Calcitonin receptor gene polymorphism: A possible genetic marker for patients with calcium oxalate stones

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题名:	Calcitonin receptor gene polymorphism: A possible genetic marker for patients with calcium oxalate stones
作者:	Chen, WC;Wu, HC;Lu, HF;Chen, HY;Tsai, FJ
贡献者:	附設醫院;China Med Coll Hosp, Coll Med, Dept Urol, Taichung, Taiwan;China Med Coll Hosp, Coll Med, Dept Obstet & Gynecol, Taichung, Taiwan;China Med Coll Hosp, Coll Med, Dept Med Genet, Taichung, Taiwan;Natl Tsing Hua Univ, Inst Life Sci, Hsinchu, Taiwan
日期:	2001
上传时间:	2010-09-24 14:17:00 (UTC+8)
出版者:	KARGER
摘要:	Objective. To test the hypothesis that syndrome X is a systemic vascular disorder, the authors studied 40 patients with this diagnosis using technetium-99m hexamethylpropylene amine oxime and single photon emission computed tomography (SPECT) brain images. Twenty-three of 25 cases with definite myocardial perfusion defects diagnosed by thallium-201 myocardial perfusion SPECT also had multiple hypoperfusion areas in the brain versus 2 of 15 patients without thallium myocardial defects. The parietal lobes were the most common hypoperfusion areas, and cerebellum was the least common. Syndrome X is a systemic vascular disorder with a high incidence of hypoperfusion lesions of the brain and is usually coincident with myocardial defects.
關聯:	EUROPEAN UROLOGY 39(6):716-719
显示于类别:	[台中附設醫院] 期刊論文

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