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  1. 1
    Academic Journal

    المساهمون: Not specified., Отсутствует.

    المصدر: Current Pediatrics; Том 23, № 2 (2024); 63-70 ; Вопросы современной педиатрии; Том 23, № 2 (2024); 63-70 ; 1682-5535 ; 1682-5527

    وصف الملف: application/pdf

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JACC Clin Electrophysiol. 2016;2(3):253–262. doi: https://doi.org/10.1016/j.jacep.2016.01.020; Priori SG, Blomstrom-Lundqvist C, Mazzanti A, et al. 2015 ESC Guidelines for the management of patients with ventricular arrhythmias and the prevention of sudden cardiac death the Task Force for the Management of Patients with Ventricular Arrhythmias and the Prevention of Sudden Cardiac Death of the European Society of Cardiology (ESC) Endorsed by: Association for European Paediatric and Congenital Cardiology (AEPC). Eur Heart J. 2015;36(41):2793–867l. doi: https://doi.org/10.1093/eurheartj/ehv316; Ackerman MJ, Priori SG, Dubin AM, et al. Beta-blocker therapy for long QT syndrome and catecholaminergic polymorphic ventricular tachycardia: Are all beta-blockers equivalent? Heart Rhythm. 2017;14(1):e41–e44. doi: https://doi.org/10.1016/j.hrthm.2016.09.012; Leren IS, Saberniak J, Majid E, et al. Nadolol decreases the incidence and severity of ventricular arrhythmias during exercise stress testing compared with β1-selective β-blockers in patients with catecholaminergic polymorphic ventricular tachycardia. Heart Rhythm. 2016;13(2):432–440. doi: https://doi.org/10.1016/j.hrthm.2015.09.029; Peltenburg PJ, Kallas D, Bos JM, et al. An International Multicenter Cohort Study on β-Blockers for the Treatment of Symptomatic Children With Catecholaminergic Polymorphic Ventricular Tachycardia. Circulation. 2022;145(5):333–344. doi: https://doi.org/10.1161/CIRCULATIONAHA.123.064786; Hayashi M, Denjoy I, Extramiana F, et al. Incidence and risk factors of arrhythmic events in catecholaminergic polymorphic ventricular tachycardia. Circulation. 2009;119(18):2426–2434. doi: https://doi.org/10.1161/CIRCULATIONAHA.108.829267; Roston TM, Vinocur JM, Maginot KR, et al. Catecholaminergic Polymorphic Ventricular Tachycardia in Children: Analysis of Therapeutic Strategies and Outcomes from an International Multicenter Registry. Circ Arrhythm Electrophysiol. 2015;8(3):633–642. doi: https://doi.org/10.1161/CIRCEP.114.002217; Sumitomo N, Harada K, Nagashima M, et al. Catecholaminergic polymorphic ventricular tachycardia: Electrocardiographic characteristics and optimal therapeutic strategies to prevent sudden death. Heart. 2003;89(1):66–70. doi: https://doi.org/10.1136/heart.89.1.66; Березницкая В.В., Кульбачинская Е.К., Школьникова М.А. Особенности клинических проявлений и эффективность антиаритмической терапии у больных с катехоламинергической полиморфной желудочковой тахикардией // Вестник аритмологии. — 2021.—Т.28.—№4.—С.62–69.—doi:https://doi.org/10.35336/VA-2021-4-62-69; Кульбачинская Е.К., Березницкая В.В. CASQ2: клинико-генетические особенности катехоламинергической полиморфной желудочковой тахикардии в трех семьях // Альманах клинической медицины. — 2023. — Т. 51. — № 3. — С. 192–199. — doi: https://doi.org/10.18786/2072-0505-2023-51-022; Mazzanti A, Kukavica D, Trancuccio A, et al. Outcomes of Patients With Catecholaminergic Polymorphic Ventricular Tachycardia Treated With β-Blockers. JAMA Cardiol. 2022;7(5):504–512. doi: https://doi.org/10.1001/jamacardio.2022.0219; Veith M, El-Battrawy I, Roterberg G, et al. Long-Term Follow-Up of Patients with Catecholaminergic Polymorphic Ventricular Arrhythmia. J Clin Med. 2020;9(4):903. doi: https://doi.org/10.3390/jcm9040903; Priori SG, Napolitano C, Memmi M, et al. Clinical and molecular characterization of patients with catecholaminergic polymorphic ventricular tachycardia. Circulation. 