Role of Mapping and Ablation in Genetic Diseases: Long QT Syndrome and Catecholaminergic Polymorphic Ventricular Tachycardia-Reference-Cited by-同舟云学术

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Role of Mapping and Ablation in Genetic Diseases: Long QT Syndrome and Catecholaminergic Polymorphic Ventricular Tachycardia

Published:2012-12-18 Issue: Volume: Page:644-655
ISSN:
Container-title:Cardiac Mapping
language:
Short-container-title:

Author:

Fowler Steven J.,Chinitz Larry A.,Priori Silvia G.

Publisher

Wiley-Blackwell

Reference88 articles.

1. HRS/EHRA Expert Consensus Statement on the State of Genetic Testing for the Channelopathies and Cardiomyopathies This document was developed as a partnership between the Heart Rhythm Society (HRS) and the European Heart Rhythm Association (EHRA);Ackerman;Heart Rhythm,2011

2. Genetics of sudden death: focus on inherited channelopathies;Cerrone;Eur Heart J,2011

3. Genetic determinants of cardiac (electric) conduction;Priori;Circ Res,2011

4. Basic mechanisms of reentrant arrhythmias;Antzelevitch;Curr Opin Cardiol,2001

5. Transmural dispersion of repolarization and the T wave;Antzelevitch;Cardiovasc Res,2001

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