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Journal Abstract Search

215 related items for PubMed ID: 12534125

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

  • 2. 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
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  • 3. [Hyperammonemia type II as an example of urea cycle disorder].
    Hawrot-Kawecka AM, Kawecki GP, Duława J.
    Wiad Lek; 2006 Nov 23; 59(7-8):512-5. PubMed ID: 17209350
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  • 4. 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
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  • 5. Hyperammonemic coma in a patient with late-onset OTC deficiency.
    D'Onofrio V, Poma F, Enea A, Santarelli F, Lovera C, Spada M.
    Pediatr Med Chir; 2014 Jun 30; 36(3):9. PubMed ID: 25573644
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  • 6. Coma query cause.
    Wood GE, McNicholas J.
    BMJ Case Rep; 2015 May 06; 2015():. PubMed ID: 25948840
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  • 7. Fatal hyperammonaemia due to late-onset ornithine transcarbamylase deficiency.
    Bijvoet GP, van der Sijs-Bos CJ, Wielders JP, Groot OA.
    Neth J Med; 2016 Jan 06; 74(1):36-9. PubMed ID: 26819360
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  • 8. Prenatal treatment of ornithine transcarbamylase deficiency.
    Wilnai Y, Blumenfeld YJ, Cusmano K, Hintz SR, Alcorn D, Benitz WE, Berquist WE, Bernstein JA, Castillo RO, Concepcion W, Cowan TM, Cox KL, Lyell DJ, Esquivel CO, Homeyer M, Hudgins L, Hurwitz M, Palma JP, Schelley S, Akula VP, Summar ML, Enns GM.
    Mol Genet Metab; 2018 Mar 06; 123(3):297-300. PubMed ID: 29396029
    [Abstract] [Full Text] [Related]

  • 9. Clinical findings of patients with hyperammonemia affected by urea cycle disorders with hepatic encephalopathy.
    Lopes FF, Sitta A, de Moura Coelho D, Ribas GS, Faverzani JL, Dos Reis BG, Wajner M, Vargas CR.
    Int J Dev Neurosci; 2022 Dec 06; 82(8):772-788. PubMed ID: 36129623
    [Abstract] [Full Text] [Related]

  • 10. Late-onset of ornithine transcarbamylase deficiency: A rare medical examiner case.
    Gitto L, Fuller CE, Calleo VJ, Tawil M, Thach R, Revercomb C.
    J Forensic Sci; 2022 Mar 06; 67(2):813-819. PubMed ID: 34726276
    [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 06; 17(1):119-120. PubMed ID: 27447480
    [Abstract] [Full Text] [Related]

  • 12. Hyperammonemic coma in an ornithine transcarbamylase mutation carrier following antepartum corticosteroids.
    Lipskind S, Loanzon S, Simi E, Ouyang DW.
    J Perinatol; 2011 Oct 06; 31(10):682-4. PubMed ID: 21956151
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  • 18. A rare cause of postpartum coma: isolated hyperammonemia due to urea cycle disorder.
    Açıkalın A, Dişel NR, Direk EÇ, Ilgınel MT, Sebe A, Bıçakçı Ş.
    Am J Emerg Med; 2016 Jul 06; 34(7):1324.e3-4. PubMed ID: 26776297
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  • 19. The urea cycle disorders.
    Helman G, Pacheco-Colón I, Gropman AL.
    Semin Neurol; 2014 Jul 06; 34(3):341-9. PubMed ID: 25192511
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