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O’Donnell, D., Cox, D., Bourke, J., et al. (2003) Clinical and electrophysiological differences between patients with arrhythmogenic right ventricular dysplasia and right ventricular outflow tract tachycardia. European Heart Journal, 24, 801-810.
http://dx.doi.org/10.1016/S0195-668X(02)00654-1

has been cited by the following article:

• TITLE: Arrhythmogenic right ventricular cardiomyopathy associated ventricular tachycardia misdiagnosed as idiopathic right ventricular outflow tract origin and its management

  AUTHORS: Xiangmin Shi, Yutang Wang, Zhaoliang Shan

  KEYWORDS: Arrhythmogenic Right Ventricular Cardiomyopathy; Ventricular Tachycardia; Cardiac Magnetic Resonance Imaging

  JOURNAL NAME: Case Reports in Clinical Medicine, Vol.2 No.8, November 6, 2013

  ABSTRACT: Arrhythmogenic right ventricular cardiomyopathy/dysplasia (ARVC/D) is an autosomal dominant genetic form of cardiomyopathy (CM), which primarily affects the right ventricle (RV) and results in life threatening ventricular arrhythmias and sudden cardiac death (SCD). Diagnosis is difficult due to the broad spectrum of phenoltypic variations, especially in the early stage. Clinical suspicion should be raised in the setting of refractory ventricular tachycardia originating from the RV, and the final diagnosis could be made based on the combination of electrocardiography, echocardiography, cardiac magnetic resonance imaging (CMRI) and myocardial biopsy. Implantable cardioverter-defibrillator (ICD) implantation is an effective option for the treatment of ARVC.