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[会议论文] 作者:Guiyan Han,Xiaoping Xing,Fengying Gong,Huijuan Zhu, 来源:第六届华夏内分泌大会 年份:2010
[期刊论文] 作者:Bo Wu,Ou Wang,Yan Jiang,Mei Li,Xiaoping Xing,Weibo Xia,, 来源:Bone Research 年份:2017
Familial hypocalciuric hypercalcemia(FHH) is caused by inactivating mutations in the calcium-sensing receptor(Ca SR) gene. The loss of function of Ca SR present...
[会议论文] 作者:Jianping Xu,Fan Ping,Mei Li,Wei Yu,Weibo Xia,Xiaoping Xing, 来源:第六届华夏内分泌大会 年份:2010
[会议论文] 作者:Chunyan Wang,Ou Wang,Nie Min,Quancai Cui,Xunwu Meng,Xiaoping Xing,Heng Guan, 来源:第六届华夏内分泌大会 年份:2010
[会议论文] 作者:Mei Li,Xiaoping Xing,Xunwu Meng,Weibo Xia,Zhenlin Zhang,Zhonglan Zhang,Jianli Liu, 来源:第三届国际骨质疏松及骨矿盐疾病学术会议 年份:2007
[会议论文] 作者:Mei Li,Xiaoping Xing,Zhenlin Zhang,Zhonglan Zhang,Xunwu Meng,Jianli Liu,Weibo Xia, 来源:第三届国际骨质疏松及骨矿盐疾病学术会议 年份:2007
[会议论文] 作者:Chunyan Wang,Ou Wang,Nie Min,Heng Guan,Quancai Cui,Xunwu Meng,Xiaoping Xing, 来源:第六届华夏内分泌大会 年份:2010
[期刊论文] 作者:Qianqian Pang,Xuan Qi,Yan Jiang,Ou Wang,Mei Li,Xiaoping Xing,Jin Dong,Weibo Xia,, 来源:Bone Research 年份:2016
Hereditary vitamin D-resistant rickets(HVDRR) is a rare autosomal recessive disorder characterized by severe rickets,hypocalcemia,hypophosphatemia,secondary hyp...
[会议论文] 作者:Nan Li,Jing Sun,Zhen Zhao,Mei Li,Ou Wang,Yan Jiang,Xiaoping Xing,Weibo Xia, 来源:第六届国际骨质疏松及骨矿盐疾病学术会议 年份:2012
[会议论文] 作者:Wen Xu,Weibo Xia,Jing Sun,Mei Li,Yan Jiang,Ou Wang,Xiaoping Xing,Xueying Zhou, 来源:第六届国际骨质疏松及骨矿盐疾病学术会议 年份:2012
[会议论文] 作者:Guiyan Han,Ou Wang,Min Nie,Yah Zhu,Xunwu Meng,Yingying Hu,Huaicheng Liu,Xiaoping Xing, 来源:中华医学会第七次全国骨质疏松和骨矿盐疾病学术会议 年份:2013
[会议论文] 作者:Yue Sun,Weibo Xia,Mei Li,Yan Jiang,Ou Wang,Xiaoping Xing,Xunwu Meng,Zhenlin Zhang, 来源:International Conference on Osteoporosis and Bone Research 2 年份:2008
[会议论文] 作者:Ou WANG,Xiaoping XING,Xunwu MENG,Weibo XIA,Mei LI,Yan JIANG,Yingying HU,Huaicheng LIU, 来源:第三届国际骨质疏松及骨矿盐疾病学术会议 年份:2007
[会议论文] 作者:Yue Sun,Weibo Xia,Mei Li,Yan Jiang,Ou Wang,Xiaoping Xing,Zhenlin Zhang,Xunwu Meng, 来源:International Conference on Osteoporosis and Bone Research 2 年份:2008
[会议论文] 作者:Guiyan Han,Ou Wang,Min Nie,Yah Zhu,Xunwu Meng,Yingying Hu,Huaicheng Liu,Xiaoping Xing, 来源:中华医学会第七次全国骨质疏松和骨矿盐疾病学术会议 年份:2013
Objective To investigate the distribution of A986S and R990Gpolymorphisms of CASR gene in Chinese population, and their relationship with the risk and clinical phenotypes of primary hyperparathyroidis...
[会议论文] 作者:Nan Li,Min Nie,Mei Li,Yan Jiang,Xiaoping Xing,Ou Wang,Chunlin Li,Weibo Xia, 来源:中华医学会第七次全国骨质疏松和骨矿盐疾病学术会议 年份:2013
Objective Acrodysostosis (ACRDYS) is a rare skeletal dysplasia, some of which have multiple hormone resistance.PRKAR1A gene, which encodes the type I-alpha regulatory subunits of cAMPdependent protein...
[会议论文] 作者:Wen Xu,Weibo Xia,Jing Sun,Mei Li,Yan Jiang,Ou Wang,Xiaoping Xing,Xueying Zhou, 来源:第六届国际骨质疏松及骨矿盐疾病学术会议 年份:2012
[会议论文] 作者:Yi Liu,Mei Li,Peiran Zhou,Fang Lv,Weibo Xia,Yan Jiang,Oui Wang,Xiaoping Xing,WeiYU, 来源:第七届国际骨质疏松及骨矿盐疾病学术会议 年份:2014
[会议论文] 作者:Yi Liu,Mei Li,Peiran Zhou,Fang Lv,Weibo Xia,WeiYU,Yan Jiang,Oui Wang,Xiaoping Xing, 来源:第七届国际骨质疏松及骨矿盐疾病学术会议 年份:2014
Background: Osteogenesis imperfecta (OI) type Ⅴ is rare,autosomal dominant inherited disease characterized by multiple fractures, radial head dislocation, intraosseous membrane calcification of the fo...
[会议论文] 作者:Lanwen Han,Yingying Hu,Min Nie,Weibo Xia,Xiaoping Xing,Yan Jiang,Ou Wang,Mei Li,Ling Xu, 来源:中华医学会第四届骨质疏松和骨矿盐疾病中青年学术会议 年份:2012
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