Zobrazeno 1 - 10
of 23
pro vyhledávání: '"Ruo‐Min Di"'
Autor:
Jia-Ning Gu, Chen-Xi Yang, Yuan-Yuan Ding, Qi Qiao, Ruo-Min Di, Yu-Min Sun, Jun Wang, Ling Yang, Ying-Jia Xu, Yi-Qing Yang
Publikováno v:
Diagnostics, Vol 13, Iss 2, p 242 (2023)
Dilated cardiomyopathy (DCM), characterized by left ventricular or biventricular enlargement with systolic dysfunction, is the most common type of cardiac muscle disease. It is a major cause of congestive heart failure and the most frequent indicatio
Externí odkaz:
https://doaj.org/article/07d5f866146a4cdda9bd767eb8ee1444
Autor:
Xiao‐Juan Guo, Xing‐Biao Qiu, Jun Wang, Yu‐Han Guo, Chen‐Xi Yang, Li Li, Ri‐Feng Gao, Zun‐Ping Ke, Ruo‐Min Di, Yu‐Min Sun, Ying‐Jia Xu, Yi‐Qing Yang
Publikováno v:
Journal of the American Heart Association: Cardiovascular and Cerebrovascular Disease, Vol 10, Iss 23 (2021)
Background Atrial fibrillation (AF) is the most common form of clinical cardiac dysrhythmia responsible for thromboembolic cerebral stroke, congestive heart failure, and death. Aggregating evidence highlights the strong genetic basis of AF. Neverthel
Externí odkaz:
https://doaj.org/article/43d6be9f7b214966928c21bdd4e668d3
Autor:
Kai-Yue Han, Qi Qiao, Ye-Qian Zhu, Xin-Guang Chen, Xing-Xing Kang, Gao-Feng Zhang, Xun-Chao Cai, Yong Du, Jing Jin, Ruo-Min Di, Chen-Xi Yang, Feng-Xiang Zhang, Ying-Jia Xu
Publikováno v:
Cardiology Research and Practice, Vol 2021 (2021)
The number of confirmed COVID-19 cases has increased drastically; however, information regarding the impact of this disease on the occurrence of arrhythmias is scarce. The aim of this study was to determine the impact of COVID-19 on arrhythmia occurr
Externí odkaz:
https://doaj.org/article/067d880085a14598b397d47b3717fdc4
Autor:
Xinguang Chen, Xing-Xing Kang, Yeqian Zhu, Chen-Xi Yang, Kai-Yue Han, Jing Jin, Qi Qiao, Yong Du, Xun-Chao Cai, Ruo-Min Di, Gao-Feng Zhang, Fengxiang Zhang, Ying-Jia Xu
Publikováno v:
Cardiology Research and Practice
Cardiology Research and Practice, Vol 2021 (2021)
Cardiology Research and Practice, Vol 2021 (2021)
The number of confirmed COVID-19 cases has increased drastically; however, information regarding the impact of this disease on the occurrence of arrhythmias is scarce. The aim of this study was to determine the impact of COVID-19 on arrhythmia occurr
Autor:
Hong-Yu Shi, Meng-Shi Xie, Yu-Han Guo, Chen-Xi Yang, Jia-Ning Gu, Qi Qiao, Ruo-Min Di, Xing-Biao Qiu, Ying-Jia Xu, Yi-Qing Yang
Publikováno v:
European Journal of Medical Genetics. 66:104705
Autor:
Chen-Xi Yang, Xing-Biao Qiu, Ying-Jia Xu, Zun-Ping Ke, Li Li, Xiao-Juan Guo, Yi-Qing Yang, Ri-Feng Gao, Ruo-Min Di, Jun Wang, Yu-Min Sun, Yu-Han Guo
Publikováno v:
Journal of the American Heart Association: Cardiovascular and Cerebrovascular Disease, Vol 10, Iss 23 (2021)
Background Atrial fibrillation (AF) is the most common form of clinical cardiac dysrhythmia responsible for thromboembolic cerebral stroke, congestive heart failure, and death. Aggregating evidence highlights the strong genetic basis of AF. Neverthel
Autor:
Ruo-Min Di, Xing-Biao Qiu, Yi-Qing Yang, Xiu-Mei Li, Ruo-Gu Li, Li Li, Min Zhang, Ying-Jia Xu, Juan Wang, Lan Ma, Xun Li, Qi Qiao
Publikováno v:
Heart and Vessels. 34:658-668
Congenital heart defect (CHD) is the most common form of birth deformity and is responsible for substantial morbidity and mortality in humans. Increasing evidence has convincingly demonstrated that genetic defects play a pivotal role in the pathogene
Autor:
Yi-Qing Yang, Xin-Hua Wang, Ying-Jia Xu, Xing-Biao Qiu, Ruo-Gu Li, Ruo-Min Di, Xiu-Mei Li, Ning Li, Zhang-Sheng Wang, Min Zhang, Qi Qiao, Xiao-Juan Guo
Publikováno v:
International Journal of Medical Sciences
Atrial fibrillation (AF), as the most common sustained cardiac arrhythmia, is associated with substantially increased morbidity and mortality. Aggregating evidence demonstrates that genetic defects play a crucial role in the pathogenesis of AF, espec
Autor:
Ri-Tai Huang, Xiu-Mei Li, Song Xue, Ruo-Min Di, Juan Wang, Xing-Yuan Liu, Qi Qiao, Ying-Jia Xu, Yi-Qing Yang
Publikováno v:
Gene. 663:115-120
Congenital bicuspid aortic valve (BAV), the most common form of birth defect in humans, is associated with substantial morbidity and mortality. Increasing evidence demonstrates that genetic risk factors play a key role in the pathogenesis of BAV. How
Autor:
Chen-Xi Yang, Xiu-Mei Li, Yi-Qing Yang, Jia-Ning Gu, Ruo-Min Di, Fang Yuan, Cui-Mei Zhao, Qi Qiao, Ying-Jia Xu
Publikováno v:
European journal of medical genetics. 63(4)
As a prevalent primary myocardial disease, dilated cardiomyopathy (DCM) represents the most common cause of heart failure in the young and the most frequent indication for cardiac transplantation. Aggregating evidence highlights the genetic basis of