Multiple clinical profiles of families with the short QT syndrome

Author:

Akdis D1,Saguner A M1,Medeiros-Domingo A2,Schaller A3,Balmer C4,Steffel J1,Brunckhorst C1,Duru F1

Affiliation:

1. Department of Cardiology, University Heart Center Zurich, Rämistrasse 100, CH-8091 Zurich, Switzerland

2. Department of Cardiology, Inselspital Bern, University Hospital Bern, Freiburgstrasse 8, CH-3010 Bern, Switzerland

3. Division of Human Genetics, Department of Pediatrics, Inselspital Bern, University Hospital Bern, Freiburgstrasse 8, CH-3010 Bern, Switzerland

4. Department of Cardiology, University Children's Hospital Zurich, Steinwiesstrasse 75, CH-8032 Zürich, Switzerland

Publisher

Oxford University Press (OUP)

Subject

Physiology (medical),Cardiology and Cardiovascular Medicine

Reference22 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;Europace,2011

2. Long-term follow-up of patients with short QT syndrome;Giustetto;J Am Coll Cardiol,2011

3. Long-term follow-up of a pediatric cohort with short QT syndrome;Villafañe;J Am Coll Cardiol,2013

4. Amplified transmural dispersion of repolarization as the basis for arrhythmogenesis in a canine ventricular-wedge model of short-QT syndrome;Extramiana;Circulation,2004

5. Short QT in a cohort of 1.7 million persons: prevalence, correlates, and prognosis;Iribarren;Ann Noninvasive Electrocardiol,2014

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