Absence of ECG task force criteria does not rule out structural changes in genotype positive ARVC patients.

[1]  Karim Taha,et al.  The Prognostic Value of Right Ventricular Deformation Imaging in Early Arrhythmogenic Right Ventricular Cardiomyopathy. , 2019, JACC. Cardiovascular imaging.

[2]  G. Hindricks,et al.  Exercise‐related sudden cardiac death of an American football player with arrhythmogenic right ventricular dysplasia/cardiomyopathy AND sarcoidosis , 2019, Clinical case reports.

[3]  B. Merkely,et al.  Cardiac magnetic resonance based deformation imaging: role of feature tracking in athletes with suspected arrhythmogenic right ventricular cardiomyopathy , 2018, The International Journal of Cardiovascular Imaging.

[4]  H. Calkins,et al.  Risk Stratification in Arrhythmogenic Right Ventricular Cardiomyopathy , 2017, Circulation.

[5]  Thor Edvardsen,et al.  Combination of ECG and Echocardiography for Identification of Arrhythmic Events in Early ARVC. , 2017, JACC. Cardiovascular imaging.

[6]  S. Caselli,et al.  RV Remodeling in Olympic Athletes. , 2017, JACC. Cardiovascular imaging.

[7]  Gilbert Habib,et al.  Comprehensive multi-modality imaging approach in arrhythmogenic cardiomyopathy-an expert consensus document of the European Association of Cardiovascular Imaging. , 2017, European heart journal cardiovascular Imaging.

[8]  D. Corrado,et al.  Arrhythmogenic Cardiomyopathy. , 2017, Circulation research.

[9]  E. Behr,et al.  Clinical Differentiation Between Physiological Remodeling and Arrhythmogenic Right Ventricular Cardiomyopathy in Athletes With Marked Electrocardiographic Repolarization Anomalies. , 2015, Journal of the American College of Cardiology.

[10]  Stefan L. Zimmerman,et al.  Clinical Presentation, Long-Term Follow-Up, and Outcomes of 1001 Arrhythmogenic Right Ventricular Dysplasia/Cardiomyopathy Patients and Family Members , 2015, Circulation. Cardiovascular genetics.

[11]  T. Edvardsen,et al.  Vigorous physical activity impairs myocardial function in patients with arrhythmogenic right ventricular cardiomyopathy and in mutation positive family members , 2014, European journal of heart failure.

[12]  Stefan L. Zimmerman,et al.  Yield of serial evaluation in at-risk family members of patients with ARVD/C. , 2014, Journal of the American College of Cardiology.

[13]  J. Svendsen,et al.  The diagnostic performance of imaging methods in ARVC using the 2010 Task Force criteria. , 2014, European heart journal cardiovascular Imaging.

[14]  D. Oxborough,et al.  Physiological Right Ventricular Adaptation in Elite Athletes of African and Afro-Caribbean Origin , 2013, Circulation.

[15]  T. Edvardsen,et al.  Right ventricular mechanical dispersion is related to malignant arrhythmias: a study of patients with arrhythmogenic right ventricular cardiomyopathy and subclinical right ventricular dysfunction. , 2011, European heart journal.

[16]  Wojciech Zareba,et al.  Diagnosis of Arrhythmogenic Right Ventricular Cardiomyopathy/Dysplasia: Proposed Modification of the Task Force Criteria , 2010, Circulation.

[17]  P. Syrris,et al.  Role of genetic analysis in the management of patients with arrhythmogenic right ventricular dysplasia/cardiomyopathy. , 2007, Journal of the American College of Cardiology.

[18]  X. Jouven,et al.  Natural History and Risk Stratification of Arrhythmogenic Right Ventricular Dysplasia/Cardiomyopathy , 2004, Circulation.

[19]  D. Corrado,et al.  Right ventricular cardiomyopathy and sudden death in young people. , 1988, The New England journal of medicine.