2002;106(1):69–74. doi: https://doi.org/10.1161/01.cir.0000020013.73106.d8; Marai I, Khoury A, Suleiman M, et al. Importance of ventricular tachycardia storms not terminated by implantable cardioverter defibrillators shocks in patients with CASQ2 associated catecholaminergic polymorphic ventricular tachycardia. Am J Cardiol. 2012;110(1):72–76. doi: https://doi.org/110.1016/j.amjcard.2012.02.049; Kawata H, Ohno S, Aiba T, et al. Catecholaminergic polymorphic ventricular tachycardia (CPVT) associated with ryanodine receptor (RyR2) gene mutations: Long-term prognosis after initiation of medical treatment. Circ J. 2016;80(9):1907–1915. doi: https://doi.org/10.1253/circj.CJ-16-0250; Li Y, Peng X, Lin R, et al. The Antiarrhythmic Mechanisms of Flecainide in Catecholaminergic Polymorphic Ventricular Tachycardia. Front Physiol. 2022;13:850117. doi: https://doi.org/10.3389/fphys.2022.850117; Salvage SC, Huang CL, Fraser JA, Dulhunty AF. How does flecainide impact RyR2 channel function? J Gen Physiol. 2022;154(9): e202213089. doi: https://doi.org/10.1085/jgp.202213089; Bannister ML, MacLeod KT, George CH. Moving in the right direction: elucidating the mechanisms of interaction between flecainide and the cardiac ryanodine receptor. Br J Pharmacol. 2022;179(11):2558–2563. doi: https://doi.org/10.1111/bph.15718; Kryshtal DO, Blackwell DJ, Egly CL, et al. RYR2 Channel Inhibition Is the Principal Mechanism of Flecainide Action in CPVT. Circ Res. 2021;128(3):321–331. doi: https://doi.org/10.1161/CIRCRESAHA.120.316819; Kannankeril PJ, Moore JP, Cerrone M, et al. Efficacy of flecainide in the treatment of catecholaminergic polymorphic ventricular tachycardia a randomized clinical trial. JAMA Cardiology. 2017;2(7):759–766. doi: https://doi.org/10.1001/jamacardio.2017.1320; Khoury A, Marai I, Suleiman M, et al. Flecainide therapy suppresses exercise-induced ventricular arrhythmias in patients with CASQ2-associated catecholaminergic polymorphic ventricular tachycardia. Heart Rhythm. 2013;10(11):1671–1675. doi: https://doi.org/10.1016/j.hrthm.2013.08.011; Watanabe H, Van Der Werf C, Roses-Noguer F, et al. Effects of flecainide on exercise-induced ventricular arrhythmias and recurrences in genotype-negative patients with catecholaminergic polymorphic ventricular tachycardia. Heart Rhythm. 2013;10(4):542–547. doi: https://doi.org/10.1016/j.hrthm.2012.12.035; Jacquemart C, Ould Abderrahmane F, Massin MM. Effects of flecainide therapy on inappropriate shocks and arrhythmias in catecholaminergic polymorphic ventricular tachycardia. J Electrocardiol. 2012;45(6):736–738. doi: https://doi.org/10.1016/j.jelectrocard.2012.05.002; Pott C, Dechering DG, Reinke F, et al. Successful treatment of catecholaminergic polymorphic ventricular tachycardia with flecainide: A case report and review of the current literature. Europace. 2011;13(6):897–901. doi: https://doi.org/10.1093/europace/euq517; Padfield GJ, AlAhmari L, Lieve KV, et al. Flecainide monotherapy is an option for selected patients with catecholaminergic polymorphic ventricular tachycardia intolerant of beta-blockade. Heart Rhythm. 2016;13(2):609–613. doi: https://doi.org/10.1016/j.hrthm.2015.09.027; Savio-Galimberti E, Knollmann BC. Channel activity of cardiac ryanodine receptors (RyR2) determines potency and efficacy of flecainide and R-propafenone against arrhythmogenic calcium waves in ventricular cardiomyocytes. PLoS One. 2015;10(6):e0131179. doi: https://doi.org/10.1371/journal.pone.0131179; Marx A, Lange B, Nalenz C, et al. A 35-year effective treatment of catecholaminergic polymorphic ventricular tachycardia with propafenone. HeartRhythm Case Reports. 