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Journal Abstract Search

259 related items for PubMed ID: 19640662

  • 1. 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]

  • 2. Ornithine transcarbamylase deficiency presenting with acute reversible cortical blindness.
    Prasun P, Altinok D, Misra VK.
    J Child Neurol; 2015 May; 30(6):782-5. PubMed ID: 24850570
    [Abstract] [Full Text] [Related]

  • 3. [Acute hyperammonemic encephalopathy in ornithine transcarbamylase deficiency].
    Sánchez Sánchez V, Palomino García A, Pereira Cunill JL, Rodríguez Uranga JJ.
    Neurologia; 2009 Jun; 24(5):345-6. PubMed ID: 20050118
    [No Abstract] [Full Text] [Related]

  • 4. 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]

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

  • 6. 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]

  • 7. 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]

  • 8. 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]

  • 9. Osmotic demyelination syndrome as a consequence of treating hyperammonemia in a patient with ornithine transcarbamylase deficiency.
    Cardenas JF, Bodensteiner JB.
    J Child Neurol; 2009 Jul; 24(7):884-6. PubMed ID: 19225137
    [Abstract] [Full Text] [Related]

  • 10. Late-onset ornithine transcarbamylase deficiency: treatment and outcome of hyperammonemic crisis.
    Bergmann KR, McCabe J, Smith TR, Guillaume DJ, Sarafoglou K, Gupta S.
    Pediatrics; 2014 Apr; 133(4):e1072-6. PubMed ID: 24616362
    [Abstract] [Full Text] [Related]

  • 11. 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; 40(1):106-7. PubMed ID: 15692798
    [No Abstract] [Full Text] [Related]

  • 12. Ornithine transcarbamylase deficiency presenting as hepatitis.
    Aronson PL, Mistry RD.
    Pediatr Emerg Care; 2011 Jun; 27(6):527-9. PubMed ID: 21642786
    [Abstract] [Full Text] [Related]

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

  • 14. [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; 192(3):281-5. PubMed ID: 7191930
    [Abstract] [Full Text] [Related]

  • 15. 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; 33(3):474.e1-3. PubMed ID: 25227973
    [Abstract] [Full Text] [Related]

  • 16. Late-onset ornithine transcarbamylase deficiency associated with hyperammonemia.
    Daijo K, Kawaoka T, Nakahara T, Nagaoki Y, Tsuge M, Hiramatsu A, Imamura M, Kawakami Y, Aikata H, Hara K, Tajima G, Kobayashi M, Chayama K.
    Clin J Gastroenterol; 2017 Aug; 10(4):383-387. PubMed ID: 28597413
    [Abstract] [Full Text] [Related]

  • 17. Successful early management of a female patient with a metabolic stroke due to ornithine transcarbamylase deficiency.
    Tummolo A, Favia V, Bellantuono R, Bellino V, Ranieri A, Morrone A, De Palo T, Papadia F.
    Pediatr Emerg Care; 2013 May; 29(5):656-8. PubMed ID: 23640148
    [Abstract] [Full Text] [Related]

  • 18. 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]

  • 19. Adult-onset ornithine transcarbamylase deficiency as a rare cause of fatal hyperammonaemia.
    Durer S, Durer C, Hoilat GJ.
    Lancet; 2021 Aug 28; 398(10302):e11. PubMed ID: 34454677
    [No Abstract] [Full Text] [Related]

  • 20. 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 28; 96(11):1512-7. PubMed ID: 24428103
    [Abstract] [Full Text] [Related]

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