Pappu AS, Steiner R, Millington DS, Van Hove JL.
    Am J Med Genet; 1999 Dec 03; 87(4):331-8. PubMed ID: 10588840
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