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Journal Abstract Search

166 related items for PubMed ID: 2929667

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  • 4. [The dibasic amino acid metabolic disorders].
    Shimizu H.
    Nihon Rinsho; 1992 Jul; 50(7):1555-60. PubMed ID: 1404883
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  • 14. The hyperornithinemia, hyperammonemia, homocitrullinuria syndrome: an ornithine transport defect remediable with ornithine supplements.
    Gordon BA, Gatfield DP, Haust MD.
    Clin Invest Med; 1987 Jul; 10(4):329-36. PubMed ID: 3652557
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  • 16. Ornithine loading did not prevent induced hyperammonemia in a patient with hyperornithinemia-hyperammonemia-homocitrullinuria syndrome.
    Simell O, Mackenzie S, Clow CL, Scriver CR.
    Pediatr Res; 1985 Dec; 19(12):1283-7. PubMed ID: 4080446
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  • 17. Defective ornithine metabolism in cultured skin fibroblasts from patients with the syndrome of hyperornithinemia, hyperammonemia and homocitrullinuria.
    Shih VE, Mandell R, Herzfeld A.
    Clin Chim Acta; 1982 Feb 05; 118(2-3):149-57. PubMed ID: 7055977
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  • 19. Hyperammonemia-hyperornithinemia-homocitrullinuria syndrome: neurologic, ophthalmologic, and neuropsychologic examination of six patients.
    Lemay JF, Lambert MA, Mitchell GA, Vanasse M, Valle D, Arbour JF, Dubé J, Flessas J, Laberge M, Lafleur L.
    J Pediatr; 1992 Nov 05; 121(5 Pt 1):725-30. PubMed ID: 1432421
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