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    CMUR > China Medical University Hospital > Jurnal articles >  Item 310903500/30415
    Please use this identifier to cite or link to this item: http://ir.cmu.edu.tw/ir/handle/310903500/30415


    Title: Polymorphism of transmembrane region of MICA gene and Kawasaki disease
    Authors: Huang, FY;Lee, YJ;Chen, MR;Hsu, CH;Lin, SP;Sung, TC;Chang, SC;Chang, JG
    Contributors: 附設醫院醫研部;China Med Coll Hosp, Dept Med Res, Div Mol Med, Taichung, Taiwan;Mackay Mem Hosp, Dept Pediat, Taipei, Taiwan;Mackay Mem Hosp, Dept Med Res, Taipei, Taiwan;Taipei Med Coll, Dept Pediat, Taipei, Taiwan;Shin Kong Wu Ho Su Mem Hosp, Dept Pediat, Taipei, Taiwan
    Date: 2000
    Issue Date: 2010-09-24 14:54:58 (UTC+8)
    Publisher: KARGER
    Abstract: In 30 patients with syndrome X, esophageal motility was evaluated by radionuclide esophageal transit test (RETT). Esophageal motility measurements included esophageal mean transit time (MTT), residual fraction (RF), and retrograde index (RI). In comparison with 25 age- and sex-matched healthy volunteers, 66% of the patients with syndrome X had abnormal RETT findings including 50% of cases with longer MTT, 50% of cases with higher RF, and 33% of cases with higher RI. In addition, the mean values of MTT, RF, and RI in patients with syndrome X were significantly higher than those of healthy volunteers. We conclude that abnormal esophageal motility occurred in a large portion of syndrome X patients based on an simple and noninvasive RETT. Copyright (C) 2000 S. Karger AG, Basel.
    Relation: EXPERIMENTAL AND CLINICAL IMMUNOGENETICS 17(3):130-137
    Appears in Collections:[China Medical University Hospital] Jurnal articles

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