2019;5(2):74–77. doi: https://doi.org/10.1016/j.hrcr.2018.04.003; Li S, Lv T, Yang J, et al. A gain of function ryanodine receptor 2 mutation (R1760W-RyR2) in catecholaminergic polymorphic ventricular tachycardia. Clin Exp Pharmacol Physiol. 2023;50(1):39–49. doi: https://doi.org/10.1111/1440-1681.13722; Vaksmann G, Klug D. Efficacy of ivabradine to control ventricular arrhythmias in catecholaminergic polymorphic ventricular tachycardia. Pacing Clin Electrophysiol. 2018;41(10):1378–1380. doi: https://doi.org/10.1111/pace.13446; Kohli U, Aziz Z, Beaser AD, Nayak HM. A large deletion in RYR2 exon 3 is associated with nadolol and flecainide refractory catecholaminergic polymorphic ventricular tachycardia. Pacing Clin Electrophysiol. 2019;42(8):1146–1154. doi: https://doi.org/10.1111/pace.13668; Roston TM, Hart A, Krahn AD, Sanatani S. The challenge of implantable cardioverter-defibrillator programming and shock interpretation in treatment-refractory catecholaminergic polymorphic ventricular tachycardia. J Cardiovasc Med (Hagerstown). 2019;20(8):569–571. doi: https://doi.org/10.2459/JCM.0000000000000814; Miyake CY, Webster G, Czosek RJ, et al. Efficacy of implantable cardioverter defibrillators in young patients with catecholaminergic polymorphic ventricular tachycardia: Success depends on substrate. Circ Arrhythm Electrophysiol. 2013;6(3):579–587. doi: https://doi.org/10.1161/CIRCEP.113.000170; Eckert H, El-Battrawy I, Veith M, et al. Pooled Analysis of Complications with Transvenous ICD Compared to Subcutaneous ICD in Patients with Catecholaminergic Polymorphic Ventricular Arrhythmia. J Pers Med. 2022;12(4):536. doi: https://doi.org/10.3390/jpm12040536.; Pizzale S, Gollob MH, Gow R, Birnie DH. Sudden death in a young man with catecholaminergic polymorphic ventricular tachycardia and paroxysmal atrial fibrillation. J Cardiovasc Electrophysiol. 2008;19(12):1319–1321. doi: https://doi.org/10.1111/j.1540-8167.2008.01211.x; Itoh H, Murayama T, Kurebayashi N, et al. Sudden death after inappropriate shocks of implantable cardioverter defibrillator in a catecholaminergic polymorphic ventricular tachycardia case with a novel RyR2 mutation. J Electrocardiol. 2021;69:111-118. doi: https://doi.org/10.1016/j.jelectrocard.2021.09.015; Richardson E, Spinks C, Davis A, et al. Psychosocial Implications of Living with Catecholaminergic Polymorphic Ventricular Tachycardia in Adulthood. J Genet Couns. 2018;27(3):549-557. doi: https://doi.org/10.1007/s10897-017-0152-1; Roses-Noguer F, Jarman JWE, Clague JR, Till J. Outcomes of defibrillator therapy in catecholaminergic polymorphic ventricular tachycardia. Heart Rhythm. 2014;11(1):58-66. doi: https://doi.org/10.1016/j.hrthm.2013.10.027; Roston TM, Jones K, Hawkins NM, et al. Implantable cardioverter-defibrillator use in catecholaminergic polymorphic ventricular tachycardia: A systematic review. Heart Rhythm. 2018;15(12):1791-1799. doi: https://doi.org/10.1016/j.hrthm.2018.06.046; Van Der Werf C, Lieve KV, Bos JM, et al. Implantable cardioverter-defibrillators in previously undiagnosed patients with catecholaminergic polymorphic ventricular tachycardia resuscitated from sudden cardiac arrest. Eur Heart J. 2019;40(35):2953-2961. doi: https://doi.org/10.1093/eurheartj/ehz309; Mohamed U, Gollob MH, Gow RM, Krahn AD. Sudden cardiac death despite an implantable cardioverter-defibrillator in a young female with catecholaminergic ventricular tachycardia. Heart Rhythm. 2006;3(12):1486-1489.; Sy RW, Gollob MH, Klein GJ, et al. Arrhythmia characterization and long-term outcomes in catecholaminergic polymorphic ventricular tachycardia. Heart Rhythm. 