Polymorphism of transmembrane region of MICA gene and Kawasaki disease

中國醫藥大學機構典藏 China Medical University Repository, Taiwan > 台中附設醫院 > 期刊論文 > Item 310903500/30415

jsp.display-item.identifier=請使用永久網址來引用或連結此文件: http://ir.cmu.edu.tw/ir/handle/310903500/30415

题名:	Polymorphism of transmembrane region of MICA gene and Kawasaki disease
作者:	Huang, FY;Lee, YJ;Chen, MR;Hsu, CH;Lin, SP;Sung, TC;Chang, SC;Chang, JG
贡献者:	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
日期:	2000
上传时间:	2010-09-24 14:54:58 (UTC+8)
出版者:	KARGER
摘要:	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.
關聯:	EXPERIMENTAL AND CLINICAL IMMUNOGENETICS 17(3):130-137
显示于类别:	[台中附設醫院] 期刊論文

文件中的档案:

没有与此文件相关的档案.

在CMUR中所有的数据项都受到原著作权保护.

TAIR相关文章