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Journal Abstract Search

313 related items for PubMed ID: 11276280

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  • 24. 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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  • 27. 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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  • 29. 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 23; 52(2):292-5. PubMed ID: 20031247
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  • 30. Long-term treatment of girls with ornithine transcarbamylase deficiency.
    Maestri NE, Brusilow SW, Clissold DB, Bassett SS.
    N Engl J Med; 1996 Sep 19; 335(12):855-9. PubMed ID: 8778603
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  • 31. Ornithine transcarbamylase (OTC) in white blood cells.
    Nagata N, Akaboshi I, Yamamoto J, Matsuda I, Ohtsuka H, Katsuki T.
    Pediatr Res; 1980 Dec 19; 14(12):1370-3. PubMed ID: 7208155
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  • 34. Hyperammonemia in a patient with late-onset ornithine carbamoyltransferase deficiency.
    Choi DE, Lee KW, Shin YT, Na KR.
    J Korean Med Sci; 2012 May 19; 27(5):556-9. PubMed ID: 22563224
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  • 35. 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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  • 36. Liver ultrastructure in mitochondrial urea cycle enzyme deficiencies and comparison with Reye's syndrome.
    Latham PS, LaBrecque DR, McReynolds JW, Klatskin G.
    Hepatology; 1984 Nov 15; 4(3):404-7. PubMed ID: 6724509
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  • 37. [Consensus on diagnosis and treatment of ornithine trans-carbamylase deficiency].
    Division of Genetics and Metabolism, Child Diseases and Health Care Branch, Chinese Association for Maternal and Child Health.
    Zhejiang Da Xue Xue Bao Yi Xue Ban; 2020 Oct 25; 49(5):539-547. PubMed ID: 33210478
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  • 38. Transiently reduced activity of carbamyl phosphate synthetase and ornithine transcarbamylase in liver of children with Reye's syndrome.
    Brown T, Hug G, Lansky L, Bove K, Scheve A, Ryan M, Brown H, Schubert WK, Partin JC, Lloyd-Still J.
    N Engl J Med; 1976 Apr 15; 294(16):861-7. PubMed ID: 175276
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  • 39. The phenotypic and mutational spectrum of Thai female patients with ornithine transcarbamylase deficiency.
    Chongsrisawat V, Damrongphol P, Ittiwut C, Ittiwut R, Suphapeetiporn K, Shotelersuk V.
    Gene; 2018 Dec 30; 679():377-381. PubMed ID: 30223008
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