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Journal Abstract Search

304 related items for PubMed ID: 17845164

  • 1. Acrodermatitis enteropathica-like dermatosis associated with ornithine transcarbamylase deficiency.
    Pascual JC, Matarredona J, Mut J.
    Pediatr Dermatol; 2007; 24(4):394-6. PubMed ID: 17845164
    [Abstract] [Full Text] [Related]

  • 2. A case of acrodermatitis enteropathica-like dermatosis caused by ornithine transcarbamylase deficiency.
    Lee JY, Chang SE, Suh CW, Choi JH, Sung KJ, Moon KC, Koh JK.
    J Am Acad Dermatol; 2002 Jun; 46(6):965-7. PubMed ID: 12063505
    [No Abstract] [Full Text] [Related]

  • 3. Urea cycle disorders in Thai infants: a report of 5 cases.
    Wasant P, Srisomsap C, Liammongkolkul S, Svasti J.
    J Med Assoc Thai; 2002 Aug; 85 Suppl 2():S720-31. PubMed ID: 12403252
    [Abstract] [Full Text] [Related]

  • 4. Fatal ammonia toxicity in an adult due to an undiagnosed urea cycle defect: under-recognition of ornithine transcarbamylase deficiency.
    Thurlow VR, Asafu-Adjaye M, Agalou S, Rahman Y.
    Ann Clin Biochem; 2010 May; 47(Pt 3):279-81. PubMed ID: 20406775
    [Abstract] [Full Text] [Related]

  • 5. Aminograms during continuous hemodiafiltration in the treatment of hyperammonemia due to ornithine transcarbamylase deficiency.
    Chen CY, Tsai TC, Lee WJ, Chen HC.
    Ren Fail; 2007 May; 29(6):661-5. PubMed ID: 17763159
    [Abstract] [Full Text] [Related]

  • 6. Acrodermatitis enteropathica-like eruption in metabolic disorders: acrodermatitis dysmetabolica is proposed as a better term.
    Tabanlioğlu D, Ersoy-Evans S, Karaduman A.
    Pediatr Dermatol; 2009 May; 26(2):150-4. PubMed ID: 19419460
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  • 8. Vomiting, ataxia, and altered mental status in an adolescent: late-onset ornithine transcarbamylase deficiency.
    Myers JH, Shook JE.
    Am J Emerg Med; 1996 Oct; 14(6):553-7. PubMed ID: 8857803
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  • 10. Ammonia toxicity and its prevention in inherited defects of the urea cycle.
    Walker V.
    Diabetes Obes Metab; 2009 Sep; 11(9):823-35. PubMed ID: 19531057
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  • 12. Studies of the cause and treatment of hyperammonemia in females with ornithine transcarbamylase deficiency.
    Glasgow AM, Kraegel JH, Schulman JD.
    Pediatrics; 1978 Jul; 62(1):30-7. PubMed ID: 683780
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  • 13. Parieto-occipital encephalomalacia in neonatal hyperammonemia with ornithine transcarbamylase deficiency: A case report.
    Okanishi T, Ito T, Nakajima Y, Ito K, Kakita H, Yamada Y, Kobayashi S, Ando N, Togari H.
    Brain Dev; 2010 Aug; 32(7):567-70. PubMed ID: 19640662
    [Abstract] [Full Text] [Related]

  • 14. Acrodermatitis enteropathica-like eruptions in a child with Hartnup disease.
    Seyhan ME, Selimoğlu MA, Ertekin V, Fidanoğlu O, Altinkaynak S.
    Pediatr Dermatol; 2006 Aug; 23(3):262-5. PubMed ID: 16780476
    [Abstract] [Full Text] [Related]

  • 15. Blood levels of ammonia and nitrogen scavenging amino acids in patients with inherited hyperammonemia.
    Tuchman M, Yudkoff M.
    Mol Genet Metab; 1999 Jan; 66(1):10-5. PubMed ID: 9973542
    [Abstract] [Full Text] [Related]

  • 16. [An anesthetic experience with a patient with ornithine transcarbamylase deficiency].
    Hirota K, Shiga T, Kimura K, Matsuki A, Oyama T.
    Masui; 1989 Jan; 38(1):98-101. PubMed ID: 2709615
    [Abstract] [Full Text] [Related]

  • 17. Ornithine transcarbamylase deficiency diagnosed in pregnancy.
    Celik O, Buyuktas D, Aydin A, Acbay O.
    Gynecol Endocrinol; 2011 Dec; 27(12):1052-4. PubMed ID: 21736537
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  • 19. 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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