CORC

在结果中检索

CORC

浏览/检索结果: 共7条，第1-7条 帮助

限定条件                
已选(0)清除 条数/页：   排序方式：
Up-regulation of FOXD1 by YAP alleviates senescence and osteoarthritis 期刊论文
PLOS BIOLOGY, 2019, 卷号: 17, 期号: 4
作者:  Fu, Lina;  Hu, Yuqiong;  Song, Moshi;  Liu, Zunpeng;  Zhang, Weiqi
收藏  |  浏览/下载：43/0  |  提交时间：2019/12/05
Combined measurement of plasma cystatin C and low-density lipoprotein cholesterol: A valuable tool for evaluating progressive supranuclear palsy 期刊论文
PARKINSONISM & RELATED DISORDERS, 2018, 卷号: 52
作者:  Weng, Ruihui;  Wei, Xiaobo;  Yu, Bin;  Zhu, Shuzhen;  Yang, Xiaohua
收藏  |  浏览/下载：10/0  |  提交时间：2019/12/05
Management Recommendations on Sleep Disturbance of Patients with Parkinson's Disease 期刊论文
CHINESE MEDICAL JOURNAL, 2018, 卷号: 131, 期号: 24
作者:  Liu, Chun-Feng;  Wang, Tao;  Zhan, Shu-Qin;  Geng, De-Qin;  Wang, Jian
收藏  |  浏览/下载：12/0  |  提交时间：2019/12/05
The recommendations of Chinese Parkinson's disease and movement disorder society consensus on therapeutic management of Parkinson's disease 期刊论文
TRANSLATIONAL NEURODEGENERATION, 2016, 卷号: 5
作者:  Chen, Shengdi;  Chan, Piu;  Sun, Shenggang;  Chen, Haibo;  Zhang, Baorong
收藏  |  浏览/下载：64/0  |  提交时间：2019/12/05
NIPA2 mutations are correlative with childhood absence epilepsy in the Han Chinese population 期刊论文
HUMAN GENETICS, 2014, 卷号: 133, 期号: 5
作者:  Jiang, Yuwu;  Zhang, Yuehua;  Zhang, Pingping;  Zhang, Feng;  Xie, Han
收藏  |  浏览/下载：3/0  |  提交时间：2019/12/19
NIPA2 located in 15q11.2 is mutated in patients with childhood absence epilepsy 期刊论文
HUMAN GENETICS, 2012, 卷号: 131, 期号: 7
作者:  Jiang, Yuwu;  Zhang, Yuehua;  Zhang, Pingping;  Sang, Tian;  Zhang, Feng
收藏  |  浏览/下载：3/0  |  提交时间：2019/12/19
Genetic association between low-density lipoprotein receptor-related protein gene polymorphisms and Alzheimer's disease in Chinese Han population 期刊论文
NEUROSCIENCE LETTERS, 2008, 卷号: 444, 期号: 1
作者:  Zhou, Yong-Tao;  Zhang, Zhen-Xin;  Chan, Piu;  He, Xiao-Ming;  Tang, Mou-Ni
收藏  |  浏览/下载：3/0  |  提交时间：2019/12/19

©版权所有 ©2017 CSpace - Powered by CSpace