Genetics of Dilated Cardiomyopathy

Author:

Fu Yiwen,Eisen Howard J.

Publisher

Springer Science and Business Media LLC

Subject

Cardiology and Cardiovascular Medicine

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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