Genetics of Dilated Cardiomyopathy
Author:
Publisher
Springer Science and Business Media LLC
Subject
Cardiology and Cardiovascular Medicine
Link
http://link.springer.com/article/10.1007/s11886-018-1061-0/fulltext.html
Reference38 articles.
1. Richardson P, McKenna W, Bristow M, Maisch B, Mautner B, O’Connell J, et al. Report of the 1995 World Health Organization/International Society and Federation of Cardiology Task Force on the definition and classification of cardiomyopathies. Circulation. 1996;93:841–2.
2. Mestroni L, Brun F, Spezzacatene A, Sinagra G, Taylor MRG. Genetic causes of dilated cardiomyopathy. Prog Pediatr Cardiol. 2014;37:13–8. https://doi.org/10.1016/j.ppedcard.2014.10.003 .
3. •• Bozkurt B, Colvin M, Cook J, Cooper LT, Deswal A, Fonarow GC, et al. Current diagnostic and treatment strategies for specific dilated cardiomyopathies: A scientific statement from the American Heart Association. Circulation. 2016;134:579–646. Doi: https://doi.org/10.1161/CIR.0000000000000455 . A summary of knowledge regarding DCM, emphasizing recent developments in therapeutic approaches for cardiomyopathies.
4. Bashore TM, Granger CB, Jackson KP, Patel MR. Heart disease. In: Papadakis MA, McPhee SJ, Rabow MW, editors. Current Medical Diagnosis & Treatment 2018. New York: McGraw-Hill; 2018.
5. •• Bakalakos A, Risatos K, Anastasakis A. Current perspective on the diagnosis and management of dilated cardiomyopathy Beyond heart failure: a Cardiomyopathy Clinic Doctor’s point of view. Hellenic Journal of Cardiology. 2018. https://doi.org/10.1016/j.hjc/2018.05.008 Provides a comprehensive review of DCM diagnosis and management, including new classification concepts and identified genes by the American Heart Association.
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