Malignant arrhythmogenic right ventricular dysplasia/cardiomyopathy with a normal 12-lead electrocardiogram: a rare but underrecognized clinical entity.

[1]  Stefan L. Zimmerman,et al.  Mutation‐Positive Arrhythmogenic Right Ventricular Dysplasia/Cardiomyopathy: The Triangle of Dysplasia Displaced , 2013, Journal of cardiovascular electrophysiology.

[2]  Stefan L. Zimmerman,et al.  Incremental value of cardiac magnetic resonance imaging in arrhythmic risk stratification of arrhythmogenic right ventricular dysplasia/cardiomyopathy-associated desmosomal mutation carriers. , 2013, Journal of the American College of Cardiology.

[3]  S. Russell,et al.  Risk Stratification in Arrhythmogenic Right Ventricular Dysplasia/Cardiomyopathy–Associated Desmosomal Mutation Carriers , 2012, Circulation. Arrhythmia and electrophysiology.

[4]  Matthew N Peters,et al.  Diagnosis of Arrhythmogenic Right Ventricular Cardiomyopathy , 2012, Proceedings.

[5]  W. Birchmeier,et al.  Sodium current deficit and arrhythmogenesis in a murine model of plakophilin-2 haploinsufficiency. , 2012, Cardiovascular research.

[6]  Michael J Ackerman,et al.  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). , 2011, Europace : European pacing, arrhythmias, and cardiac electrophysiology : journal of the working groups on cardiac pacing, arrhythmias, and cardiac cellular electrophysiology of the European Society of Cardiology.

[7]  H. Calkins,et al.  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). , 2011, Heart rhythm.

[8]  Tachapong Ngarmukos,et al.  Prevention of Ventricular Fibrillation Episodes in Brugada Syndrome by Catheter Ablation Over the Anterior Right Ventricular Outflow Tract Epicardium , 2011, Circulation.

[9]  L. Jordaens,et al.  Arrhythmogenic Right Ventricular Dysplasia/Cardiomyopathy Diagnostic Task Force Criteria: Impact of New Task Force Criteria , 2010, Circulation. Arrhythmia and electrophysiology.

[10]  Mark Potse,et al.  UvA-DARE ( Digital Academic Repository ) Pathophysiological mechanisms of arrhythmogenic right ventricular disorders , 2013 .

[11]  R. Hauer,et al.  New ECG Criteria in Arrhythmogenic Right Ventricular Dysplasia/Cardiomyopathy , 2009, Circulation. Arrhythmia and electrophysiology.

[12]  G. Guerrero-Serna,et al.  Loss of Plakophilin-2 Expression Leads to Decreased Sodium Current and Slower Conduction Velocity in Cultured Cardiac Myocytes , 2009, Circulation Research.

[13]  S. Russell,et al.  Electrocardiographic Features of Arrhythmogenic Right Ventricular Dysplasia , 2009, Circulation.

[14]  H. Calkins,et al.  Arrhythmogenic right ventricular cardiomyopathy/dysplasia clinical presentation and diagnostic evaluation: results from the North American Multidisciplinary Study. , 2009, Heart rhythm.

[15]  C. Vassanelli,et al.  Arrhythmogenic right ventricular dysplasia/cardiomyopathy presenting as ST-segment elevation myocardial infarction: a case report. , 2009, Resuscitation.

[16]  C. Antzelevitch,et al.  Is there an overlap between Brugada syndrome and arrhythmogenic right ventricular cardiomyopathy/dysplasia? , 2005, Journal of electrocardiology.

[17]  S. Russell,et al.  Arrhythmogenic Right Ventricular Dysplasia: A United States Experience , 2005, Circulation.

[18]  S. Peters,et al.  Diagnosis of Arrhythmogenic Right Ventricular Dysplasia‐Cardiomyopathy: Value of Standard ECG Revisited , 2003, Annals of noninvasive electrocardiology : the official journal of the International Society for Holter and Noninvasive Electrocardiology, Inc.

[19]  B. Schnitzler,et al.  Arrêt cardiocirculatoire chez une adolescente et dysplasie arythmogène du ventricule droit , 1998 .

[20]  M. Davies,et al.  Spectrum of clinicopathologic manifestations of arrhythmogenic right ventricular cardiomyopathy/dysplasia: a multicenter study. , 1997, Journal of the American College of Cardiology.

[21]  D. Corrado,et al.  Familial cardiomyopathy underlies syndrome of right bundle branch block, ST segment elevation and sudden death. , 1996, Journal of the American College of Cardiology.

[22]  G. Thiene,et al.  Diagnosis of arrhythmogenic right ventricular dysplasia/cardiomyopathy. Task Force of the Working Group Myocardial and Pericardial Disease of the European Society of Cardiology and of the Scientific Council on Cardiomyopathies of the International Society and Federation of Cardiology. , 1994, British heart journal.

[23]  J. Brugada,et al.  Right bundle branch block, persistent ST segment elevation and sudden cardiac death: a distinct clinical and electrocardiographic syndrome. A multicenter report. , 1992, Journal of the American College of Cardiology.

[24]  R Frank,et al.  Right Ventricular Dysplasia: A Report of 24 Adult Cases , 1982, Circulation.

[25]  A. Waldo.  Activation Delay and VT Parameters in Arrhythmogenic Right Ventricular Dysplasia/Cardiomyopathy: Toward Improvement of Diagnostic ECG Criteria , 2009 .

[26]  M. Boursier,et al.  [Cardiac arrest in an adolescent with arrhythmogenic right ventricular dysplasia]. , 1998, Annales francaises d'anesthesie et de reanimation.