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Journal Abstract Search

216 related items for PubMed ID: 7797025

  • 1. Hyperammonemic coma due to parenteral nutrition in a woman with heterozygous ornithine transcarbamylase deficiency.
    Felig DM, Brusilow SW, Boyer JL.
    Gastroenterology; 1995 Jul; 109(1):282-4. PubMed ID: 7797025
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  • 2.
    Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Amemiya A, Lichter-Konecki U, Caldovic L, Morizono H, Simpson K, Ah Mew N, MacLeod E.
    ; 1993 Jul. PubMed ID: 24006547
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  • 3. Ornithine transcarbamylase deficiency unmasked because of gastrointestinal bleeding.
    Trivedi M, Zafar S, Spalding MJ, Jonnalagadda S.
    J Clin Gastroenterol; 2001 Apr; 32(4):340-3. PubMed ID: 11276280
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  • 4. Risk of serious illness in heterozygotes for ornithine transcarbamylase deficiency.
    Batshaw ML, Msall M, Beaudet AL, Trojak J.
    J Pediatr; 1986 Feb; 108(2):236-41. PubMed ID: 3944708
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  • 5. Hyperammonemia in a Woman with Late-onset Ornithine Transcarbamylase Deficiency.
    Koya Y, Shibata M, Senju M, Honma Y, Hiura M, Ishii M, Matsumoto S, Harada M.
    Intern Med; 2019 Apr 01; 58(7):937-942. PubMed ID: 30449781
    [Abstract] [Full Text] [Related]

  • 6. Heterozygote ornithine transcarbamylase deficiency presenting as symptomatic hyperammonemia during initiation of valproate therapy.
    Honeycutt D, Callahan K, Rutledge L, Evans B.
    Neurology; 1992 Mar 01; 42(3 Pt 1):666-8. PubMed ID: 1549234
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  • 7. Ornithine transcarbamylase deficiency in females: an often overlooked cause of treatable encephalopathy.
    Pridmore CL, Clarke JT, Blaser S.
    J Child Neurol; 1995 Sep 01; 10(5):369-74. PubMed ID: 7499756
    [Abstract] [Full Text] [Related]

  • 8. Fatal coma in a young adult due to late-onset urea cycle deficiency presenting with a prolonged seizure: a case report.
    Alameri M, Shakra M, Alsaadi T.
    J Med Case Rep; 2015 Nov 23; 9():267. PubMed ID: 26593089
    [Abstract] [Full Text] [Related]

  • 9. Fatal clinical course of ornithine transcarbamylase deficiency in an adult heterozygous female patient.
    Heringlake S, Böker K, Manns M.
    Digestion; 1997 Nov 23; 58(1):83-6. PubMed ID: 9018015
    [Abstract] [Full Text] [Related]

  • 10. Partial ornithine transcarbamylase deficiency associated with recurrent hyperammonemia, lethargy and depressed sensorium.
    Oizumi J, Ng WG, Koch R, Shaw KN, Sweetman L, Velazquez A, Donnell GN.
    Clin Genet; 1984 Jun 23; 25(6):538-42. PubMed ID: 6733950
    [Abstract] [Full Text] [Related]

  • 11. Curative Treatment of Ornithine Transcarbamylase Deficiency With a Liver Transplant: A Case Report.
    Shamsaeefar A, Nikeghbalian S, Dehghani SM, Kazemi K, Motazedian N, Geramizadeh B, Malekhosseini SA.
    Exp Clin Transplant; 2019 Feb 23; 17(1):119-120. PubMed ID: 27447480
    [Abstract] [Full Text] [Related]

  • 12. [Fulminant coma: think hyperammonemia and urea cycle disorders].
    Augris C, Jouvet P, Benabdelmalek F, Vauquelin P, Caramella JP.
    Ann Fr Anesth Reanim; 2002 Dec 23; 21(10):820-3. PubMed ID: 12534125
    [Abstract] [Full Text] [Related]

  • 13. Late-onset presentation of ornithine transcarbamylase deficiency in a young woman with hyperammonemic coma.
    Gaspari R, Arcangeli A, Mensi S, Wismayer DS, Tartaglione T, Antuzzi D, Conti G, Proietti R.
    Ann Emerg Med; 2003 Jan 23; 41(1):104-9. PubMed ID: 12514690
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  • 19. Hyperammoniemic coma in an adolescent girl: an unusual case of ornithine transcarbamylase deficiency.
    Perini M, Zarcone D, Corbetta C.
    Ital J Neurol Sci; 1993 Sep 23; 14(6):461-4. PubMed ID: 8282523
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