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Potential therapeutic effects of and on adenine-induced chronic renal failure in rats and their phytochemical analysis 期刊论文
Drug design, development and therapy, 2019, 卷号: 13, 页码: 103-117
作者:  Li, Ling;  Zhang, Tong;  Li, Chunru;  Xie, Lu;  Li, Ning
收藏  |  浏览/下载:25/0  |  提交时间:2019/01/08
PRRT2 mutations in a cohort of Chinese families with paroxysmal kinesigenic dyskinesia and genotype-phenotype correlation reanalysis in literatures 期刊论文
INTERNATIONAL JOURNAL OF NEUROSCIENCE, 2018, 卷号: 128, 期号: 8, 页码: 751-760
作者:  Zhao, Guohua;  Liu, Xiaomin;  Zhang, Qiong;  Wang, Kang
收藏  |  浏览/下载:3/0  |  提交时间:2019/12/11
Reduced Penetrance of PRRT2 Mutation in a Chinese Family With Infantile Convulsion and Choreoathetosis Syndrome 期刊论文
JOURNAL OF CHILD NEUROLOGY, 2015, 卷号: 30, 期号: 10
作者:  Zhang, L. M.;  An, Y.;  Pan, G.;  Ding, Y. F.;  Zhou, Y. F.
收藏  |  浏览/下载:6/0  |  提交时间:2019/12/19
PRRT2 c.649dupC Mutation Derived from De Novo in Paroxysmal Kinesigenic Dyskinesia 期刊论文
CNS NEUROSCIENCE & THERAPEUTICS, 2013, 卷号: 19, 期号: 1, 页码: 61-65
Li, HF; Ni, W; Xiong, ZQ; Xu, JF; Wu, ZY
收藏  |  浏览/下载:65/0  |  提交时间:2013/06/04
Mutation analysis of PRRT2 in two Chinese BFIS families and nomenclature of PRRT2 related paroxysmal diseases 期刊论文
Neuroscience letters, 2013, 卷号: 552, 页码: 40-45
作者:  Jun-Ling Wang;  Xiao Mao;  Zheng-Mao Hu;  Jia-Da Li;  Nan Li
收藏  |  浏览/下载:12/0  |  提交时间:2019/12/03
Linkage analysis and gene mapping of one Chinese family with benign familial infantile convulsions]. 期刊论文
Chinese journal of contemporary pediatrics, 2010, 卷号: 12, 期号: [db:dc_citation_issue], 页码: 89-92
作者:  Zhou Xi-Hui;  Ma Ai-Qun;  Liu Xiao-Hong;  Huang Chen;  Zhang Yan-Min
收藏  |  浏览/下载:2/0  |  提交时间:2019/12/10
Mutation analysis of WASF2 and GALE genes in one Chinese family with benign familial infantile convulsions with a novel locus (Journal of Investigative Medicine (2007) 55 (439Y443)) 期刊论文
Journal of Investigative Medicine, 2008, 卷号: 55, 期号: 8, 页码: 439-443
作者:  Xiaohong, Zi;  Abuhamed, Mutasem;  Ya-qin, Wang
收藏  |  浏览/下载:6/0  |  提交时间:2019/12/27


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