2011;8(6):864-871. doi: https://doi.org/10.1016/j.hrthm.2011.01.048; De Ferrari GM, Dusi V, Spazzolini C, et al. Clinical Management of Catecholaminergic Polymorphic Ventricular Tachycardia: The Role of Left Cardiac Sympathetic Denervation. Circulation. 2015;131(25):2185-2193. doi: https://doi.org/10.1161/CIRCULATIONAHA.115.015731; Schwartz PJ, Snebold NG, Brown AM. Effects of unilateral cardiac sympathetic denervation on the ventricular fibrillation threshold. Am J Cardiol. 1976;37(7):1034-1040. doi: https://doi.org/10.1016/0002-9149(76)90420-3; Yagishita D, Chui RW, Yamakawa K, et al. Sympathetic nerve stimulation, not circulating norepinephrine, modulates T-peak to T-end interval by increasing global dispersion of repolarization. Circ Arrhythm Electrophysiol. 2015;8(1):174-185. doi: https://doi.org/10.1161/CIRCEP.114.002195; Jonesco T. Traitement chirurgical de l'angine de poitrine par la resection dusympathique cervico-thoracique. Presse Med. 1921;20:30.; Moss AJ, McDonald J. Unilateral cervicothoracic sympathetic ganglionectomy for the treatment of long QT interval syndrome. N Engl J Med. 1971;285(16):903-904. doi: https://doi.org/10.1056/NEJM197110142851607; Schwartz PJ, Periti M, Malliani A. The long Q-T syndrome. Am Heart J. 1975;89(3):378-390. doi: https://doi.org/10.1016/0002-8703(75)90089-7; Schwartz PJ, Malliani A. Electrical alternation of the T-wave: clinical and experimental evidence of its relationship with the sympathetic nervous system and with the long Q-T syndrome. Am Heart J. 1975;89(1): 45-50. doi: https://doi.org/10.1016/0002-8703(75)90008-3; Wilde AAM, Bhuiyan ZA, Crotti L, et al. Left cardiac sympathetic denervation for catecholaminergic polymorphic ventricular tachycardia. N Engl J Med. 2008;358(19):2024-2029. doi: https://doi.org/10.1056/NEJMoa0708006; Atallah J, Fynn-Thompson F, Cecchin F, et al. Video-Assisted Thoracoscopic Cardiac Denervation: A Potential Novel Therapeutic Option for Children With Intractable Ventricular Arrhythmias. Ann Thorac Surg. 2008;86(5):1620-1625. doi: https://doi.org/10.1016/j.athoracsur.2008.07.006; Schwartz PJ, Ackerman MJ. Cardiac sympathetic denervation in the prevention of genetically mediated life-threatening ventricular arrhythmias. Eur Heart J. 2022;43(22):2096-2102. doi: https://doi.org/10.1093/eurheartj/ehac134; Cho Y. Left cardiac sympathetic denervation: An important treatment option for patients with hereditary ventricular arrhythmias. J Arrhythm. 2016;32(5):340-343. doi: https://doi.org/10.1016/j.joa.2015.08.002; Schwartz PJ, Locati EH, Moss AJ, et al. Left cardiac sympathetic denervation in the therapy of congenital long QT syndrome. A worldwide report. Circulation. 1991;84(2):503-511. doi: https://doi.org/10.1161/01.cir.84.2.503; Li C, Hu D, Shang L, et al. Surgical left cardiac sympathetic denervation for long QT syndrome: effects on QT interval and heart rate. Heart Vessels. 2005;20(4):137-141. doi: https://doi.org/10.1007/s00380-005-0820-1; Waddell-Smith KE, Ertresvaag KN, Li J, et al. Physical and Psychological Consequences of Left Cardiac Sympathetic Denervation in Long-QT Syndrome and Catecholaminergic Polymorphic Ventricular Tachycardia. Circ Arrhythm Electrophysiol. 2015;8(5): 1151-1158. doi: https://doi.org/10.1161/CIRCEP.115.003159; Dusi V, De Ferrari GM, Pugliese L, Schwartz PJ. Cardiac Sympathetic Denervation in Channelopathies. Front Cardiovasc Med. 2019;6:27. doi: https://doi.org/10.3389/fcvm.2019.00027; Perez PR, Hylind RJ, Roston TM, et al. Gene Therapy for Catecholaminergic Polymorphic Ventricular Tachycardia. Heart Lung Circ. 2023;32(7):790-797. doi: https://doi.org/10.1016/j.hlc.2023.01.018; https://vsp.spr-journal.ru/jour/article/view/3449

