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PUBMED FOR HANDHELDS

Journal Abstract Search


142 related items for PubMed ID: 15280615

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  • 8. A Proposed Physiopathological Pathway to Hyperammonemic Encephalopathy in a Non-Cirrhotic Patient with Fibrolamellar Hepatocellular Carcinoma without Ornithine Transcarbamylase (OTC) Mutation.
    Surjan RC, Dos Santos ES, Basseres T, Makdissi FF, Machado MA.
    Am J Case Rep; 2017 Mar 08; 18():234-241. PubMed ID: 28270654
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  • 9. Adult-onset ornithine transcarbamylase (OTC) deficiency unmasked by the Atkins' diet.
    Ben-Ari Z, Dalal A, Morry A, Pitlik S, Zinger P, Cohen J, Fattal I, Galili-Mosberg R, Tessler D, Baruch RG, Nuoffer JM, Largiader CR, Mandel H.
    J Hepatol; 2010 Feb 08; 52(2):292-5. PubMed ID: 20031247
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  • 14. [Hyperammonemia type II as an example of urea cycle disorder].
    Hawrot-Kawecka AM, Kawecki GP, Duława J.
    Wiad Lek; 2006 Feb 08; 59(7-8):512-5. PubMed ID: 17209350
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  • 15. Ornithine transcarbamylase deficiency: adult onset of severe symptoms.
    Gilchrist JM, Coleman RA.
    Ann Intern Med; 1987 Apr 08; 106(4):556-8. PubMed ID: 3826955
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  • 16. Corticosteroid-induced hyperammonaemic encephalopathy in a woman with late-onset ornithine transcarbamylase deficiency.
    McCormick BJ, Ritchie LV, Porter IE.
    BMJ Case Rep; 2024 May 02; 17(5):. PubMed ID: 38697679
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  • 19. Complete recovery from acute encephalopathy of late-onset ornithine transcarbamylase deficiency in a 3-year-old boy.
    Mak CM, Siu TS, Lam CW, Chan GC, Poon GW, Wong KY, Low LC, Tang NL, Li SK, Lau KY, Kwong NS, Tam S.
    J Inherit Metab Dis; 2007 Nov 02; 30(6):981. PubMed ID: 17922216
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  • 20. Hyperammonemic coma in an ornithine transcarbamylase mutation carrier following antepartum corticosteroids.
    Lipskind S, Loanzon S, Simi E, Ouyang DW.
    J Perinatol; 2011 Oct 02; 31(10):682-4. PubMed ID: 21956151
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