[1] Ommen SR., Mital S., Burke MA., Day SM., Deswal A., Elliott P., Evanovich LL., Hung J., Joglar JA., Kantor P., et al. 2020 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. J Am Coll Cardiol 2020; 76(25): e159–240. Doi: 10.1016/j.jacc.2020.08.045.
[2] Writing Committee Members., Ommen SR., Ho CY., Asif IM., Balaji S., Burke MA., Day SM., Dearani JA., Epps KC., Evanovich L., et al. 2024 AHA/ACC/AMSSM/HRS/PACES/SCMR Guideline for the Management of Hypertrophic Cardiomyopathy: A Report of the American Heart Association/American College of Cardiology Joint Committee on Clinical Practice Guidelines. J Am Coll Cardiol 2024; 83(23): 2324–405. Doi: 10.1016/j.jacc.2024.02.014.
[3] Elliot P., Zamorano JL., Anastasakis A., Borger MA., Borggrefe M., Cecchi F., Charron P., Hagege AA., Lafont A., Limongelli G., et al. 2014 ESC guidelines on diagnosis and management of hypertrophic cardiomyopathy: The task force for the diagnosis and management of hypertrophic cardiomyopathy of the European Society of Cardiology (ESC). Eur Heart J 2014; 35(39): 2733–79. Doi: 10.1093/eurheartj/ehu284.
[4] Lipshultz SE., Law YM., Asante-Korang A., Austin ED., Dipchand AI., Everitt MD., Hsu DT., Lin KY., Price JF., Wilkinson JD., et al. Cardiomyopathy in Children: Classification and Diagnosis: A Scientific Statement From the American Heart Association. Circulation 2019; 140(1): E9–68. Doi: 10.1161/CIR.0000000000000682.
[5] Bogle C., Colan SD., Miyamoto SD., Choudhry S., Baez-Hernandez N., Brickler MM., Feingold B., Lal AK., Lee TM., Canter CE., et al. Treatment Strategies for Cardiomyopathy in Children: A Scientific Statement From the American Heart Association. Circulation 2023; 148(2): Epub ahead of print. Doi: 10.1161/CIR.0000000000001151.
[6] Gurschenkov A., Andreeva S., Zaitsev V., Khazov P., Ischmukhametov G., Kozyreva A., Sokolnikova P., Moiseeva O., Kostareva A., Gordeev M. Septal Myectomy in Patients with Hypertrophic Cardiomyopathy and Nonclassical Anderson-Fabry Disease. J Cardiovasc Dev Dis 2024; 11(9): 293. Doi: 10.3390/JCDD11090293.
[7] Colan SD., Lipshultz SE., Lowe AM., Sleeper LA., Messere J., Cox GF., Lurie PR., Orav EJ., Towbin JA. Epidemiology and cause-specific outcome of hypertrophic cardiomyopathy in children: findings from the Pediatric Cardiomyopathy Registry. Circulation 2007; 115(6): 773–81. Doi: 10.1161/CIRCULATIONAHA.106.621185.
[8] Monda E., Rubino M., Lioncino M., Di Fraia F., Pacileo R., Verrillo F., Cirillo A., Caiazza M., Fusco A., Esposito A., et al. Hypertrophic Cardiomyopathy in Children: Pathophysiology, Diagnosis, and Treatment of Non-sarcomeric Causes. Front Pediatr 2021; 9: 632293. Doi: 10.3389/FPED.2021.632293.
[9] Фетисова СГ., Мельник ОВ., Фомичева ЮВ., Сокольникова ПС., Аббясова ВГ., Федорова ОВ., Костарева АА., Васичкина ЕС. Сравнительная информативность применения различных таргетных панелей при генетической диагностике гипертрофической кардиопатии у детей. Трансляционная Медицина 2025; 12(1): 6–14.
