Late potentials and ventricular arrhythmias in arrhythmogenic right ventricular cardiomyopathy.

[1]  W. Mckenna,et al.  Gene for arrhythmogenic right ventricular cardiomyopathy with diffuse nonepidermolytic palmoplantar keratoderma and woolly hair (Naxos disease) maps to 17q21. , 1998, Circulation.

[2]  P. Bevilacqua,et al.  Ventricular late potentials, interstitial fibrosis, and right ventricular function in patients with ventricular tachycardia and normal left ventricular function. , 1998, The American journal of cardiology.

[3]  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.

[4]  G. Danieli,et al.  ARVD4, a new locus for arrhythmogenic right ventricular cardiomyopathy, maps to chromosome 2 long arm. , 1997, Genomics.

[5]  M. Goldman,et al.  Value of quantitative measurement of signal-averaged electrocardiographic variables in arrhythmogenic right ventricular dysplasia: correlation with echocardiographic right ventricular cavity dimensions. , 1996, Journal of the American College of Cardiology.

[6]  A. Angelini,et al.  Arrhythmogenic right ventricular cardiomyopathy. Dysplasia, dystrophy, or myocarditis? , 1996, Circulation.

[7]  A. Angelini,et al.  Endomyocardial biopsy in arrhythmogenic right ventricular cardiomyopathy. , 1996, American heart journal.

[8]  B Maisch,et al.  Report of the 1995 World Health Organization/International Society and Federation of Cardiology Task Force on the Definition and Classification of cardiomyopathies. , 1996, Circulation.

[9]  L. Mestroni,et al.  A new locus for arrhythmogenic right ventricular dysplasia on the long arm of chromosome 14. , 1996, Genomics.

[10]  G. Danieli,et al.  A new locus for arrhythmogenic right ventricular cardiomyopathy (ARVD2) maps to chromosome 1q42-q43. , 1995, Human molecular genetics.

[11]  G Thiene,et al.  Arrhythmogenic right ventricular cardiomyopathy in young versus adult patients: similarities and differences. , 1995, Journal of the American College of Cardiology.

[12]  K. Bailey,et al.  Failure of signal-averaged electrocardiography with use of time-domain variables to predict inducible ventricular tachycardia in patients with conduction defects. , 1995, Mayo Clinic proceedings.

[13]  R. Frank,et al.  Time- and Frequency-Domain Analyses of the Signal-Averaged ECG in Patients With Arrhythmogenic Right Ventricular Dysplasia , 1995 .

[14]  G Thiene,et al.  The gene for arrhythmogenic right ventricular cardiomyopathy maps to chromosome 14q23-q24. , 1994, Human molecular genetics.

[15]  M. Kienzle,et al.  Signal‐Averaged ECG Parameters in Cardiac Normals Using Frank Lead System and Fourier Transform Filter and Gender Specific Differences: A Multicenter Study , 1994, Pacing and clinical electrophysiology : PACE.

[16]  A. Nava,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.

[17]  G. Breithardt,et al.  Regional Myocardial Sympathetic Dysinnervation in Arrhythmogenic Right Ventricular Cardiomyopathy: An Analysis Using 123I‐Meta‐Iodobenzylguanidine Scintigraphy , 1994, Circulation.

[18]  P. Coumel,et al.  Late potentials in arrhythmogenic right ventricular dysplasia. Prevalence, diagnostic and prognostic values. , 1993, European heart journal.

[19]  G. Thiene,et al.  Endomyocardial biopsy in right ventricular cardiomyopathy. , 1993, International journal of cardiology.

[20]  W K Haisty,et al.  Establishment of signal-averaged electrocardiographic criteria with Frank XYZ leads and spectral filter used alone and in combination with ejection fraction to predict inducible ventricular tachycardia in coronary artery disease. , 1992, The American journal of cardiology.

[21]  D. Corrado,et al.  Sudden death in young competitive athletes: clinicopathologic correlations in 22 cases. , 1990, The American journal of medicine.

[22]  G. Thiene,et al.  Diagnostic accuracy of right ventriculography in arrhythmogenic right ventricular cardiomyopathy. , 1990, The American journal of cardiology.

[23]  W. Mckenna,et al.  Significance of signal-averaged electrocardiography in relation to endomyocardial biopsy and ventricular stimulation studies in patients with ventricular tachycardia without clinically apparent heart disease. , 1989, Journal of the American College of Cardiology.

[24]  G. Thiene,et al.  Familial occurrence of right ventricular dysplasia: a study involving nine families. , 1988, Journal of the American College of Cardiology.

[25]  S. Olsson,et al.  Quantitative analysis of the signal-averaged QRS in patients with arrhythmogenic right ventricular dysplasia. , 1988, European heart journal.

[26]  M. Laurent,et al.  Critical analysis of cineangiographic criteria for diagnosis of arrhythmogenic right ventricular dysplasia. , 1988, American heart journal.

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

[28]  Y. Biron,et al.  Familial form of arrhythmogenic right ventricular dysplasia. , 1987, American heart journal.

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

[30]  Y. Ozawa,et al.  Detection of late potentials. Comparison of two commercial high-resolution ECG systems. , 1992, Journal of electrocardiology.