Диссертация (1139848), страница 44
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Heart. J. – 2018. – Vol. 39(21). – P. 1883–1948. – URL: https://academic.oup.com/eurheartj/article/39/21/1883/4939241.38. Buja, G. Right ventricula cardiomyopathy in identical and nonidentical young twins /G. Buja, A. Nava, L. Daliento, R. Scognamiglio et al. // Am Heart J. – 1993. – Vol. 126(5), Nov. –P. 1187–1193.39. Burke, A.P. Arrhythmogenic right ventricular cardiomyopathy and fatty replacement of theright ventricular myocardium: are they different diseases? / A.P. Burke, A.
Farb, G. Tashko,R. Virmani // Circulation. – 1998. – Vol. 97(16). – P. 1571–1580.40. Calabrese, F. Arrhythmogenic right ventricular cardiomyopathy/ dysplasia: is there arole for viruses? / F. Calabrese, C. Basso, E. Carturan et al. // Cardiovascular Pathology. – 2006. –Vol. 15(1). – P. 11–17.41. Calkins, H. Arrhythmogenic right ventricular dysplasia / H.
Calkins // Curr. Probl.Cardiol. – 2013. – Vol. 38(3). – P. 103–123.42. Calkins, H. Arrhythmogenic Right Ventricular Dysplasia/Cardiomyopathy – ThreeDecades of Progress / H. Calkins // Circulation Journal. – 2015. – Vol. 79(5). – P. 902–913.43. Calkins, H. Risk Stratification in Arrhythmogenic Right Ventricular Cardiomyopathy /H. Calkins, D. Corrado, F. Marcus // Circulation. – 2017. – Vol. 136(21). – P.
2068–2082. – URL:https://www.ahajournals.org/doi/10.1161/CIRCULATIONAHA.117.030792.44. Campian, M.E. Assessment of inflammation in patients with arrhythmogenic rightventricular cardiomyopathy/dysplasia / M.E. Campian, H.J. Verberne, M. Hardziyenka, E. de Groot etal. // Eur. J. Nucl.
Med. Mol. Imaging. – 2010. – Vol. 37. – P. 2079–2085.45. Campian, M.E. Early inflammatory response during development of right ventricular heartfailure in a rat model / M.E. Campian, M. Hardziyenka, K. de Bruin, B.L.F. van Eck-Smit et al. // Eur. J.Heart Fail. – 2010. – Vol. 12. – P. 653–658.20846. Campuzano, O. Arrhythmogenic right ventricular cardiomyopathy: severe structuralalterations are associated with inflammation / O. Campuzano, M. Alcalde, A.
Iglesias, C. BarahonaDussault et al. // J. Clin. Pathol. – 2012. – Vol. 65(12). – P. 1077–1083.47. Campuzano, O. Genetics of arrhythmogenic right ventricular cardiomyopathy /O. Campuzano, M. Alcalde, C. Allegue et al. // J. Med. Genet. – 2013. – Vol. 50. – P. 280–289.48. Carlson, M.D. Right ventricular outflow tract ventricular tachycardia: detection ofpreviously unrecognized anatomic abnormalities using cine magnetic resonance imaging /M.D.
Carlson, R.D. White, R.G. Trohman, L.P. Adler et al. // J. Am. Coll. Cardiol. – 1994. –Vol. 24(3). – P. 720–727.49. Chelko, S.P. Central role for GSK3β in the pathogenesis of arrhythmogeniccardiomyopathy / S.P. Chelko, A. Asimaki, P. Andersen, D. Bedja et al. // JCI Insight. – 2016. –Vol. 1(5). – URL: https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4861310.50.
Chimenti, C. Histologic Findings in Patients With Clinical and Instrumental Diagnosis ofSporadic Arrhythmogenic Right Ventricular Dysplasia / C. Chimenti, M. Pieroni, A. Maseri et al. //Journal of the American College of Cardiology. – 2004. – Vol. 43(12). – P. 2306–2313.51. Chin, T.K. Isolated noncompaction of left ventricular myocardium: a study of eight cases /T.K. Chin, J.K. Perloff, R.G.
