Zobrazeno 1 - 10
of 307
pro vyhledávání: '"Familial atrial fibrillation"'
Publikováno v:
Frontiers in Cardiovascular Medicine, Vol 7 (2020)
Atrial fibrillation (AF) is the most common clinical tachyarrhythmia. In Europe, AF is expected to reach a prevalence of 18 million by 2060. This estimate will increase hospitalization for AF to 4 million and 120 million outpatient visits. Besides be
Externí odkaz:
https://doaj.org/article/fe760a0cc8db45e8b1ba85e47e22bacc
Autor:
Maen D. Abou Ziki, Johny Michel Abboud, Neha Bhat, Arpita Neogi, Arya Mani, Nelson Ugwu, Ya Liu, Tristan P. Driscoll, Emily Smith, Martin A. Schwartz, Joseph G. Akar, Salah Chouairi
Publikováno v:
Hum Mutat
The genetic causes of atrial fibrillation (AF) with slow conduction are unknown. Eight kindreds with familial AF and slow conduction, including a family affected by early onset AF, heart block and incompletely penetrant non-ischemic dilated cardiomyo
Autor:
Willy G. Ye, Yan-Jie Li, Yi-Qing Yang, Honghong Chen, Ying-Jia Xu, Xing-Biao Qiu, Ruo-Gu Li, Donglin Bai
Publikováno v:
Heart Rhythm. 18:684-693
Background Atrial fibrillation (AF) represents the most common clinical cardiac arrhythmia and substantially increases the risk of cerebral stroke, heart failure, and death. Although causative genes for AF have been identified, the genetic determinan
Autor:
Seock Won Youn, Brandon Chalazan, Liang Hong, Sang-Ging Ong, Hanna Chen, Joseph C. Wu, Mark Maienschein-Cline, Leo Feferman, Olivia T Ly, Jalees Rehman, Meihong Zhang, Dawood Darbar, Erin Lambers, Arvind Sridhar
Publikováno v:
Stem Cell Reports
Summary Mutations in SCN5A, encoding the cardiac sodium channel, are linked with familial atrial fibrillation (AF) but the underlying pathophysiologic mechanisms and implications for therapy remain unclear. To characterize the pathogenesis of AF-link
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Publikováno v:
International Journal of Cardiology. 314:70-74
There is paucity of information on clinical characteristics and outcome of patients with familial atrial fibrillation (AF). The present study was aimed to compare clinical profile and outcome of familial AF with those of non-familial AF.Between Febru
Autor:
Giulia, Guerri, Geraldo, Krasi, Vincenza, Precone, Stefano, Paolacci, Pietro, Chiurazzi, Luca, Arrigoni, Bernardo, Cortese, Astrit, Dautaj, Matteo, Bertelli
Publikováno v:
Acta Bio Medica : Atenei Parmensis
Defects in cardiac electric impulse formation or conduction can lead to an irregular beat (arrhythmia) that can cause sudden death without any apparent cause or after stress. In the following sections, we describe the genetic disorders associated wit
Autor:
Johnson Francis, Jayachandran Thejus
Publikováno v:
Indian Pacing and Electrophysiology Journal, Vol 9, Iss 6, Pp 342-350 (2009)
Atrial fibrillation is the commonest arrhythmia encountered in day-to-day clinical practice. Its prevalence is increasing due to increasing age of the population, increasing prevalence of chronic heart disease and better diagnostic techniques. It is
Externí odkaz:
https://doaj.org/article/d821b3771a024c1b8917bb96629ecfa1
Publikováno v:
Indian Pacing and Electrophysiology Journal, Vol 8, Iss 2, Pp 141-145 (2008)
Percutenous catheter ablation of the accessory pathway in Wolff-Parkinson-White syndrome is a highly successful mode of therapy. Sudden cardiac arrest survivors associated with WPW syndrome should undergo radiofrequency catheter ablation. WPW syndrom
Externí odkaz:
https://doaj.org/article/6b4cb2c1ea87460f940d1ff1fadd0959
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