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Quoted phrase not found in phrase index: "Arrhythmogenic right ventricular dysplasia 9"
Page 1
Diagnostic and therapeutic strategies for arrhythmogenic right ventricular dysplasia/cardiomyopathy patient.
Wang W, James CA, Calkins H. Wang W, et al. Europace. 2019 Jan 1;21(1):9-21. doi: 10.1093/europace/euy063. Europace. 2019. PMID: 29688316 Free PMC article. Review.
Arrhythmogenic right ventricular dysplasia/cardiomyopathy (ARVD/C) is a rare inherited heart muscle disease characterized by ventricular tachyarrhythmia, predominant right ventricular dysfunction, and sudden cardiac death. ...Exerc
Arrhythmogenic right ventricular dysplasia/cardiomyopathy (ARVD/C) is a rare inherited heart muscle disease char
Myocardial voltage ratio in arrhythmogenic right ventricular dysplasia/cardiomyopathy.
Müssigbrodt A, Bertagnolli L, Efimova E, Kosiuk J, Dinov B, Bode K, Kircher S, Dagres N, Döring M, Richter S, Sommer P, Husser D, Bollmann A, Hindricks G, Arya A. Müssigbrodt A, et al. Herzschrittmacherther Elektrophysiol. 2017 Jun;28(2):219-224. doi: 10.1007/s00399-017-0508-0. Epub 2017 May 23. Herzschrittmacherther Elektrophysiol. 2017. PMID: 28536891 Review. English.
AIMS: This study aimed to analyze the influence of scar distribution between the endocardium and the epicardium in patients with arrhythmogenic right ventricular dysplasia/cardiomyopathy (ARVD/C). METHODS: Electroanatomical mapping data were derived fr …
AIMS: This study aimed to analyze the influence of scar distribution between the endocardium and the epicardium in patients with arrhythm
A new prediction model for ventricular arrhythmias in arrhythmogenic right ventricular cardiomyopathy.
Cadrin-Tourigny J, Bosman LP, Nozza A, Wang W, Tadros R, Bhonsale A, Bourfiss M, Fortier A, Lie ØH, Saguner AM, Svensson A, Andorin A, Tichnell C, Murray B, Zeppenfeld K, van den Berg MP, Asselbergs FW, Wilde AAM, Krahn AD, Talajic M, Rivard L, Chelko S, Zimmerman SL, Kamel IR, Crosson JE, Judge DP, Yap SC, van der Heijden JF, Tandri H, Jongbloed JDH, Guertin MC, van Tintelen JP, Platonov PG, Duru F, Haugaa KH, Khairy P, Hauer RNW, Calkins H, Te Riele ASJM, James CA. Cadrin-Tourigny J, et al. Eur Heart J. 2022 Aug 21;43(32):e1-e9. doi: 10.1093/eurheartj/ehac180. Eur Heart J. 2022. PMID: 35441664 Free PMC article.
AIMS: Arrhythmogenic right ventricular dysplasia/cardiomyopathy (ARVC) is characterized by ventricular arrhythmias (VAs) and sudden cardiac death (SCD). ...Eight potential predictors were pre-specified: age, sex, cardiac syncope in the pr …
AIMS: Arrhythmogenic right ventricular dysplasia/cardiomyopathy (ARVC) is characterized by ventricular ar …
Bradyarrhythmias in Arrhythmogenic Right Ventricular Cardiomyopathy.
Liang E, Wu L, Fan S, Li X, Hu F, Zheng L, Fan X, Chen G, Ding L, Yao Y. Liang E, et al. Am J Cardiol. 2019 May 15;123(10):1690-1695. doi: 10.1016/j.amjcard.2019.02.032. Epub 2019 Feb 23. Am J Cardiol. 2019. PMID: 30885416
Less is known about bradyarrhythmias in arrhythmogenic right ventricular cardiomyopathy (ARVC). This cross-sectional study aimed to assess the prevalence and clinical significance of bradyarrhythmias in ARVC. ...A total of 169 patients (32.4%) presented with …
Less is known about bradyarrhythmias in arrhythmogenic right ventricular cardiomyopathy (ARVC). This cross-sectional st …
Analysis of ventricular function by CT.
Rizvi A, Deaño RC, Bachman DP, Xiong G, Min JK, Truong QA. Rizvi A, et al. J Cardiovasc Comput Tomogr. 2015 Jan-Feb;9(1):1-12. doi: 10.1016/j.jcct.2014.11.007. Epub 2014 Nov 26. J Cardiovasc Comput Tomogr. 2015. PMID: 25576407 Free PMC article. Review.