Williams et al. // Circulation. – 1990. – Vol. 82(2). – P. 507–513.52. Christensen, A.H.MyocarditisMimickingArrhythmogenicRightVentricularCardiomyopathy / A.H. Christensen, J.H. Svendsen // JACC. – 2009. – Vol. 54(7). – P. 663–664.53. Coonar, A.S. Gene for arrhythmogenic right ventricular cardiomyopathy with diffusenonepidermolytic palmoplantar keratoderma and woolly hair (Naxos disease) maps to 17q21 /A.S. Coonar, N. Protonotarios, A. Tsatsopoulou, E.W. Needham et al. // Circulation. – 1998. –Vol. 97(20). – P. 2049–2058.54.
Corcioli, F. Tissue persistence of parvovirus B19 genotypes in asymptomatic persons /F. Corcioli, K. Zakrzewska, A. Rinieri et al. // J. Med. Virol. – 2008. – Vol. 80(11). – P. 2005–2011.55. Corrado, D. Arrhythmogenic right ventricular cardiomyopathy and sports activity /D. Corrado, A. Zorzi // Eur. Heart J. – 2015.
– Vol. 36(27). – P. 1708–1710.56. Corrado, D. Arrhythmogenic right ventricular cardiomyopathy: diagnosis, prognosis,and treatment / D. Corrado, C. Basso, G. Thiene // Heart. – 2000. – Vol. 83(5). – P. 588–595.57. Corrado, D. Does sports activity enhance the risk of sudden death in adolescents and youngadults? / D. Corrado, C. Basso, G. Rizzoli, M. Schiavon, G.
Thiene // J. Am. Coll. Cardiol. – 2003. –Vol. 42(11). – P. 1959–1963.58. Corrado, D. Familial cardiomyopathy underlies syndrome of right bundle branch block, STsegment elevation and sudden death / D. Corrado, A. Nava, G. Buja, B. Martini et al. // J. Am. Coll.Cardiol. – 1996. – Vol. 27(2). – P. 443–448.20959. Corrado, D.
Implantable cardioverter-defibrillator therapy for prevention of sudden death inpatients with arrhythmogenic right ventricular cardiomyopathy/dysplasia / D. Corrado, L. Leoni,M.S. Link, B.P. Della et al. // Circulation. – 2003. – Vol. 108(25).
– P. 3084–3091.60. Corrado, D. Molecular biology and clinical management of arrhythmogenic rightventricular cardiomyopathy/dysplasia / D. Corrado, C. Basso, K. Pilichou, G. Thiene. – Heart. –2011. – Vol. 97(7). – P. 530–539.61. Corrado, D. Prophylactic implantable defibrillator in patients with arrhythmogenic rightventricular cardiomyopathy/dysplasia and no prior ventricular fibrillation or sustained ventriculartachycardia / D. Corrado, H.
Calkins, M.S. Link, L. Leoni et al. // Circulation. – 2010. – Vol. 122(12). –P. 1144–1152.62. Corrado, D. Screening for hypertrophic cardiomyopathy in young athletes / D. Corrado,C. Basso, M. Schiavon, G. Thiene // N. Engl. J. Med. – 1998. – Vol. 339(6). – P. 364–369.63. Corrado, D. Spectrum of clinicopathologic manifestation of arrhythmogenic rightventricular cardiomyopathy/dysplasia: a multicenter study / D. Corrado, C. Basso, G.
Thiene,W.J. McKenna et al. // J. Am. Coll. Cardiol. – 1997. – Vol. 30(6). – P. 1512–1520.64. Corrado, D. Sudden death in young competitive athletes: clinicopathologic correlations in22 cases / D. Corrado, G. Thiene, A. Nava, L. Rossi, N. Pennelli // Am. J. Med. – 1990.
