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科研机构
暨南大学 [3]
华南理工大学 [2]
中国医学科学院 北京... [2]
内容类型
期刊论文 [4]
会议 [2]
会议论文 [1]
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2019 [1]
2018 [1]
2017 [2]
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Inadvertent transseptal puncture into the aortic root: the narrow edge between luck and catastrophe in interventional cardiology
期刊论文
2019, 卷号: 21, 期号: 7, 页码: 1106-1115
作者:
Chen Hao
;
Fink Thomas
收藏
  |  
浏览/下载:7/0
  |  
提交时间:2020/01/03
Aorta
Cardiac tamponade
Catheter ablation
Complication
Transseptal catheterization
Transseptal puncture
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
Whole Genome Sequence Identified a Rare Homozygous Pathogenic Mutation of the DSG2 Gene in a Familial Arrhythmogenic Cardiomyopathy Involving Both Ventricles
期刊论文
2017, 卷号: 138, 期号: 1, 页码: 41
作者:
Lin, Yubi[1,2]
;
Zhang, Qianhuan[1]
;
Zhong, Zhi An[1]
;
Xu, Zhe[3]
;
He, Siqi[1,2]
收藏
  |  
浏览/下载:17/0
  |  
提交时间:2019/12/06
Experimental, Pathologic, and Clinical Findings of Radiofrequency Catheter Ablation of Para-Hisian Region From the Right Ventricle in Dogs and Humans
期刊论文
2017, 卷号: 10, 期号: 6
作者:
Xue Yumei
;
Zhan Xianzhang
;
Wu Shulin
;
Wang Hongyue
;
Liu Yang
收藏
  |  
浏览/下载:3/0
  |  
提交时间:2020/01/04
arrhythmias
cardiac
bundle of His
catheter ablation
heart ventricles
tachycardia
supraventricular
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
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
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
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