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浏览/检索结果: 共15条，第1-10条 帮助 限定条件 发表日期：2015    专题：中国医学科学院 北京协和医学院    第一署名单位    第一作者单位    通讯作者单位     已选(0)清除 条数/页：5101520253035404550556065707580859095100   排序方式：请选择作者升序作者降序题名升序题名降序发表日期升序发表日期降序提交时间升序提交时间降序 A Novel Missense Mutation In The NBCe1 Gene (SLC4A4) And A Novel Mode Of Inheritance For Proximal Renal Tubular Acidosis (pRTA) 期刊论文 2015, 卷号: 29 作者:  Myers, Evan;  Yuan, Lu;  Felmlee, Melanie;  Lin, Yuan-Yuan;  Jiang, Yan 收藏  |  浏览/下载：3/0  |  提交时间：2020/01/04 Physical performance and life quality in postmenopausal women supplemented with vitamin D: a two-year prospective study 期刊论文 2015, 卷号: 36, 期号: 9, 页码: 1065-1073 作者:  Gao, Li-hong;  Zhu, Wen-jun;  Liu, Yu-juan;  Gu, Jie-mei;  Zhang, Zhen-lin 收藏  |  浏览/下载：7/0  |  提交时间：2020/01/04 postmenopausal women  cholecalciferol  calcitriol  25-hydroxyvitamin D  parathyroid hormone  beta-CTX  P1NP  bone turnover  muscle strength  quality of life   A Mutation in CTSK Gene in an Autosomal Recessive Pycnodysostosis Family of Chinese Origin 期刊论文 2015, 卷号: 96, 期号: 5, 页码: 373-378 作者:  Huang, Xianglan;  Qi, Xuan;  Li, Mei;  Wang, Ou;  Jiang, Yan 收藏  |  浏览/下载：2/0  |  提交时间：2020/01/13 Pycnodysostosis  CTSK  Cathepsin K deficiency  Acro-osteolysis  Osteoclast   SOST polymorphisms and response to alendronate treatment in postmenopausal Chinese women with osteoporosis 期刊论文 2015, 卷号: 16, 期号: 10, 页码: 1077-1087 作者:  Zhou, Pei-ran;  Xu, Xiao-jie;  Zhang, Zhen-lin;  Liao, Er-yuan;  Chen, De-cai 收藏  |  浏览/下载：2/0  |  提交时间：2020/01/13 osteoporosis  polymorphisms  response to alendronate  SOST gene   Low-dose adefovir dipivoxil may induce Fanconi syndrome: clinical characteristics and long-term follow-up for Chinese patients 期刊论文 2015, 卷号: 20, 期号: 6, 页码: 603-611 作者:  Xu, Li-Jun;  Jiang, Yan;  Liao, Ruo-Xi;  Zhang, Hua-Bing;  Mao, Jiang-Feng 收藏  |  浏览/下载：2/0  |  提交时间：2020/01/13 First Report of a Novel Missense CLDN19 Mutations Causing Familial Hypomagnesemia with Hypercalciuria and Nephrocalcinosis in a Chinese Family 期刊论文 2015, 卷号: 96, 期号: 4, 页码: 265-273 作者:  Yuan, Tao;  Pang, Qianqian;  Xing, Xiaoping;  Wang, Xi;  Li, Yuhui 收藏  |  浏览/下载：2/0  |  提交时间：2020/01/13 Hypomagnesemia  Hypercalciuria  CLDN19 gene  Mutation   A Novel Missense Mutation In The NBCe1 Gene (SLC4A4) And A Novel Mode Of Inheritance For Proximal Renal Tubular Acidosis (pRTA) 会议论文 FASEB JOURNAL, 2015-04-01 作者:  Myers, Evan;  Yuan, Lu;  Felmlee, Melanie;  Lin, Yuan-Yuan;  Jiang, Yan 收藏  |  浏览/下载：2/0  |  提交时间：2020/01/13 MEN1 c.825-1G>A mutation in a family with multiple endocrine neoplasia type 1: A case report 期刊论文 2015, 卷号: 12, 期号: 4, 页码: 6152-6156 作者:  Ning, Zhiwei;  Wang, Ou;  Meng, Xunwu;  Xing, Xiaoping;  Xia, Weibo 收藏  |  浏览/下载：3/0  |  提交时间：2020/01/13 multiple endocrine neoplasia type 1  MEN1  mutation  treatment  follow up   Genomic Analyses Reveal Mutational Signatures and Frequently Altered Genes in Esophageal Squamous Cell Carcinoma 期刊论文 2015, 卷号: 96, 期号: 4, 页码: 597-611 作者:  Zhang, Ling;  Zhou, Yong;  Cheng, Caixia;  Cui, Heyang;  Cheng, Le 收藏  |  浏览/下载：31/0  |  提交时间：2020/01/13 Aromatase deficiency in a Chinese adult man caused by novel compound heterozygous CYP19A1 mutations: Effects of estrogen replacement therapy on the bone, lipid, liver and glucose metabolism 期刊论文 2015, 卷号: 399, 期号: C, 页码: 32-42 作者:  Chen, Zhike;  Wang, Ou;  Nie, Min;  Elison, Kathleen 收藏  |  浏览/下载：10/0  |  提交时间：2020/01/13 Aromatase  CYP19A1  Aromatase deficiency  Metabolic syndrome  Insulin resistance  Estrogen replacement