– Vol. 89(5). –P. 588–596.65. Corrado, D. Sudden death in young people with apparently isolated mitral valve prolapsed /D. Corrado, C. Basso, A. Angelini, G. Thiene // Pacing Clin Electrophysiol. – 1997. – Vol. 27(11). –P. 1097–1105.66. Corrado, D. Thiene does implantable cardioverter-defibrillator therapy modify thenatural history of arrhythmogenic right ventricular cardiomyopathy / D. Corrado, L. Leoni, G. Buja //Italian Heart J.
– 2004. – Vol. 5, Suppl. 1. – P. 72–75.67. Corrado, D. Three-dimensional electroanatomical voltage mapping and histologicevaluation of myocardial substrate in right ventricular outflow tract tachycardia / D. Corrado, C. Basso,L. Leoni, B. Tokajuk et al. // J. Am. Coll. Cardiol. – 2008. – Vol. 51(7). – P. 731–739.68. Corrado, D. Treatment of arrhythmogenic right ventricular cardiomyopathy/ dysplasia:an international task force consensus statement / D. Corrado, T.
Wichter, M.S. Link, R.N. Hauer etal. // Eur. Heart J. – 2015. – Vol. 36. – P. 3227–3237.69. Corrado, D. Trends in sudden cardiovascular death in young competitive athletes afterimplementation of a preparticipation screening program / D. Corrado, C. Basso, A. Pavei,P. Michieli et al. // JAMA. – 2006. – Vol. 296(13). – P.
1593–1601.70. Cox, M.G. Arrhythmogenic Right Ventricular Dysplasia/Cardiomyopathy Diagnostic TaskForce Criteria. Impact of New Task Force Criteria / M.G. Cox, J.J. van der Smagt, M. Noorman et al. //Circulation: Arrhythmia and Electrophysiology. – 2010. – Vol. 3(2). – P. 126–133.21071. Dalal, D. Arrhythmogenic Right Ventricular Dysplasia: a United States Experience /D.
Dalal, K. Nasir, Ch. Bomma, K. Prakasa et al. // Circulation. – 2005. – Vol. 112(25). – P. 3823–3832.72. Dalal, D. Long-term efficacy of catheter ablation of ventricular tachycardia in patientswith arrhythmogenic right ventricular dysplasia/cardiomyopathy / D. Dalal, R. Jain, H. Tandri etal. // J. Am. Coll. Cardiol. – 2007. – Vol. 50(5). – P. 432–440.73. De la Grandmaison, G.L. Is there progress in the autopsy diagnosis of suddenunexpected death in adults? / G.L. de la Grandmaison // Forensic Science International. – 2006. –Vol. 156 (2-3). – P. 138–144.74. De Noronha, S.V. Aetiology of sudden cardiac death in athletes in the United Kingdom:a pathological study / S.V.
de Noronha, S. Sharma, M. Papadakis, S. Desai et al. // Heart. – 2009. –Vol. 95(17). – P. 1409–1414.75. Douglas, P.S. Different effects of prolonged exercise on the right and left ventricles /P.S. Douglas, M.L. O’Toole, W.D.B. Hiller, N. Reichek // J. Am. Coll. Cardiol. – 1990. –Vol. 15(1). – P. 64–69.76. Elliott, P. Classification of the cardiomyopathies: a position statement from the Europeansociety of cardiology working group on myocardial and pericardial diseases / P.
Elliott, B. Andersson,E. Arbustini et al. // Eur. Heart J. – 2008. – Vol. 29(2). – P. 270–276.77. Elmaghawry, M. A global perspective of arrhythmogenic right ventricular cardiomyopathy / M. Elmaghawry, M. Alhashemi, A. Zorzi, M.H. Yacoub // Global Cardiology Scienceand Practice. – 2013. – Vol. 2012(2). – P. 81–91.78.
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