  2. 2
    Academic Journal

    المصدر: Rossiyskiy Vestnik Perinatologii i Pediatrii (Russian Bulletin of Perinatology and Pediatrics); Том 69, № 3 (2024); 6-18 ; Российский вестник перинатологии и педиатрии; Том 69, № 3 (2024); 6-18 ; 2500-2228 ; 1027-4065

    وصف الملف: application/pdf

    Relation: https://www.ped-perinatology.ru/jour/article/view/1997/1489; Elliott P.M., Anastasakis A., Borger M.A., Borggrefe M., Cecchi F., Charron P. еt 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): 2733–2779. DOI:10.1093/eurheartj/ehu284; Ommen S.R., Mital S., Burke M.A., Day S.M., Deswal A., Elliott 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: e159–e240. DOI:10.1016/j.jacc.020.08.045; Arbelo E., Protonotarios A., Gimeno J.R., Arbustini E., Barriales-Villa R., Basso C. et al. ESC Scientific Document Group2023 ESC Guidelines for the management of cardiomyopathies. Eur Heart J 2023; 44(37): 3503–3626. DOI:10.1093/eurheartj/ehad194; Maron B., Rowin E., Casey S., Lesser J., Garberich R., McGriff D.M. et al. Hypertrophic Cardiomyopathy in Children, Adolescents, and Young Adults Associated With Low Cardiovascular Mortality With Contemporary Management Strategies. Circulation 2016; 133(1): 62–73. DOI:10.1161/CIRCULATIONAHA.115.017633; Norrish G., Field E., Mcleod K., Ilina M., Stuart G., Bhole V. et al. Clinical presentation and survival of childhood hypertrophic cardiomyopathy: a retrospective study in United Kingdom. Eur Heart J 2019; 40: 986–993. DOI:10.1093/eurheartj/ehy798.; Marston N. A., Han L., Olivotto I., Day S. M., Ashley E. A., Michels M. et al. Clinical characteristics and outcomes in childhood-onset hypertrophic cardiomyopathy. Eur Heart J 2021; 42: 1988–1996. DOI:10.1093/eurheartj/ehab14; Kaski J. P., Kammeraad J. A. E., Blom N. A., Happonen J. M., Janousek J., Klaassen S. et al. Indications and management of implantable cardioverter-defibrillator therapy in childhood hypertrophic cardiomyopathy: A position statement from the AEPC Working Group on Basic Science, Genetics and Myocardial Disease and the AEPC Working Group on Cardiac Dysrhythmias and Electrophysiology. Cardiol Young 2023; 33(5): 681–698. DOI:10.1017/S1047951123000872; Norrish G., Cleary A., Field E., Cervi E., Boleti O., Ziółkowska L. et al. Clinical features and natural history of pread olescent non-syndromic hypertrophic cardiomyopathy. J Am CollCardiol 2022; 79: 1986–1997. DOI:10.1016/j.jacc.2022.03.347; Norrish G., Cantarutti N., Pissaridou E., Ridout D, Limongell G., Elliott P. et al. Risk factors for sudden cardiac death in childhood hypertrophic cardiomyopathy: A systematic review and meta-analysis. Eur J Prev Cardiol 2017; 24(11): 1220–1230. DOI:10.1177/2047487317702519; Ostman-Smith I., Wettrell G., Keeton B., Holmgren D, Ergander U., Gould S. et al. Age-and gender-specific mortality rates in childhood hypertrophic cardiomyopathy. Eur Heart J 2008; 29(9): 1160–1167. DOI:10.1093/eurheartj/ehn122; Miron A., Lafreniere-Roula M., Steve Fan C. P., Armstrong K. R., Dragulescu A., Papaz T. et al. A validated model for sudden cardiac death risk prediction in pediatric hypertrophic cardiomyopathy. Circulation 2020; 142: 217–229. DOI:10.1161/CIRCULATIONAHA.120.047235; Norrish G., Ding T., Field E., Ziólkowska L., Olivotto I., Limongelli G. et al. Development of a novel risk prediction model for sudden cardiac death in childhood hypertrophic cardiomyopathy (HCM risk-kids). JAMA Cardiol 2019; 4: 918–927. DOI:10.1001/jamacardio.2019.2861; Maurizi N., Passantino S., Spaziani G., Girolami F., Arretini A., Targetti M. et al. Long-term outcomes of pediatric-onset hypertrophic cardiomyopathy and age-specific risk factors forlethal arrhythmic events. JAMA Cardiol 2018; 3: 520–525. DOI:10.1001/jamacardio.2018.0789; Pettersen M.D., Du W., Skeens M.E., Humes, R.A. Regression equations for calculation of z scores of cardiac structures in a large cohort of healthy