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120 related items for PubMed ID: 24428103

  • 1. 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]

  • 2. 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 Nov; 25(4):303-8. PubMed ID: 17643056
    [Abstract] [Full Text] [Related]

  • 3. 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]

  • 4. 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]

  • 5. 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]

  • 6. [Hemofiltration in acute neonatal metabolic crisis].
    Ring E, Zobel G.
    Wien Klin Wochenschr; 1992 Nov; 104(21):674-7. PubMed ID: 1475972
    [Abstract] [Full Text] [Related]

  • 7. Hyperammonemia in a patient with late-onset ornithine carbamoyltransferase deficiency.
    Choi DE, Lee KW, Shin YT, Na KR.
    J Korean Med Sci; 2012 May; 27(5):556-9. PubMed ID: 22563224
    [Abstract] [Full Text] [Related]

  • 8. 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]

  • 9. 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]

  • 10. 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]

  • 11. 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]

  • 12. Acute onset of ornithine transcarbamylase deficiency after total anomalous pulmonary venous connection repair to a 2-day-old neonate.
    Yoshida H, Iwata Y, Fuchigami T, Katagiri J.
    Cardiol Young; 2023 Sep; 33(9):1775-1776. PubMed ID: 37042609
    [Abstract] [Full Text] [Related]

  • 13. 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
    [Abstract] [Full Text] [Related]

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

  • 15. 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]

  • 16. Intermittent hyperammonemic encephalopathy in a child with ornithine transcarbamylase deficiency.
    Gulati S, Menon S, Kabra M, Kalra V.
    Indian J Pediatr; 2004 Jul; 71(7):645-7. PubMed ID: 15280615
    [Abstract] [Full Text] [Related]

  • 17. Ammonia detoxification by continuous venovenous haemofiltration in an infant with urea cycle defect.
    Chan WK, But WM, Law CW.
    Hong Kong Med J; 2002 Jun; 8(3):207-10. PubMed ID: 12055368
    [Abstract] [Full Text] [Related]

  • 18. Hyperammonemic Encephalopathy Mimicking Ornithine Transcarbamylase Deficiency in Fibrolamellar Hepatocellular Carcinoma: Successful Treatment with Continuous Venovenous Hemofiltration and Ammonia Scavengers.
    Lee JS, Jin HY, Ko JM, Kim SH, Han N, Park BK, Park M, Park HJ, Lee JA.
    Cancer Res Treat; 2021 Jan; 53(1):283-288. PubMed ID: 32898940
    [Abstract] [Full Text] [Related]

  • 19. 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; 56(1):65-73. PubMed ID: 1153252
    [Abstract] [Full Text] [Related]

  • 20. [Neonate-onset ornithine transcarbamylase deficiency].
    Gao RW, Ba Y, Zhang R, Cao Y, Yang L, Wu BB, Zhou WH, Zhou JG.
    Zhongguo Dang Dai Er Ke Za Zhi; 2023 Apr 15; 25(4):431-435. PubMed ID: 37073851
    [Abstract] [Full Text] [Related]

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