Диссертация (1139848), страница 45
Текст из файла (страница 45)
Finsterer, J. Role of desmoplakin mutations in the pathogenesis of non-compaction /J. Finsterer, C. Stöllberger // EP Europace. – 2015. – Vol. 7(2). – P. 334. – URL:https://academic.oup.com/europace/article/17/2/334/2802580.79. Fontaine, G. Arrhythmogenic Right Ventricular Cardiomyopathies: Clinical Forms andMain Differential Diagnoses / G. Fontaine, F.
Fontaliran, R. Frank // Circulation. – 1998. –Vol. 97. – P. 1532–1535.80. Fontaine, G. Arrhythmogenic right ventricular dysplasia / G. Fontaine, F. Fontaliran,J.L. Herbert et al. // Ann. Rev. Med. – 1999. – Vol. 50. – P. 17–35.81. Fontaine, G. Arrhythmogenic right ventricular dysplasia back in force / G.
Fontaine,H.S. Chen // Am. J. Cardiol. – 2014. – Vol. 113(10). – P. 1735–1739.82. Fontaine, G. Outcome of arrhythmogenic right ventricular dysplasia. Apropos of 4case / G. Fontaine, C. Brestescher, F. Fontaliran et al. // Arch. Mal. Coeur. Vaiss. – 1995.
–Vol. 88(7). – P. 973–979.21183. Fontaine, G. Stimulation studies and epicardial mapping in VT: Study of mechanismsand selection for surgery / G. Fontaine, G. Guiraudon, R. Frank et al. // Reentrant Arrhythmias / Ed.by H. E. Kulbertus.
– Lancaster, PA: MTP Publishers, 1977. – P. 334–350.84. Fontaine, G. Sus-decalage du segment ST en derivations precordiales droites et mort subite:relation avec la dysplasie ventriculaire droite arythmogene / G. Fontaine, O. Piot, P.S. Sohal, Y. Issi etal. // Arch. Mai.
Coeur. – 1996. – Vol. 89. – P. 1323–1329.85. Fontaine, G. The arrhythmogenic right ventricle: dysplasia versus cardiomyopathy /G. Fontaine, F. Fontaliran, F.R. Andrade, E. Velazquez et al. // Heart Vessels. – 1995. – Vol. 10(5). –P. 227–235.86. Fontaine, G. The multiple facets of right ventricular cardiomyopathies / G. Fontaine //European Heart Journal. – 2011. – Vol. 32, Issue 9, 1 May 2011, Pages 1049–1051,https://doi.org/10.1093/eurheartj/ehr08887. Fontaine, G. Ventricular tachycardia catheter ablation in arrhythmogenic rightventricular dysplasia: a 16-year experience / G. Fontaine, J. Tonet, Y. Gallais, et al.
// Curr. Cardiol.Rep. – 2000. – Vol. 2(6). – P. 498–506.88. Fontaliran, F. Signification del infiltrats lymphoplasmocytaires dans la dyplasiaventriculare droite arhythmogene / F. Fontaliran, G. Fontaine, C. Brestescher, J. Labrousee, F. Vilde// Arch. Mal. Coeur. – 1995. – Vol. 88(7). – P. 1021–1028.89. Fox, P.R. Spontaneously occurring arrhythmogenic right ventricular cardiomyopathy in thedomestic cat: A new animal model similar to the human disease / P.R.
Fox, B.J. Maron, C. Basso,S.K. Liu, G. Thiene // Circulation. – 2000. – Vol. 102(15). – P. 1863–1870.90. Fressart, V.Desmosomalgeneanalysisinarrhythmogenicrightventriculardysplasia/cardiomyopathy:spectrum of mutations and clinical impact in practice / V. Fressart,G. Duthoit, E. Donal, V. Probst et al. // Europace. – 2010. – Vol. 12(6). – P. 861–868.91. Fye, W.B. Giovanni Maria Lancisi, 1654–1720 / W.B.
