Atrial fibrillation in cardiac channelopathies.
作者信息
Thejus Jayachandran, Francis Johnson
机构信息
Calicut Medical College, Kerala, India.
出版信息
Indian Pacing Electrophysiol J. 2009 Nov 1;9(6):342-50.
Abstract
摘要
相似文献
1
Atrial fibrillation in cardiac channelopathies.
Indian Pacing Electrophysiol J. 2009 Nov 1;9(6):342-50.
2
Atrial fibrillation in inherited cardiac channelopathies: From mechanisms to management.
Heart Rhythm. 2016 Sep;13(9):1878-84. doi: 10.1016/j.hrthm.2016.06.008. Epub 2016 Jun 9.
3
Atrial Fibrillation in Inherited Channelopathies.
Card Electrophysiol Clin. 2021 Mar;13(1):155-163. doi: 10.1016/j.ccep.2020.10.004. Epub 2021 Jan 8.
4
Clinical Features of Genetic Cardiac Diseases Related to Potassium Channelopathies.
Card Electrophysiol Clin. 2016 Jun;8(2):361-72. doi: 10.1016/j.ccep.2016.02.001.
5
Channelopathies: a new category of diseases causing sudden death.
Herz. 2007 May;32(3):185-91. doi: 10.1007/s00059-007-2976-1.
6
Mechanisms and clinical management of inherited channelopathies: long QT syndrome, Brugada syndrome, catecholaminergic polymorphic ventricular tachycardia, and short QT syndrome.
Heart Rhythm. 2009 Aug;6(8 Suppl):S51-5. doi: 10.1016/j.hrthm.2009.02.009. Epub 2009 Feb 12.
7
Drug-induced fatal arrhythmias: Acquired long QT and Brugada syndromes.
Pharmacol Ther. 2017 Aug;176:48-59. doi: 10.1016/j.pharmthera.2017.05.001. Epub 2017 May 18.
8
The Atrial Phenotype of the Inherited Primary Arrhythmia Syndromes.
Arrhythm Electrophysiol Rev. 2019 Mar;8(1):42-46. doi: 10.15420/aer.2019.4.2.
9
Short QT syndrome and atrial fibrillation caused by mutation in KCNH2.
J Cardiovasc Electrophysiol. 2005 Apr;16(4):394-6. doi: 10.1046/j.1540-8167.2005.40621.x.
10
Management of ventricular arrhythmias in suspected channelopathies.
Circ Arrhythm Electrophysiol. 2015 Feb;8(1):221-31. doi: 10.1161/CIRCEP.114.002321.
引用本文的文献
1
Fibrinaloid Microclots and Atrial Fibrillation.
Biomedicines. 2024 Apr 17;12(4):891. doi: 10.3390/biomedicines12040891.
2
Where There's Smoke, There's Fire? Significance of Atrial Fibrillation in Young Patients.
Clin Cardiol. 2016 Apr;39(4):229-33. doi: 10.1002/clc.22516. Epub 2016 Feb 5.
本文引用的文献
1
Prevention of inappropriate ICD shocks in patients with Brugada syndrome.
Clin Res Cardiol. 2010 Jan;99(1):37-44. doi: 10.1007/s00392-009-0075-4. Epub 2009 Sep 16.
2
New-onset atrial fibrillation as first clinical manifestation of latent Brugada syndrome: prevalence and clinical significance.
Eur Heart J. 2009 Dec;30(24):2985-92. doi: 10.1093/eurheartj/ehp326.
3
Dual-chamber implantable cardioverter defibrillators reduce clinical adverse events related to atrial fibrillation when compared with single-chamber defibrillators: a subanalysis of the DATAS trial.
Europace. 2009 May;11(5):587-93. doi: 10.1093/europace/eup072.
4
Novel KCNA5 loss-of-function mutations responsible for atrial fibrillation.
J Hum Genet. 2009 May;54(5):277-83. doi: 10.1038/jhg.2009.26. Epub 2009 Apr 3.
5
Predictors of atrial tachyarrhythmias in subjects with type 1 ECG pattern of Brugada syndrome.
Pacing Clin Electrophysiol. 2009 Apr;32(4):500-5. doi: 10.1111/j.1540-8159.2009.02311.x.
6
Remote implantable cardioverter defibrillator monitoring in a Brugada syndrome population.
Europace. 2009 Apr;11(4):489-94. doi: 10.1093/europace/eup034. Epub 2009 Feb 14.
7
Genetics of atrial fibrillation.
Cardiol Clin. 2009 Feb;27(1):25-33, vii. doi: 10.1016/j.ccl.2008.09.007.
8
Atrial Arrhythmias in long-QT syndrome under daily life conditions: a nested case control study.
J Cardiovasc Electrophysiol. 2009 Apr;20(4):401-7. doi: 10.1111/j.1540-8167.2008.01339.x. Epub 2008 Oct 27.
9
A mutation in the sodium channel is responsible for the association of long QT syndrome and familial atrial fibrillation.
Heart Rhythm. 2008 Oct;5(10):1434-40. doi: 10.1016/j.hrthm.2008.07.013. Epub 2008 Jul 19.
10
Molecular genetics of atrial fibrillation.
J Am Coll Cardiol. 2008 Jul 22;52(4):241-50. doi: 10.1016/j.jacc.2008.02.072.
Zotero 插件