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Journal Abstract Search

313 related items for PubMed ID: 904980

  • 21.
    ; . PubMed ID:
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  • 22. Lysinuric protein intolerance presenting deficiency of argininosuccinate synthetase.
    Ono N, Kishida K, Tokumoto K, Watanabe M, Shimada Y, Yoshinaga J, Fujii M.
    Intern Med; 1992 Jan; 31(1):55-9. PubMed ID: 1568044
    [Abstract] [Full Text] [Related]

  • 23. Hyperornithinemia, hyperammonemia, and homocitrullinuria. A new disorder of amino acid metabolism associated with myoclonic seizures and mental retardation.
    Shih VE, Efron ML, Moser HW.
    Am J Dis Child; 1969 Jan; 117(1):83-92. PubMed ID: 5782534
    [No Abstract] [Full Text] [Related]

  • 24.
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  • 25. [Hyperargininemia wityh arginase deficiency. A new familial metabolic disease. I. Clinical studies].
    Terheggen HG, Schwenk A, Lowenthal A, van Sande M, Colombo JP.
    Z Kinderheilkd; 1970 Jan; 107(4):298-312. PubMed ID: 5438971
    [No Abstract] [Full Text] [Related]

  • 26. Ornithinemia, hyperammonemia, and homocitrullinuria. A disease associated with mental retardation and possibly caused by defective mitochondrial transport.
    Fell V, Pollitt RJ, Sampson GA, Wright T.
    Am J Dis Child; 1974 May; 127(5):752-6. PubMed ID: 4825593
    [No Abstract] [Full Text] [Related]

  • 27. A variant form of citrullinemia.
    Matsuda I, Anakura M, Arashima S, Saito Y, Oka Y.
    J Pediatr; 1976 May; 88(5):824-6. PubMed ID: 1271146
    [No Abstract] [Full Text] [Related]

  • 28. Studies on complementation in argininosuccinate synthetase and argininosuccinate lyase deficiencies in human fibroblasts.
    Cathelineau L, Pham Dinh D, Briand P, Kamoun P.
    Hum Genet; 1981 May; 57(3):282-4. PubMed ID: 7250970
    [Abstract] [Full Text] [Related]

  • 29.
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  • 30. A case of hyperlysinemia: biochemical and clinical observations.
    Armstrong MD, Robinow M.
    Pediatrics; 1967 Apr; 39(4):546-54. PubMed ID: 6022933
    [No Abstract] [Full Text] [Related]

  • 31.
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  • 32.
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  • 33. Identification of mutations (D128G, H141L) in the liver arginase gene of patients with hyperargininemia.
    Vockley JG, Tabor DE, Kern RM, Goodman BK, Wissmann PB, Kang DS, Grody WW, Cederbaum SD.
    Hum Mutat; 1994 Apr; 4(2):150-4. PubMed ID: 7981719
    [No Abstract] [Full Text] [Related]

  • 34.
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  • 35. Hyperargininemia with arginase deficiency.
    Cederbaum SD, Shaw KN, Spector EB, Verity MA, Snodgrass PJ, Sugarman GI.
    Pediatr Res; 1979 Jul; 13(7):827-33. PubMed ID: 481955
    [No Abstract] [Full Text] [Related]

  • 36.
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  • 37. [Hyperornithinemia-hyperammonemia-homocitrullinuria (H.H.H.) syndrome].
    Oyanagi K, Nagao M.
    Ryoikibetsu Shokogun Shirizu; 1998 Jul; (18 Pt 1):185-7. PubMed ID: 9590023
    [No Abstract] [Full Text] [Related]

  • 38. [Hyperammonemia: partial carbamyl phosphate synthetase deficiency].
    Szentpéteri J, Kovács J, Földes G.
    Orv Hetil; 1982 Aug 01; 123(31):1923-6. PubMed ID: 7133689
    [No Abstract] [Full Text] [Related]

  • 39. Hyperammonemia.
    Batshaw ML.
    Curr Probl Pediatr; 1984 Nov 01; 14(11):1-69. PubMed ID: 6510017
    [Abstract] [Full Text] [Related]

  • 40.
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