Expanding the Spectrum of Arrhythmogenic Cardiomyopathy

Journal of the American College of Cardiology

Volumn 52, Issue 25, 2008, Pages 2188-2189

  Saffitz, Jeffrey E ^a  

^a BETH ISRAEL DEACONESS MEDICAL CENTER   (United States)

Author keywords

arrhythmia; cardiomyopathy; genetics; magnetic resonance imaging; sudden death

Indexed keywords

DESMOPLAKIN;

ARRHYTHMOGENESIS; CARDIOMYOPATHY; CLINICAL FEATURE; DESMOSOME; EDITORIAL; FAMILY HISTORY; GENE MUTATION; GENETIC ANALYSIS; HEART MUSCLE FIBROSIS; HEART RIGHT VENTRICLE DYSPLASIA; HUMAN; LEFT DOMINANT ARRHYTHMOGENIC CARDIOMYOPATHY; PHENOTYPE; PRIORITY JOURNAL;

ARRHYTHMIAS, CARDIAC; CARDIOMYOPATHIES; DEATH, SUDDEN, CARDIAC; ELECTROCARDIOGRAPHY; HUMANS; MAGNETIC RESONANCE IMAGING; VENTRICULAR DYSFUNCTION, LEFT;

EID: 57449117687     PISSN: 07351097     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.jacc.2008.08.062     Document Type: Editorial

References (5)

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2. Thiene G., Nava A., Corrado D., et al. Right ventricular cardiomyopathy and sudden death in young people. N Engl J Med 318 (1988) 129-133
3. Corrado D., Basso C., Thiene G., et al. Spectrum of clinicopathologic manifestations of arrhythmogenic right ventricular cardiomyopathy/dysplasia: a multicenter study. J Am Coll Cardiol 30 (1997) 1512-1520
4. Sen-Chowdhry S., Syrris P., and McKenna W.J. Genetics of right ventricular cardiomyopathy. J Cardiovasc Electrophysio 16 (2005) 927-935
5. Sen-Chowdhry S., Syrris P., Prasad S.K., et al. Left-dominant arrhythmogenic cardiomyopathy: an under-recognized clinical entity. J Am Coll Cardiol 52 (2008) 2175-2187