Fye // Clinical Cardiology. –1990. – Vol. 13(9). – P. 670–671.92. Gallo, P. Pathologic evidence of extensive left ventricular involvement in arrhythmogenicright ventricular cardiomyopathy / P. Gallo, G. D'Amati, F. Pelliccia // Hum. Pathol. – 1992. –Vol. 23(8). – P. 948–952.93. Garcia, F.C. Epicardial substrate and outcome with epicardial ablation of ventriculartachycardia in arrhythmogenic right ventricular cardiomyopathy/dysplasia / F.C. Garcia, V. Bazan,E.S. Zado, J.F. Ren, F.E. Marchlinski // Circulation. – 2009.
– Vol. 120(5). – P. 366–375.94. Garcia-Gras, E. Suppression of canonical Wnt/beta-catenin signaling by nuclearplakoglobin recapitulates phenotype of arrhythmogenic right ventricular cardiomyopathy /E. Garcia-Gras, R. Lombardi, M.J. Giocondo, J.T. Willerson et al. // J. Clin. Invest. – 2006.
–Vol. 116(7). – P. 2012–2021.21295.Gemayel, C. ArrhythmogenicRightVentricularCardiomyopathy/C. Gemayel,A. Pelliccia, P.D. Thompson // J. Am. Coll. Cardiol. – 2001. – Vol. 38(7). – P. 1773–1781.96.Gerlis, L.M. Dysplastic conditions of the right ventricular myocardium: Uhl's's anomalyversus arrhythmogenic right ventricular dysplasia / L.M. Gerlis, S.C. Schmidt-Ott, S.Y. Ho,R.H. Anderson // Br.
Heart J. –1993. Vol. 69(2). – P. 142–150.97.Gilotra, N.A. Heart Failure Is Common and Under-Recognized in Patients WithArrhythmogenic Right Ventricular Cardiomyopathy/Dysplasia / N.A. Gilotra, A. Bhonsale,C.A. James, A.S.J. te Riele et al. // Circ Heart Fail. – 2017. – Vol. 10(9). – URL:https://www.ahajournals.org/doi/10.1161/CIRCHEARTFAILURE.116.003819.98.Girard, F.
Catastrophic global heart failure in a case of non arrhythmogenic rightventricular dysplasia / F. Girard, G. Fontaine, F. Fontaliran, O. Zenati, P. Gajdos // Heart Vessels. –1997. – Vol. 12(3). – P. 152–154.99.Groeneweg, J.A. Clinical Presentation, Long-Term Follow-Up, and Outcomes of 1001Arrhythmogenic Right Ventricular Dysplasia/Cardiomyopathy Patients and Family Members / J.A.Groeneweg, A. Bhonsale, C.A.
James, A.S. te Riele et al. // Circ Cardiovasc Genet. – 2015. –Vol. 8(3), Jun. – P. 437–446.100. Hariharan, V. Arrhythmogenic right ventricular cardiomyopathy mutations alter shearresponse without changes in cell–cell adhesion / V. Hariharan, A. Asimaki, J.E. Michaelson, E. Plovieet al. // Cardiovascular Research. – 2014. – Vol. 104(4). – P. 280–289.101. Hashimura, H.Radiologic-PathologicCorrelationofPrimaryandSecondaryCardiomyopathies: MR Imaging and Histopathologic Findings in Hearts from Autopsy andTransplantation / H.
Hashimura, F. Kimura, H. Ishibashi-Ueda, Y. Morita et al. // RadioGraphics. –2017. – Vol. 37(3). – URL: https://pubs.rsna.org/doi/full/10.1148/rg.2017160082.102. Heart Failure Is Common and Under-Recognized in Patients With ArrhythmogenicRight Ventricular Cardiomyopathy/Dysplasia / N.A. Gilotra, A.
Bhonsale, C.A. James, A.S.J. teRiele et al. // Circ. Heart Fail. – 2017. – Vol. 10(9). – URL: https://www.ahajournals.org/doi/10.1161/CIRCHEARTFAILURE.116.003819.103. Heim, A. Enterovirus heart disease of adults: a persistent, limited organ infection inthe presence of neutralizing antibodies / A. Heim, I.