The assessment of ventricular function, cardiac chamber dimensions, and ventricular mass is fundamental for clinical diagnosis, risk assessment, therapeutic decisions, and prognosis in patients with cardiac disease. Although cardiac CT is a noninvasive imagin …
The assessment of ventricular function, cardiac chamber dimensions, and ventricular mass is fundamental for clinical diagnosis …
Arrhythmogenic Cardiomyopathy and Athletes: A Dangerous Relationship.
de la Guía-Galipienso F, Ugedo-Alzaga K, Grazioli G, Quesada-Ocete FJ, Feliu-Rey E, Perez MV, Quesada-Dorador A, Sanchis-Gomar F. de la Guía-Galipienso F, et al. Curr Probl Cardiol. 2023 Sep;48(9):101799. doi: 10.1016/j.cpcardiol.2023.101799. Epub 2023 May 11. Curr Probl Cardiol. 2023. PMID: 37172878 Review.
Arrhythmogenic cardiomyopathy (ACM) is a disease characterized by a progressive replacement of myocardium by fibro-adipose material, predisposing to ventricular arrhythmias (VA) and sudden cardiac death (SCD). ...Here, we review the potential implications of exercis
Arrhythmogenic cardiomyopathy (ACM) is a disease characterized by a progressive replacement of myocardium by fibro-adipose material,
Arrhythmogenic right ventricular cardiomyopathy/dysplasia: risk stratification and therapy.
Buja G, Estes NA 3rd, Wichter T, Corrado D, Marcus F, Thiene G. Buja G, et al. Prog Cardiovasc Dis. 2008 Jan-Feb;50(4):282-93. doi: 10.1016/j.pcad.2007.10.004. Prog Cardiovasc Dis. 2008. PMID: 18156007 Free PMC article. Review.
Arrhythmogenic right ventricular cardiomyopathy/dysplasia (ARVC/D) is an inherited heart muscle disease that occurs primarily in young and middle-age individuals. ...The main questions regarding the risk stratification and the therapeutic strategy in A
Arrhythmogenic right ventricular cardiomyopathy/dysplasia (ARVC/D) is an inherited heart muscle disease that occ
Pregnancy and newborn outcomes in arrhythmogenic right ventricular cardiomyopathy/dysplasia.
Gandjbakhch E, Varlet E, Duthoit G, Fressart V, Charron P, Himbert C, Maupain C, Bordet C, Hidden-Lucet F, Nizard J. Gandjbakhch E, et al. Int J Cardiol. 2018 May 1;258:172-178. doi: 10.1016/j.ijcard.2017.11.067. Int J Cardiol. 2018. PMID: 29544927
INTRODUCTION: The prognosis of pregnancy in patients with Arrhythmogenic Right Ventricular Cardiomyopathy/dysplasia (ARVC/D) is poorly documented. ...CONCLUSION: ARVC/D is associated with a low rate of major cardiac events during pregnancy and v …
INTRODUCTION: The prognosis of pregnancy in patients with Arrhythmogenic Right Ventricular Cardiomyopathy/dys
Pathophysiology of arrhythmogenic cardiomyopathy.
Basso C, Bauce B, Corrado D, Thiene G. Basso C, et al. Nat Rev Cardiol. 2011 Nov 29;9(4):223-33. doi: 10.1038/nrcardio.2011.173. Nat Rev Cardiol. 2011. PMID: 22124316 Review.
Arrhythmogenic cardiomyopathy (AC) is a clinically and genetically heterogeneous disorder of heart muscle that is associated with ventricular arrhythmias and risk of sudden cardiac death, particularly in the young and athletes. ...
Arrhythmogenic cardiomyopathy (AC) is a clinically and genetically heterogeneous disorder of heart muscle that is associated with
Utility of Left and Right Ventricular Strain in Arrhythmogenic Right Ventricular Cardiomyopathy: A Prospective Multicenter Registry.
Namasivayam M, Bertrand PB, Bernard S, Churchill TW, Khurshid S, Marcus FI, Mestroni L, Saffitz JE, Towbin JA, Zareba W, Picard MH, Sanborn DY; North American ARVC Registry. Namasivayam M, et al. Circ Cardiovasc Imaging. 2023 Dec;16(12):e015671. doi: 10.1161/CIRCIMAGING.123.015671. Epub 2023 Dec 19. Circ Cardiovasc Imaging. 2023. PMID: 38113321
BACKGROUND: Imaging evaluation of arrhythmogenic right ventricular cardiomyopathy (ARVC) remains challenging. Myocardial strain assessment by echocardiography is an increasingly utilized technique for detecting subclinical left ventricular (LV) and …
BACKGROUND: Imaging evaluation of arrhythmogenic right ventricular cardiomyopathy (ARVC) remains challenging. Myocardia …
239 results