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Journal Abstract Search

160 related items for PubMed ID: 2974563

  • 21. Use of citrulline as a diagnostic marker in the prospective treatment of urea cycle disorders.
    Batshaw ML, Berry GT.
    J Pediatr; 1991 Jun; 118(6):914-7. PubMed ID: 2040929
    [No Abstract] [Full Text] [Related]

  • 22. Hyperammonemia: the silent killer.
    Miga DE, Roth KS.
    South Med J; 1993 Jul; 86(7):742-7. PubMed ID: 8322080
    [Abstract] [Full Text] [Related]

  • 23. Molecular genetic research into carbamoyl-phosphate synthase I: molecular defects and linkage markers.
    Summar ML.
    J Inherit Metab Dis; 1998 Jul; 21 Suppl 1():30-9. PubMed ID: 9686343
    [Abstract] [Full Text] [Related]

  • 24. Treatment of episodic hyperammonemia in children with inborn errors of urea synthesis.
    Brusilow SW, Danney M, Waber LJ, Batshaw M, Burton B, Levitsky L, Roth K, McKeethren C, Ward J.
    N Engl J Med; 1984 Jun 21; 310(25):1630-4. PubMed ID: 6427608
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  • 27. Congenital hyperammonemic syndromes.
    Shih VE.
    Clin Perinatol; 1976 Mar 21; 3(1):3-14. PubMed ID: 954343
    [Abstract] [Full Text] [Related]

  • 28. A case of carbamylphosphate synthetase-I deficiency associated with secondary carnitine deficiency--L-carnitine treatment of CPS-I deficiency.
    Mori T, Tsuchiyama A, Nagai K, Nagao M, Oyanagi K, Tsugawa S.
    Eur J Pediatr; 1990 Jan 21; 149(4):272-4. PubMed ID: 2303075
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  • 30. 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 21; 29(1):181-5. PubMed ID: 9862865
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  • 32. Organic acids and Reye's syndrome.
    Applegarth DA, MacLeod PM, Toone JR, Kirby LT, MacLean JR, Mamer OA, Montgomery JA.
    Lancet; 1979 May 26; 1(8126):1147. PubMed ID: 86873
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  • 35. [Pharmacokinetics of biological tags in a case of acute valpromide self poisoning].
    Commandeur D, Danguy Des Deserts M, Giacardi C, Eyrieux S, Ould-Ahmed M, Drouillard I.
    Ann Biol Clin (Paris); 2010 May 26; 68(2):234-8. PubMed ID: 20348051
    [Abstract] [Full Text] [Related]

  • 36. Arginine, an indispensable amino acid for patients with inborn errors of urea synthesis.
    Brusilow SW.
    J Clin Invest; 1984 Dec 26; 74(6):2144-8. PubMed ID: 6511918
    [Abstract] [Full Text] [Related]

  • 37. Prospective versus clinical diagnosis and therapy of acute neonatal hyperammonaemia in two sisters with carbamyl phosphate synthetase deficiency.
    Tuchman M, Mauer SM, Holzknecht RA, Summar ML, Vnencak-Jones CL.
    J Inherit Metab Dis; 1992 Dec 26; 15(2):269-77. PubMed ID: 1356172
    [Abstract] [Full Text] [Related]

  • 38. Hyperammonemia (ornithinemia) presenting as a unilateral cerebral mass lesion.
    Amacher AL, Bolton RJ, Gatfield PD.
    Surg Neurol; 1976 Sep 26; (3):159-62. PubMed ID: 959986
    [No Abstract] [Full Text] [Related]

  • 39. Fatal hyperammonemia and carbamoyl phosphate synthetase 1 (CPS1) deficiency following high-dose chemotherapy and autologous hematopoietic stem cell transplantation.
    Laemmle A, Hahn D, Hu L, Rüfenacht V, Gautschi M, Leibundgut K, Nuoffer JM, Häberle J.
    Mol Genet Metab; 2015 Mar 26; 114(3):438-44. PubMed ID: 25639153
    [Abstract] [Full Text] [Related]

  • 40. Valproate-induced hyperammonemic encephalopathy.
    Segura-Bruna N, Rodriguez-Campello A, Puente V, Roquer J.
    Acta Neurol Scand; 2006 Jul 26; 114(1):1-7. PubMed ID: 16774619
    [Abstract] [Full Text] [Related]

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