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Primary hyperparathyroidism in Chinese children and adolescents: A single-centre experience at Peking Union Medical College Hospital 期刊论文
2017, 卷号: 87, 期号: 6, 页码: 865-873
作者:  Wang, Wenbo;  Kong, Jing;  Nie, Min;  Jiang, Yan;  Li, Mei
收藏  |  浏览/下载:4/0  |  提交时间:2020/01/03
Atypical skeletal manifestations of rickets in a familial hypocalciuric hypercalcemia patient 期刊论文
2017, 卷号: 5, 期号: 3, 页码: 17001
作者:  Wu, Bo;  Wang, Ou;  Jiang, Yan;  Li, Mei;  Xing, Xiaoping
收藏  |  浏览/下载:3/0  |  提交时间:2020/01/04
Associations between FGF21, osteonectin and bone turnover markers in type 2 diabetic patients with albuminuria 期刊论文
2017, 卷号: 31, 期号: 3, 页码: 583-588
作者:  Xu Lingling;  Niu Meng;  Yu Weihong;  Xia Weibo;  Gong Fengying
收藏  |  浏览/下载:3/0  |  提交时间:2020/01/04
Familial Early-Onset Paget's Disease of Bone Associated with a Novel hnRNPA2B1 Mutation 期刊论文
2017, 卷号: 101, 期号: 2, 页码: 159-169
作者:  Qi Xuan;  Pang Qianqian;  Wang Jiawei;  Zhao Zhen;  Wang Ou
收藏  |  浏览/下载:3/0  |  提交时间:2020/01/04
Pharmacological Treatment of Bone Loss 期刊论文
2017, 卷号: 23, 期号: 41, 页码: 6298-6301
作者:  Pang, Rui;  Xia, Weibo
收藏  |  浏览/下载:2/0  |  提交时间:2020/01/04
The Asian Federation of Osteoporosis Societies' call to action to improve the undertreatment of osteoporosis in Asia 期刊论文
2017, 卷号: 3, 期号: 4, 页码: 161-163
作者:  Yeap Swan Sim;  Jaisamrarn Unnop;  Park Ye-Soo;  Takeuchi Yasuhiro;  Xia Weibo
收藏  |  浏览/下载:2/0  |  提交时间:2020/01/04
Earlier onset age of p.R179 than p.R176 mutation of FGF23 gene in autosomal dominant hypophosphatemic rickets: Analysis of 6 Chinese pedigrees and review of the literature. 会议论文
JOURNAL OF BONE AND MINERAL RESEARCH, 2017-12-01
作者:  Zhao, Zhen;  Liu, Chang;  Wang, Ou;  Li, Mei;  Xing, Xiaoping
收藏  |  浏览/下载:2/0  |  提交时间:2020/01/04
Etiology Identification and Serum FGF-23 Measurement in Ten Patients with Fanconi Syndrome. 会议论文
JOURNAL OF BONE AND MINERAL RESEARCH, 2017-12-01
作者:  Du, Juan;  Zhang, Cong;  Pang, Qian-qian;  Jiang, Yan;  Wang, Ou
收藏  |  浏览/下载:10/0  |  提交时间:2020/01/04
Earlier onset age of p.R179 than p.R176 mutation of FGF23 gene in autosomal dominant hypophosphatemic rickets: Analysis of 6 Chinese pedigrees and review of the literature. 期刊论文
2017, 卷号: 32, 页码: S390-S391
作者:  Zhao, Zhen;  Liu, Chang;  Wang, Ou;  Li, Mei;  Xing, Xiaoping
收藏  |  浏览/下载:6/0  |  提交时间:2020/01/04
Etiology Identification and Serum FGF-23 Measurement in Ten Patients with Fanconi Syndrome. 期刊论文
2017, 卷号: 32, 页码: S125-S125
作者:  Du, Juan;  Zhang, Cong;  Pang, Qian-qian;  Jiang, Yan;  Wang, Ou
收藏  |  浏览/下载:2/0  |  提交时间:2020/01/04


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