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Journal Abstract Search

257 related items for PubMed ID: 27070778

  • 1. Frequency and Pathophysiology of Acute Liver Failure in Ornithine Transcarbamylase Deficiency (OTCD).
    Laemmle A, Gallagher RC, Keogh A, Stricker T, Gautschi M, Nuoffer JM, Baumgartner MR, Häberle J.
    PLoS One; 2016; 11(4):e0153358. PubMed ID: 27070778
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  • 2. Significant hepatic involvement in patients with ornithine transcarbamylase deficiency.
    Gallagher RC, Lam C, Wong D, Cederbaum S, Sokol RJ.
    J Pediatr; 2014 Apr; 164(4):720-725.e6. PubMed ID: 24485820
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  • 3. Establishment of ornithine transcarbamylase deficiency-derived primary human hepatocyte with hepatic functions.
    Su S, Di Poto C, Kroemer AH, Cui W, Roy R, Liu X, Ressom HW.
    Exp Cell Res; 2019 Nov 01; 384(1):111621. PubMed ID: 31513782
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  • 7. High urgency liver transplantation in ornithine transcarbamylase deficiency presenting with acute liver failure.
    Teufel U, Weitz J, Flechtenmacher C, Prietsch V, Schmidt J, Hoffmann GF, Kölker S, Engelmann G.
    Pediatr Transplant; 2011 Sep 01; 15(6):E110-5. PubMed ID: 21884343
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  • 10. Long-term outcomes in Ornithine Transcarbamylase deficiency: a series of 90 patients.
    Brassier A, Gobin S, Arnoux JB, Valayannopoulos V, Habarou F, Kossorotoff M, Servais A, Barbier V, Dubois S, Touati G, Barouki R, Lesage F, Dupic L, Bonnefont JP, Ottolenghi C, De Lonlay P.
    Orphanet J Rare Dis; 2015 May 10; 10():58. PubMed ID: 25958381
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  • 13. Corticosteroid suppresses urea-cycle-related gene expressions in ornithine transcarbamylase deficiency.
    Imoto K, Tanaka M, Goya T, Aoyagi T, Takahashi M, Kurokawa M, Tashiro S, Kato M, Kohjima M, Ogawa Y.
    BMC Gastroenterol; 2022 Mar 28; 22(1):144. PubMed ID: 35346058
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  • 14. Ornithine transcarbamylase deficiency unmasked because of gastrointestinal bleeding.
    Trivedi M, Zafar S, Spalding MJ, Jonnalagadda S.
    J Clin Gastroenterol; 2001 Apr 28; 32(4):340-3. PubMed ID: 11276280
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  • 18. Aquaporin 9 induction in human iPSC-derived hepatocytes facilitates modeling of ornithine transcarbamylase deficiency.
    Laemmle A, Poms M, Hsu B, Borsuk M, Rüfenacht V, Robinson J, Sadowski MC, Nuoffer JM, Häberle J, Willenbring H.
    Hepatology; 2022 Sep 28; 76(3):646-659. PubMed ID: 34786702
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  • 19. Late-Onset Ornithine Transcarbamylase Deficiency Complicated with Extremely High Serum Ammonia Level: Prompt Induction of Hemodialysis as the Key to Successful Treatment.
    Yamamoto S, Yamashita S, Kakiuchi T, Kurogi K, Nishi TM, Tago M, Yamashita SI.
    Am J Case Rep; 2022 Nov 15; 23():e937658. PubMed ID: 36377209
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  • 20. Hyperammonemic encephalopathy in a child with ornithine transcarbamylase deficiency due to a novel combined heterozygous mutations.
    Gao J, Gao F, Hong F, Yu H, Jiang P.
    Am J Emerg Med; 2015 Mar 15; 33(3):474.e1-3. PubMed ID: 25227973
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