Grumbach, S. Hake, G. Muller et al. // J. Med.Virol. – 1997. – Vol. 53(3). – P. 196– 204.104. Henningsen, K.M.A. Prognostic impact of hs-CRP and IL-6 in patients with persistentatrial fibrillation treated with electrical cardioversion / K.M.A. Henningsen, S.K. Therkelsen,H. Bruunsgaard, K.S. Krabbe et al. // Scandinavian Journal of Clinical and LaboratoryInvestigation. – 2009. – Vol.
69(3). – P. 425–432.105. Herren, T. Arrhythmogenic right ventricular cardiomyopathy/dysplasia: a not so rare‘disease of the desmosome’ with multiple clinical presentations / T. Herren, P.A. Gerber, F. Duru //Clin. Res. Cardiol. – 2009. – Vol. 98(3). – P. 141–158.213106. Hershberger, R.E. Dilated cardiomyopathy: the complexity of a diverse geneticarchitecture / R.E.
Hershberger , D.J. Hedges, A. Morales // Nat. Rev. Cardiol. – 2013. – Vol. 10(9). –P. 531–547. – URL: https://www.nature.com/articles/nrcardio.2013.105.107. Hoffmayer, K.S. Electrocardiographic comparison of ventricular arrhythmias in patientswith arrhythmogenic right ventricular cardiomyopathy and right ventricular outflow tract tachycardia /K.S.
Hoffmayer, O.N. Machado, G.M. Marcus et al. // JACC. – 2011. – Vol. 58(8). – P. 831–838.108. Hulot, J.S. Natural history and risk stratification of arrhythmogenic right ventriculardysplasia/cardiomyopathy / J.S. Hulot, X. Jouven, J.P. Empana, R.
Frank, G. Fontaine //Circulation. – 2004. – Vol. 110(14). – P. 1879 –1884.109. Ilyas, S. Sudden death and isolated right ventricular noncompaction cardiomyopathy:report of 2 autopsied adult cases / S. Ilyas, C. Ganote, D. Lajoie, J. Robertson, K. ClineParhamovich // Am. J. Forensic. Med. Pathol. – 2013. – Vol. 34(3). – P. 225–227.110. Indik, J.H.
Do patients with right ventricular outflow tract ventricular arrhythmias have anormal right ventricula rwall motion? A quantitative analysis compared to normal subjects / J.H. Indik,W.J. Dallas, T. Ovitt, T. Wichter et al. // Cardiology. – 2005. – Vol. 104. – P. 10–15.111. James, C.A. Exercise increases age-related penetrance and arrhythmic risk inarrhythmogenic right ventricular dysplasia/cardiomyopathy-associated desmosomal mutationcarriers / C.A.
James, A. Bhonsale, C. Tichnell, B. Murray et al. // J. Am. Coll. Cardiol. – 2013. –Vol. 62(14). – P. 1290–1297.112. James, T.N. Apoptosis and the heart / T.N. James // Arrhythmogenic right ventricularcardiomyopathy / dysplasia / Ed. by: A. Nava, L Rossi, G Thiene. – Amsterdam: Elsevier, 1997. –P. 113–138.113. Jenni, R. Isolated ventricular noncompaction of the myocardium in adults / R. Jenni,E.
Oechslin, B. van der Loo // Heart. – 2007. – Vol. 93(1). – P. 11–15. – URL:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1861330.114. Kimura, Y. Heart failure in patients with arrhythmogenic right ventricularcardiomyopathy: What are the risk factors? / Y. Kimura, T. Noda, T.A. Matsuyama, Y. Otsuka etal. // Int. J. Cardiol. – 2017. – Vol. 241. – P. 288–294.115. Kostis, W.J. Troponin-I elevation in a young man with arrhythmogenic right ventriculardysplasia/cardiomyopathy / W.J.
Kostis, R.J. Tedford, D.L. Miller, S.P. Schulman, G.F. Tomaselli /J. Interv. Card. Electrophysiol. – 2008. – Vol. 22(1). – P. 49–53.116. Lancisi, G.M. De subitaneis mortibus / G.M. Lancisi. – Rome: Friderici Gleditsch,1709. – 371 p.117. Lancisi, G.M. De motu cordis et aneurysmatibus, opus posthumum in duas partesdivisum / G.M.
![](https://s.studizba.com/z.php?f=/templates/si/i/noavatar.png&w=100&h=100&t=1"){kind=avatar}
