Suppression of atrial fibrillation with mexiletine pharmacotherapy in a young woman with type 1 long QT syndrome
Author:
Publisher
Elsevier BV
Subject
Physiology (medical),Cardiology and Cardiovascular Medicine
Reference17 articles.
1. Cardiac channelopathies: it’s in the genes;Ackerman;Nat Med,2004
2. Effect of clinical phenotype on yield of long QT syndrome genetic testing;Tester;J Am Coll Cardiol,2006
3. A patient with “atrial torsades de pointes.”;Kirchhof;J Cardiovasc Electrophysiol,2000
4. Prolonged atrial action potential durations and polymorphic atrial tachyarrhythmias in patients with long QT syndrome;Kirchhof;J Cardiovasc Electrophysiol,2003
5. Cesium-induced atrial tachycardia degenerating into atrial fibrillation in dogs: atrial torsades de pointes?;Satoh;J Cardiovasc Electrophysiol,1998
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1. Clinical presentation and genetic characterization of early‐onset atrial fibrillation in patients affected by long QT syndrome: A single‐center experience;Journal of Cardiovascular Electrophysiology;2024-07-31
2. Mexiletine: Antiarrhythmic mechanisms, emerging clinical applications and mortality;Pacing and Clinical Electrophysiology;2023-10-17
3. Disease Modelling and Precision Medicine Using Canadian Cardiomyocytes;Canadian Journal of Cardiology;2020-04
4. Action potential shortening rescues atrial calcium alternans;The Journal of Physiology;2018-12-05
5. Atrial fibrillation in young patients;Expert Review of Cardiovascular Therapy;2018-07-02
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