Pathogenetics of Cardiomyopathy
Author:
Publisher
Pleiades Publishing Ltd
Subject
Genetics
Link
https://link.springer.com/content/pdf/10.1134/S1022795423050101.pdf
Reference122 articles.
1. McKenna, W.J., Maron, B.J., and Thiene, G., Classification, epidemiology, and global burden of cardiomyopathies, Circ. Res., 2017, vol. 121, no. 7, pp. 722—730. https://doi.org/10.1161/CIRCRESAHA.117.309711
2. Salemi, V.M.C., Mohty, D., Altavila, S.L.L., et al., Insights into the classification of cardiomyopathies: past, present, and future directions, Clinics (São Paulo), 2021, vol. 76, р. e2808. https://doi.org/10.6061/clinics/2021/e2808
3. McKenna, W.J. and Judge, D.P., Epidemiology of the inherited cardiomyopathies, Nat. Rev. Cardiol., 2021, vol. 18, no. 1, pp. 22—36. https://doi.org/10.1038/s41569-020-0428-2
4. Ommen, S.R., Mital, S., Burke, M.A., et al., AHA/ACC guideline for the diagnosis and treatment of patients with hypertrophic cardiomyopathy: a report of the American College of Cardiology/American Heart Association Joint Committee on Clinical Practice Guidelines, Circulation, 2020, vol. 142, no. 25, рp. e558—e631. https://doi.org/10.1161/CIR.0000000000000937
5. Corrado, D., Link, M.S., and Calkins, H., Arrhythmogenic right ventricular cardiomyopathy, N. Engl. J. Med., 2017, vol. 376, no. 1, pp. 61—72. https://doi.org/10.1056/NEJMra1509267
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