infants, children, and adolescents: an echocardiographic study. J Am Soc Echocardiogr 2008; 21(8): 922–934. DOI:10.1016/j.echo.2008.02.006; Lopez L., Frommelt P.C., Colan S.D., Trachtenberg F.L., Gongwer R., Stylianou M. et al. Pediatric Heart Network Echocardiographic Z Scores: Comparison with Other Published Models. J Am Soc Echocardiogr 2021; 34(2): 185–192. DOI:10.1016/j.echo.2020.09.019; Norrish G., Ding T., Field E., Cervi E., Ziółkowska L., Olivotto I. et al. Relationship Between Maximal Left Ventricular Wall Thickness and Sudden Cardiac Death in Childhood Onset Hypertrophic Cardiomyopathy. Circ Arrhythm Electrophysiol 2022; 15(5): e010075. DOI:10.1161/CIRCEP.121.010075; Ziolkowska L., Turska-Kmiec A., Petryka J., Kawalec W. Predictors of long-term outcome in children with hypertrophic cardiomyopathy. Pediatr Cardiol 2016; 37: 448–458. DOI:10.1007/s00246–015–1298-y; Balaji S., DiLorenzo M.P., Fish F.A., Etheridge S.P., Aziz P.F., Russell M.W. et al. Risk factors for lethal arrhythmicvents in children and adolescents with hypertrophic cardiomyopathy and an implantable defibrillator: an international multicenter study. Heart Rhythm 2019; 16: 1462–1467. DOI:10.1016/j.hrthm.2019.04.040; Ostman-Smith I., Sjoberg G., Rydberg A., Larsson P., Fernlund E. Predictors of risk for sudden death in childhood hypertrophic cardiomyopathy: the importance of the ECG risk score. Open Heart 2017; 4(2): e000658. Published 2017 Oct 21. DOI:10.1136/openhrt-2017–000658; Monserrat L., Elliott P.M., Gimeno J.R., Sharma S., PenasLado M., McKenna W.J. Non-sustained ventricular tachycardia in hypertrophic cardiomyopathy: an independent marker of sudden death risk in young patients. J Am Coll Cardiol 2003; 42(5): 873–879. DOI:10.1016/s0735-1097(03)00827-1; Norrish G., Chubb H., Field E., McLeod K., Ilina M., Spentzou G. et al. Clinical outcomes and programming strategies of implantable cardioverter-defibrillator devices in paediatric hypertrophic cardiomyopathy: a UK National Cohort Study. Europace 2021; 23(3): 400–408. DOI:10.1093/europace/euaa307; Fancia P., Santini D., Musumeci B., Semprini L., Adduci C., Pagannone E. et al. Clinical impact of nonsustained ventricular tachycardia recorded by the implantable cardioverter-defibrillator in patients with hypertrophic cardiomyopathy. J Cardiovasc Electrophysiol 2014; 25(11): 1180–1187. DOI:10.1111/jce.12492; Wang W., Lian Z., Rowin E.J., Maron B.J., Maron M.S., Link M.S. Prognostic Implications of Nonsustained Ventricular Tachycardia in High-Risk Patients With Hypertrophic Cardiomyopathy. Circ Arrhythm Electrophysiol 2017; 10(3): e004604. DOI:10.1161/CIRCEP.116.004604; Yang W.I., Shim C.Y., Kim Y.J., Kim S.A., Rhee S.J., Choi E.Y. et al. 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DOI:10.1016/j.ijcard.2022.09.044; Assaad I., Gauvreau K., Rizwan R., Margossian R., Colan S., Chen M.H. Value of Exercise Stress Echocardiography in Children with Hypertrophic Cardiomyopathy. J Am Soc Echocardiogr 2020; 33(7): 888–894.e2. DOI:10.1016/j.echo.2020.01.020; Xia K., Sun D., Wang R., Zhang Y. Factors associated with the risk of cardiac death in children with hypertrophic cardiomyopathy: a systematic review and meta-analysis. Heart Lung 2022; 52: 26–36. DOI:10.1016/j.hrtlng.2021.11.006; Östman-Smith I., Sjöberg G., Alenius Dahlqvist J., Larsson P., Fernlund E. Sudden cardiac death in childhood hypertrophic cardiomyopathy is best predicted by a combination of electrocardiogram risk-score and HCMRisk-Kids score. Acta Paediatr 2021; 110(11): 3105–3115. DOI:10.1111/apa.16045; Bonura E.D., Bos J.M., Abdelsalam M.A., Araoz P.A., Ommen S.R., Ackerman M.J. et al. 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    المصدر: The Siberian Journal of Clinical and Experimental Medicine; Том 38, № 4 (2023); 106-115 ; Сибирский журнал клинической и экспериментальной медицины; Том 38, № 4 (2023); 106-115 ; 2713-265X ; 2713-2927

