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PUBMED FOR HANDHELDS

Journal Abstract Search

201 related items for PubMed ID: 7355003

  • 21. Inborn errors of urea synthesis.
    Batshaw ML.
    Ann Neurol; 1994 Feb; 35(2):133-41. PubMed ID: 7906500
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  • 32. 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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  • 35. Arginine deficiency syndrome. Its occurrence in carbamyl phosphate synthetase deficiency.
    Kline JJ, Hug G, Schubert WK, Berry H.
    Am J Dis Child; 1981 May; 135(5):437-42. PubMed ID: 7234771
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  • 37. 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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  • 38. Diagnosis of urea cycle disorders.
    Bachmann C.
    Enzyme; 1987 Jan; 38(1-4):233-41. PubMed ID: 3440447
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  • 39. [Inherited hyperammonemia].
    Bik-Multanowski M.
    Przegl Lek; 1998 Jan; 55(6):337-41. PubMed ID: 9857711
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  • 40. Mice deficient in the urea-cycle enzyme, carbamoyl phosphate synthetase I, die during the early neonatal period from hyperammonemia.
    Schofield JP, Cox TM, Caskey CT, Wakamiya M.
    Hepatology; 1999 Jan; 29(1):181-5. PubMed ID: 9862865
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