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PUBMED FOR HANDHELDS

Journal Abstract Search


307 related items for PubMed ID: 21956151

  • 1. Hyperammonemic coma in an ornithine transcarbamylase mutation carrier following antepartum corticosteroids.
    Lipskind S, Loanzon S, Simi E, Ouyang DW.
    J Perinatol; 2011 Oct; 31(10):682-4. PubMed ID: 21956151
    [Abstract] [Full Text] [Related]

  • 2. Management of ornithine transcarbamylase deficiency in pregnancy.
    Mendez-Figueroa H, Lamance K, Sutton VR, Aagaard-Tillery K, Van den Veyver I.
    Am J Perinatol; 2010 Nov; 27(10):775-84. PubMed ID: 20458665
    [Abstract] [Full Text] [Related]

  • 3. 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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  • 4. [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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  • 5. 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 23; 33(3):474.e1-3. PubMed ID: 25227973
    [Abstract] [Full Text] [Related]

  • 6. Ornithine transcarbamylase deficiency in pregnancy.
    Cordero DR, Baker J, Dorinzi D, Toffle R.
    J Inherit Metab Dis; 2005 Mar 23; 28(2):237-40. PubMed ID: 15877212
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  • 8. 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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  • 10. Fatal initial adult-onset presentation of urea cycle defect.
    Lien J, Nyhan WL, Barshop BA.
    Arch Neurol; 2007 Dec 01; 64(12):1777-9. PubMed ID: 18071043
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  • 12. 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 01; 52(2):292-5. PubMed ID: 20031247
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  • 13. Fatal hyperammonemic coma caused by ornithine transcarbamylase deficiency in a woman.
    Perpoint T, Argaud L, Blanc Q, Robert D.
    Intensive Care Med; 2001 Dec 01; 27(12):1962. PubMed ID: 11797036
    [No Abstract] [Full Text] [Related]

  • 14. [Hyperammonaemic coma after valproate therapy as adult onset of ornithine transcarbamylase deficiency].
    Padilla Mde L, Miguélez M, Riverola A, Bueno J.
    Med Clin (Barc); 2002 Feb 16; 118(5):199. PubMed ID: 11852003
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  • 16. Hyperammonemia-induced encephalopathy due to ornithine transcarbamylase deficiency in an adult woman: identification of novel missense mutations.
    Tanaka A, Wada T, Maruyama M, Tanaka A, Takikawa H, Komatsu Y.
    J Gastroenterol; 2005 Jan 16; 40(1):106-7. PubMed ID: 15692798
    [No Abstract] [Full Text] [Related]

  • 17. 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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  • 18. The phenotype of ostensibly healthy women who are carriers for ornithine transcarbamylase deficiency.
    Maestri NE, Lord C, Glynn M, Bale A, Brusilow SW.
    Medicine (Baltimore); 1998 Nov 30; 77(6):389-97. PubMed ID: 9854602
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  • 19. Hyperammonemia in women with a mutation at the ornithine carbamoyltransferase locus. A cause of postpartum coma.
    Arn PH, Hauser ER, Thomas GH, Herman G, Hess D, Brusilow SW.
    N Engl J Med; 1990 Jun 07; 322(23):1652-5. PubMed ID: 2342525
    [No Abstract] [Full Text] [Related]

  • 20. Hyperammonemia in ornithine transcarbamylase-deficient recipients following living donor liver transplantation from heterozygous carrier donors.
    Rahayatri TH, Uchida H, Sasaki K, Shigeta T, Hirata Y, Kanazawa H, Mali V, Fukuda A, Sakamoto S, Kasahara M.
    Pediatr Transplant; 2017 Feb 07; 21(1):. PubMed ID: 27891735
    [Abstract] [Full Text] [Related]


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