Patient’s Guide to Arrhythmogenic Right Ventricular Dysplasia/Cardiomyopathy
Author:
Affiliation:
1. From the Division of Cardiology, Johns Hopkins University School of Medicine, Baltimore, MD (C.T., C.A.J., B.M., H.T., H.C.); and Departments of Psychology and Cardiovascular Sciences, East Carolina University, Greenville, NC (S.F.S.).
Publisher
Ovid Technologies (Wolters Kluwer Health)
Subject
Physiology (medical),Cardiology and Cardiovascular Medicine
Link
https://www.ahajournals.org/doi/pdf/10.1161/CIRCULATIONAHA.113.004845
Reference14 articles.
1. Mutation-Positive Arrhythmogenic Right Ventricular Dysplasia/Cardiomyopathy: The Triangle of Dysplasia Displaced
2. Arrhythmogenic Cardiomyopathy
3. The Cardiac Desmosome and Arrhythmogenic Cardiomyopathies
4. 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)
5. Diagnosis of arrhythmogenic right ventricular cardiomyopathy/dysplasia: Proposed Modification of the Task Force Criteria
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1. Sudden sustained monomorphic ventricular tachycardia in a previously healthy adult with many causes for it, but which one is the correct? A case report;Vojnosanitetski pregled;2023
2. Quality of life metrics in arrhythmogenic right ventricular cardiomyopathy patients: The impact of age, shock and sex;International Journal of Cardiology;2017-12
3. Feasibility of an Assessment Tool for Children’s Competence to Consent to Predictive Genetic Testing: a Pilot Study;Journal of Genetic Counseling;2015-04-26
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