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Case report of familial sudden cardiac death caused by a DSG2 p.F531C mutation as genetic background when carrying with heterozygous KCNE5 p.D92E/E93X mutation 期刊论文
2018, 卷号: 19
作者:  Lin, Yubi[1,2];  Huang, Jiana[1,3];  He, Siqi[1,3];  Feng, Ruiling[1,3];  Zhong, ZhiAn[2]
收藏  |  浏览/下载:6/0  |  提交时间:2019/12/17
Digoxin-induced anemia among patients with atrial fibrillation and heart failure: clinical data analysis and drug-gene interaction network 期刊论文
ONCOTARGET, 2017, 卷号: 8, 页码: 57003-57011
作者:  Lin, Yubi[1,2,3];  He, Siqi[1,2,3];  Feng, Ruiling[1,2,3];  Xu, Zhe[4];  Chen, Wanqun[5]
收藏  |  浏览/下载:4/0  |  提交时间:2019/04/24
Digoxin-induced anemia among patients with atrial fibrillation and heart failure: clinical data analysis and drug-gene interaction network 期刊论文
2017, 卷号: 8, 期号: 34, 页码: 57003
作者:  Lin, Yubi[1,2,3];  He, Siqi[1,2,3];  Feng, Ruiling[1,2,3];  Xu, Zhe[4];  Chen, Wanqun[5]
收藏  |  浏览/下载:10/0  |  提交时间:2019/12/06
Digoxin-induced Anemia among Patients with Atrial Fibrillation and Heart Failure: Clinical Data Analysis and Drug-gene Interaction Network (CPCI-S收录) 会议
作者:  Lin, Yubi[1,2,3,4,5,6];  Xue, Yumei[1,2,3,4,5];  He, Siqi[1,2,3,4,5,6];  Feng, Ruiling[1,2,3,4,5,6];  Xu, Zhe[7]
收藏  |  浏览/下载:1/0  |  提交时间:2019/04/11
Familial Sudden Cardiac Death Caused by DSG2 Mutation as Genetic Backgrounds: Whole Exome Sequencing and Valid Therapy of Catheter Ablation (CPCI-S收录) 会议
作者:  Lin, Yubi[1,2,3,4,5,6,7];  Zhang, Qianhuan[1,2,3,4,5,6];  Chen, Jia[8];  Feng, Ruiling[1,2,3,4,5,6,7];  He, Siqi[1,2,3,4,5,6,7]
收藏  |  浏览/下载:8/0  |  提交时间:2019/04/11
Whole Exome Sequencing Identified a Pathogenic Mutation in RYR2 in a Chinese Family with Unexplained Sudden Death (CPCI-S收录) 会议
作者:  Lin, Yubi[1,2,3,4,5,6];  Liao, Zili[1,2,3,4,5];  He, Siqi[1,2,3,4,5,6];  Liu, Ruilin[7];  Peng, Yongzheng[8]
收藏  |  浏览/下载:2/0  |  提交时间:2019/04/11
SCN5A Mutants Associated with Familial Cardiac Sodium Overlap Syndrome Characterized as Sick Sinus Syndrome, Atrial Fibrillation, Brugada Syn (CPCI-S收录) 会议
作者:  Lin, Yubi[1,2];  Deng, Chunyu[1,2];  Zhan, XianZhang[1,2];  Xu, Zhe[3];  Zhu, Jiening[1,2]
收藏  |  浏览/下载:11/0  |  提交时间:2019/04/11
Whole Exome Sequencing Identified a Pathogenic Mutation in RYR2 in a Chinese Family with Unexplained Sudden Death 会议论文
Beijing, PEOPLES R CHINA, OCT 12-15, 2017
作者:  Lin, Yubi[1,2,3,4,5,6];  Liao, Zili[1,2,3,4,5];  He, Siqi[1,2,3,4,5,6];  Liu, Ruilin[7];  Peng, Yongzheng[8]
收藏  |  浏览/下载:7/0  |  提交时间:2019/12/13
SCN5A Mutants Associated with Familial Cardiac Sodium Overlap Syndrome Characterized as Sick Sinus Syndrome, Atrial Fibrillation, Brugada Syndrome, and Progressive Conduction Disease 会议论文
Beijing, PEOPLES R CHINA, OCT 12-15, 2017
作者:  Lin, Yubi[1,2];  Deng, Chunyu[1,2];  Zhan, XianZhang[1,2];  Xu, Zhe[3];  Zhu, Jiening[1,2]
收藏  |  浏览/下载:13/0  |  提交时间:2019/12/10
Digoxin-induced Anemia among Patients with Atrial Fibrillation and Heart Failure: Clinical Data Analysis and Drug-gene Interaction Network 会议论文
Beijing, PEOPLES R CHINA, OCT 12-15, 2017
作者:  Lin, Yubi[1,2,3,4,5,6];  Xue, Yumei[1,2,3,4,5];  He, Siqi[1,2,3,4,5,6];  Feng, Ruiling[1,2,3,4,5,6];  Xu, Zhe[7]
收藏  |  浏览/下载:6/0  |  提交时间:2019/12/23


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