Current perspectives of sudden cardiac death management in hypertrophic cardiomyopathy
Author:
Publisher
Springer Science and Business Media LLC
Subject
Cardiology and Cardiovascular Medicine
Link
https://link.springer.com/content/pdf/10.1007/s10741-023-10355-w.pdf
Reference65 articles.
1. Semsarian C, Ingles J, Maron MS, Maron BJ (2015) New perspectives on the prevalence of hypertrophic cardiomyopathy. J Am Coll Cardiol 65(12):1249–1254. https://doi.org/10.1016/j.jacc.2015.01.019
2. Nishimura RA, Ommen SR, Tajik AJ (2003) Cardiology patient page. Hypertrophic cardiomyopathy: a patient perspective Circulation 108(19):e133–e135
3. Maron BJ, Rowin EJ, Maron MS (2018) Global burden of hypertrophic cardiomyopathy. JACC Heart Fail 6(5):376–378. https://doi.org/10.1016/j.jchf.2018.03.004
4. Maron BJ, Rowin EJ, Casey SA, Maron MS (2016) How hypertrophic cardiomyopathy became a contemporary treatable genetic disease with low mortality: shaped by 50 years of clinical research and practice. JAMA Cardiol 1(1). https://doi.org/10.1001/jamacardio.2015.0354
5. Park YM (2023) Updated risk assessments for sudden cardiac death in hypertrophic cardiomyopathy patients with implantable cardioverter-defibrillator. Korean J Intern Med 38(1). https://doi.org/10.3904/kjim.2022.144
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