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Journal Abstract Search

396 related items for PubMed ID: 954343

  • 1. Congenital hyperammonemic syndromes.
    Shih VE.
    Clin Perinatol; 1976 Mar; 3(1):3-14. PubMed ID: 954343
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  • 3. Urea cycle enzymopathies.
    Walser M.
    Semin Liver Dis; 1982 Nov; 2(4):329-39. PubMed ID: 6763345
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  • 4. [Molecular basis of urea cycle disorders].
    Matsuda I, Matsuura T, Hoshide R, Uchino T, Matsubasa T.
    Nihon Rinsho; 1993 Feb; 51(2):520-4. PubMed ID: 8464164
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  • 8. Disorders of the urea cycle.
    Brusilow SW.
    Hosp Pract (Off Ed); 1985 Oct 15; 20(10):65-72. PubMed ID: 3930543
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  • 9. Plasma alpha-ketoglutarate in urea cycle enzymopathies and its role as a harbinger of hyperammonemic coma.
    Batshaw ML, Walser M, Brusilow SW.
    Pediatr Res; 1980 Dec 15; 14(12):1316-9. PubMed ID: 7208146
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  • 10. Treatment of inborn errors of urea synthesis: activation of alternative pathways of waste nitrogen synthesis and excretion.
    Batshaw ML, Brusilow S, Waber L, Blom W, Brubakk AM, Burton BK, Cann HM, Kerr D, Mamunes P, Matalon R, Myerberg D, Schafer IA.
    N Engl J Med; 1982 Jun 10; 306(23):1387-92. PubMed ID: 7078580
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  • 11. Double deficiencies of urea cycle enzymes in human liver.
    Raijman L.
    Biochem Med; 1979 Apr 10; 21(2):226-33. PubMed ID: 465019
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  • 19. Genetic approach to prenatal diagnosis in urea cycle defects.
    Häberle J, Koch HG.
    Prenat Diagn; 2004 May 10; 24(5):378-83. PubMed ID: 15164414
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