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Journal Abstract Search

173 related items for PubMed ID: 206210

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  • 4. Severe neonatal deficiency of carbamylphosphate synthetase.
    Lambotte C, Adam A, Van Der Hofstadt J, Dodinval-Versie J, Gielen J.
    Acta Paediatr Belg; 1977; 30(3):151-5. PubMed ID: 204150
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  • 8. Kinetic abnormalities of carbamyl phosphate synthetase-I in a case of congenital hyperammonaemia.
    Qureshi IA, Letarte J, Ouellet R, Lemieux B, Cathelineau L.
    J Inherit Metab Dis; 1986; 9(3):253-60. PubMed ID: 3099069
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  • 16. Transient hyperammonemias in infants with and without organic acidemia.
    Nyhan WL, Rubio V, Jordá A, Grisolia S, Gutierez F, Canosa C.
    Adv Exp Med Biol; 1982; 153():331-8. PubMed ID: 7164908
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  • 17. Arginine, an indispensable amino acid for patients with inborn errors of urea synthesis.
    Brusilow SW.
    J Clin Invest; 1984 Dec; 74(6):2144-8. PubMed ID: 6511918
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  • 18. A lethal neonatal variant of carbamoyl-phosphate synthetase deficiency in combination with an intermediate activity of L-ornithine: 2-oxoglutarate amino-transferase.
    van der Heiden C, Beemer FA, van Dijk HA, Desplanque J, Gerards LJ.
    Clin Genet; 1983 May; 23(5):363-8. PubMed ID: 6851228
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  • 19. Liver ultrastructure in mitochondrial urea cycle enzyme deficiencies and comparison with Reye's syndrome.
    Latham PS, LaBrecque DR, McReynolds JW, Klatskin G.
    Hepatology; 1984 May; 4(3):404-7. PubMed ID: 6724509
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