Clinical Presentation, Long-Term Follow-Up, and Outcomes of 1001 Arrhythmogenic Right Ventricular Dysplasia/Cardiomyopathy Patients and Family Members.

JA, Groeneweg; A, Bhonsale; CA, James; Riele AS, te; D, Dooijes; C, Tichnell; B, Murray; AC, Wiesfeld; AC, Sawant; B, Kassamali; DE, Atsma; PG, Volders; Groot NM, de; Boer K, de; SL, Zimmerman; IR, Kamel; der Heijden JF, van; SD, Russell; Cramer M, Jan; RJ, Tedford; PA, Doevendans; Veen TA, van; H, Tandri; AA, Wilde; DP, Judge; Tintelen JP, van; RN, Hauer; H, Calkins

doi:10.1161/circgenetics.114.001003

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Clinical Presentation, Long-Term Follow-Up, and Outcomes of 1001 Arrhythmogenic Right Ventricular Dysplasia/Cardiomyopathy Patients and Family Members.

Shared by NobleBlocks on Mar 27, 2015 • 12:00 AM UTC

Authors:

Groeneweg JA

Bhonsale A

James CA

Abstract

<h4>Background</h4>Arrhythmogenic right ventricular dysplasia/cardiomyopathy (ARVD/C) is a progressive cardiomyopathy. We aimed to define long-term outcome in a transatlantic cohort of 1001 individuals.<h4>Methods and results</h4>Clinical and genetic characteristics and follow-up data of ARVD/C inde...

Subject

Genetics

Arrhythmogenic right ventricular dysplasia

Arrhythmias

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