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ZOLEDRONIC ACID VERSUS ALENDRONATE IN THE TREATMENT OF CHILDREN WITH OSTEOGENESIS IMPERFECTA: A 2-YEAR CLINICAL STUDY 期刊论文
2018, 卷号: 24, 期号: 2, 页码: 179-188
作者:  Lv, Fang;  Liu, Yi;  Xu, Xiaojie;  Song, Yuwen;  Li, Lujiao
收藏  |  浏览/下载:2/0  |  提交时间:2020/01/03
Osteogenesis imperfecta type V: Genetic and clinical findings in eleven Chinese patients 期刊论文
2016, 卷号: 462, 页码: 201-209
作者:  Liu, Yi;  Wang, Jiawei;  Ma, Doudou;  Lv, Fang;  Xu, Xiaojie
收藏  |  浏览/下载:8/0  |  提交时间:2020/01/04
Genotype-phenotype analysis of a rare type of osteogenesis imperfecta in four Chinese families with WNT1 mutations 期刊论文
2016, 卷号: 461, 页码: 172-180
作者:  Liu, Yi;  Song, Lijie;  Ma, Doudou;  Lv, Fang;  Xu, Xiaojie
收藏  |  浏览/下载:2/0  |  提交时间:2020/01/04
EFFECTS OF LONG-TERM ALENDRONATE TREATMENT ON A LARGE SAMPLE OF PEDIATRIC PATIENTS WITH OSTEOGENESIS IMPERFECTA 期刊论文
2016, 卷号: 22, 期号: 12, 页码: 1369-1376
作者:  Lv, Fang;  Liu, Yi;  Xu, Xiaojie;  Wang, Jianyi;  Ma, Doudou
收藏  |  浏览/下载:2/0  |  提交时间:2020/01/04
Association of farnesyl diphosphate synthase polymorphisms and response to alendronate treatment in Chinese postmenopausal women with osteoporosis 期刊论文
2014, 卷号: 127, 期号: 4, 页码: 662-668
作者:  Liu Yi;  Liu Haijuan;  Li Mei;  Zhou Peiran;  Xing Xiaoping
收藏  |  浏览/下载:4/0  |  提交时间:2020/01/13
Novel Mutations in FKBP10 and PLOD2 Cause Rare Bruck Syndrome in Chinese Patients 期刊论文
2014, 卷号: 9, 期号: 9, 页码: e107594
作者:  Zhou, Peiran;  Liu, Yi;  Lv, Fang;  Nie, Min;  Jiang, Yan
收藏  |  浏览/下载:13/0  |  提交时间:2020/01/13


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