These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

370 related items for PubMed ID: 17763159

  • 1. 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; 29(6):661-5. PubMed ID: 17763159
    [Abstract] [Full Text] [Related]

  • 2. Continuous arteriovenous hemodiafiltration in the acute treatment of hyperammonaemia due to ornithine transcarbamylase deficiency.
    Chen CY, Chen YC, Fang JT, Huang CC.
    Ren Fail; 2000 Nov; 22(6):823-36. PubMed ID: 11104170
    [Abstract] [Full Text] [Related]

  • 3. 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]

  • 4. [Hyperammonemia type II as an example of urea cycle disorder].
    Hawrot-Kawecka AM, Kawecki GP, Duława J.
    Wiad Lek; 2006 Jan; 59(7-8):512-5. PubMed ID: 17209350
    [Abstract] [Full Text] [Related]

  • 5.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 6. Fatal cerebral edema from late-onset ornithine transcarbamylase deficiency in a juvenile male patient receiving valproic acid.
    Thakur V, Rupar CA, Ramsay DA, Singh R, Fraser DD.
    Pediatr Crit Care Med; 2006 May; 7(3):273-6. PubMed ID: 16575347
    [Abstract] [Full Text] [Related]

  • 7. Successful continuous venovenous hemofiltration in a neonate with hyperammonemia from ornithine transcabamylase deficiency.
    Pirojsakul K, Tangnararatchakit K, Vaewpanich J, Niyomvit K, Chanhom D, Udomchaisakul R, Tapaneya-Olarn W, Wattanasirichaigoon D.
    J Med Assoc Thai; 2013 Nov; 96(11):1512-7. PubMed ID: 24428103
    [Abstract] [Full Text] [Related]

  • 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
    [Abstract] [Full Text] [Related]

  • 9. High-volume continuous venovenous hemofiltration as an effective therapy for acute management of inborn errors of metabolism in young children.
    Lai YC, Huang HP, Tsai IJ, Tsau YK.
    Blood Purif; 2007 Apr 01; 25(4):303-8. PubMed ID: 17643056
    [Abstract] [Full Text] [Related]

  • 10.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 11.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 12. [Hyperammonemia in the newborn through ornithine transcarbamylase deficiency (author's transl)].
    Plöchl E, Hilbe W, Bachmann C.
    Padiatr Padol; 1981 Apr 01; 16(2):179-88. PubMed ID: 7243329
    [Abstract] [Full Text] [Related]

  • 13. The therapy of hyperammonemia due to ornithine transcarbamylase defiency in a male neonate.
    Snyderman SE, Sansaricq C, Phansalkar SV, Schacht RC, Norton PM.
    Pediatrics; 1975 Jul 01; 56(1):65-73. PubMed ID: 1153252
    [Abstract] [Full Text] [Related]

  • 14.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 15.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 16. Acrodermatitis enteropathica-like dermatosis associated with ornithine transcarbamylase deficiency.
    Pascual JC, Matarredona J, Mut J.
    Pediatr Dermatol; 2007 Jul 01; 24(4):394-6. PubMed ID: 17845164
    [Abstract] [Full Text] [Related]

  • 17. [Hyperammonemia due to ornithine transcarbamylase deficiency--a cause of lethal metabolic crisis during the newborn period and infancy (author's transl)].
    Schuchmann L, Colombo JP, Fischer H.
    Klin Padiatr; 1980 May 01; 192(3):281-5. PubMed ID: 7191930
    [Abstract] [Full Text] [Related]

  • 18. Amino acid and DNA analyses in a family with ornithine transcarbamylase deficiency.
    Hou JW, Wang TR.
    J Formos Med Assoc; 1996 Feb 01; 95(2):144-7. PubMed ID: 9064003
    [Abstract] [Full Text] [Related]

  • 19. [Neonatal hyperammonemia due to ornithine transcarbamylase deficiency (author's transl)].
    del Valle JA, Urbón A, García MJ, Cuadrado P, Ugarte M.
    An Esp Pediatr; 1982 May 01; 16(5):416-20. PubMed ID: 7114619
    [Abstract] [Full Text] [Related]

  • 20. 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 01; 47(Pt 3):279-81. PubMed ID: 20406775
    [Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 19.