[10] Limongelli G., Adorisio R., Baggio C., Bauce B., Biagini E., Castelletti S., Favilli S., Imazio M., Lioncino M., Merlo M., et al. Diagnosis and Management of Rare Cardiomyopathies in Adult and Paediatric Patients. A Position Paper of the Italian Society of Cardiology (SIC) and Italian Society of Paediatric Cardiology (SICP). Int J Cardiol 2022; 357: 55–71. Doi: 10.1016/J.IJCARD.2022.03.050.
[11] Alfares AA., Kelly MA., McDermott G., Funke BH., Lebo MS., Baxter SB., Shen J., McLaughlin HM., Clark EH., Babb LJ., et al. Results of clinical genetic testing of 2,912 probands with hypertrophic cardiomyopathy: Expanded panels offer limited additional sensitivity. Genet Med 2015; 17(11): 880–8. Doi: 10.1038/gim.2014.205.
[12] Ingles J., Sarina T., Yeates L., Hunt L., Macciocca I., Mccormack L., Winship I., Mcgaughran J., Atherton J., Semsarian C. Clinical predictors of genetic testing outcomes in hypertrophic cardiomyopathy. Genet Med 2013; 15(12): 972–7. Doi: 10.1038/GIM.2013.44.
[13] Geisterfer-Lowrance AAT., Kass S., Tanigawa G., Vosberg HP., McKenna W., Seidman CE., Seidman JG. A molecular basis for familial hypertrophic cardiomyopathy: a beta cardiac myosin heavy chain gene missense mutation. Cell 1990; 62(5): 999–1006. Doi: 10.1016/0092-8674(90)90274-I.
[14] Seidman JG., Seidman C. The genetic basis for cardiomyopathy: from mutation identification to mechanistic paradigms. Cell 2001; 104(4): 557–67. Doi: 10.1016/S0092-8674(01)00242-2.
[15] Seidman CE., Seidman JG. Identifying sarcomere gene mutations in hypertrophic cardiomyopathy: a personal history. Circ Res 2011; 108(6): 743–50. Doi: 10.1161/CIRCRESAHA.110.223834.
[16] Liew AC., Vassiliou VS., Cooper R., Raphael CE. Hypertrophic Cardiomyopathy-Past, Present and Future. J Clin Med 2017; 6(12): 118. Doi: 10.3390/JCM6120118.
[17] Maron BA., Wang RS., Carnethon MR., Rowin EJ., Loscalzo J., Maron BJ., Maron MS. What Causes Hypertrophic Cardiomyopathy? Am J Cardiol 2022; 179: 74–82. Doi: 10.1016/j.amjcard.2022.06.017.
[18] Maron BJ., Ommen SR., Semsarian C., Spirito P., Olivotto I., Maron MS. Hypertrophic cardiomyopathy: present and future, with translation into contemporary cardiovascular medicine. J Am Coll Cardiol 2014; 64(1): 83–99. Doi: 10.1016/J.JACC.2014.05.003.
[19] Шляхто ЕВ., Семернин ЕН., Гудкова АЯ., Костарева АА. Первичные кардиомиопатии, современное представление. Терапевтический Архив 2005; 77(12): 77–83.
[20] Gersh BJ., Maron BJ., Bonow RO., Dearani JA., Fifer MA., Link MS., Naidu SS., Nishimura RA., Ommen SR., Rakowski H., et al. 2011 ACCF/AHA guideline for the diagnosis and treatment of hypertrophic cardiomyopathy: Executive summary: A report of the American College of cardiology foundation/American heart association task force on practice guidelines. Circulation 2011; 124(24): 2761–96. Doi: 10.1161/CIR.0b013e318223e230.
[21] Kelly MA., Caleshu C., Morales A., Buchan J., Wolf Z., Harrison SM., Cook S., Dillon MW., Garcia J., Haverfield E., et al. Adaptation and validation of the ACMG/AMP variant classification framework for MYH7-associated inherited cardiomyopathies: Recommendations by ClinGen’s Inherited Cardiomyopathy Expert Panel. Genet Med 2018; 20(3): 351–9. Doi: 10.1038/gim.2017.218.