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Journal Abstract Search

356 related items for PubMed ID: 8581654

  • 1. [Urea cycle disorders].
    Tazawa Y.
    Ryoikibetsu Shokogun Shirizu; 1995; (8):367-9. PubMed ID: 8581654
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  • 3. Congenital hyperammonemic syndromes.
    Shih VE.
    Clin Perinatol; 1976 Mar; 3(1):3-14. PubMed ID: 954343
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  • 7. [Hereditary diseases related to a disorder of the enzymatic activity of the urea formation cycle].
    Kazanskaia NS, Alekseenko LP.
    Vopr Med Khim; 1976 Mar; 22(4):435-43. PubMed ID: 800301
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  • 14. 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; 14(12):1316-9. PubMed ID: 7208146
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  • 15. Editorial: Ammonia disposal in Reye's syndrome.
    Smith AL.
    N Engl J Med; 1976 Apr 15; 294(16):897-8. PubMed ID: 1250317
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  • 16. [Neonatal hyperammonemia].
    Jaeken J, Devlieger H, Evens M, Casaer P, Eggermont E.
    Tijdschr Kindergeneeskd; 1983 Jun 15; 51(3):101-4. PubMed ID: 6636106
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  • 20. Sodium benzoate and arginine: alternative pathway therapy in inborn errors of urea synthesis.
    Batshaw ML.
    Prog Clin Biol Res; 1983 Jun 15; 127():69-83. PubMed ID: 6889404
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