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Journal of the American College of Cardiology|October 24, 2002
Prospective evaluation of relatives for familial arrhythmogenic right ventricular cardiomyopathy/dysplasia reveals a need to broaden diagnostic criteriaM Shoaib Hamid, Mark Norman, Asifa Quraishi, et al.Circulation|May 25, 2011
Familial evaluation in arrhythmogenic right ventricular cardiomyopathy: impact of genetics and revised task force criteriaGiovanni Quarta, Alison Muir, Antonios Pantazis, et al.Journal of the American College of Cardiology|July 21, 2004
Progressive left ventricular remodeling in patients with hypertrophic cardiomyopathy and severe left ventricular hypertrophyRajesh Thaman, Juan R Gimeno, Sebastian Reith, et al.Molecular Genetics and Metabolism|January 27, 2007
Mutations in PDLIM3 and MYOZ1 encoding myocyte Z line proteins are infrequently found in idiopathic dilated cardiomyopathyAnita M Arola, Ximena Sanchez, Ross T Murphy, et al.Molecular Genetics and Metabolism|May 23, 2018
The effect of enzyme replacement therapy on clinical outcomes in paediatric patients with Fabry disease - A systematic literature review by a European panel of expertsMarco Spada, Ralf Baron, Perry M Elliott, et al.European Journal of Heart Failure|November 18, 2017
Long-term outcomes for different surgical strategies to treat left ventricular outflow tract obstruction in hypertrophic cardiomyopathyRichard Collis, Oliver Watkinson, Constantinos O'Mahony, et al.The American Journal of Cardiology|October 9, 2012
Role of serum N-terminal pro-brain natriuretic peptide measurement in diagnosis of cardiac involvement in patients with anderson-fabry diseaseCaroline J Coats, Valentina Parisi, Monica Ramos, et al.Journal of the American College of Cardiology|February 2, 2002
Immunohistologic evidence of myocardial disease in apparently healthy relatives of patients with dilated cardiomyopathyNiall G Mahon, Brendan P Madden, Alida L P Caforio, et al.European Journal of Heart Failure|April 29, 2021
Expert consensus on the monitoring of transthyretin amyloid cardiomyopathyPablo Garcia-Pavia, Frank Bengel, Dulce Brito, et al.JACC. Heart Failure|July 15, 2019
Screening for Transthyretin Amyloid Cardiomyopathy in Everyday PracticeRonald M Witteles, Sabahat Bokhari, Thibaud Damy, et al.Pageof 24