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    المصدر: The Siberian Journal of Clinical and Experimental Medicine; Том 38, № 2 (2023); 235-240 ; Сибирский журнал клинической и экспериментальной медицины; Том 38, № 2 (2023); 235-240 ; 2713-265X ; 2713-2927

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    Academic Journal

    المصدر: Buletinul Academiei de Ştiinţe a Moldovei. Ştiinţe Medicale 72 (1) 82-90

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    Relation: info:eu-repo/grantAgreement/EC/FP7/17185/EU/Alternative terapeutice noi de ameliorere a prognozei de lungă durată a pacienților cu insuficiență cardiacă cronică prin implementarea strategiilor chirurgicale, intervenționale și de recuperare peri/20.80009.8007.34; https://ibn.idsi.md/vizualizare_articol/153777; urn:issn:18570011

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    المصدر: Translational Medicine; Том 9, № 1 (2022); 5-11 ; Трансляционная медицина; Том 9, № 1 (2022); 5-11 ; 2410-5155 ; 2311-4495

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  10. 10
    Academic Journal

    المساهمون: The study was performed with the support of the National Medical Research Centre of Cardiology named after academician E.I. Chazov., Исследование проведено при поддержке Национального медицинского исследовательского центра кардиологии.

    المصدر: Rational Pharmacotherapy in Cardiology; Vol 18, No 4 (2022); 427-432 ; Рациональная Фармакотерапия в Кардиологии; Vol 18, No 4 (2022); 427-432 ; 2225-3653 ; 1819-6446

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    المصدر: FARMAKOEKONOMIKA. Modern Pharmacoeconomics and Pharmacoepidemiology; Vol 15, No 1 (2022); 5-22 ; ФАРМАКОЭКОНОМИКА. Современная фармакоэкономика и фармакоэпидемиология; Vol 15, No 1 (2022); 5-22 ; 2070-4933 ; 2070-4909

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    المصدر: Current Pediatrics; Том 18, № 2 (2019); 125-133 ; Вопросы современной педиатрии; Том 18, № 2 (2019); 125-133 ; 1682-5535 ; 1682-5527

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    المصدر: Siberian Journal of Clinical and Experimental Medicine; Том 34, № 1 (2019); 39-47 ; Сибирский журнал клинической и экспериментальной медицины; Том 34, № 1 (2019); 39-47 ; 2713-265X ; 2713-2927 ; 10.29001/2073-8552-2019-34-1

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    المصدر: Rational Pharmacotherapy in Cardiology; Vol 14, No 4 (2018); 605-611 ; Рациональная Фармакотерапия в Кардиологии; Vol 14, No 4 (2018); 605-611 ; 2225-3653 ; 1819-6446 ; 10.20996/1819-6446-2018-14-4

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    المصدر: General Reanimatology; Том 14, № 1 (2018); 58-67 ; Общая реаниматология; Том 14, № 1 (2018); 58-67 ; 2411-7110 ; 1813-9779 ; 10.15360/1813-9779-2018-1

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