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1989
2025

Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1989 1
1990 1
1992 1
1993 2
1994 1
1995 3
1996 2
1997 4
1998 3
2000 6
2001 6
2002 4
2003 4
2004 7
2005 9
2006 6
2007 4
2008 11
2009 9
2010 4
2011 3
2012 7
2013 4
2014 13
2015 6
2016 10
2017 14
2018 10
2019 11
2020 2
2021 6
2022 7
2023 7
2024 4
2025 1

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172 results

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Page 1
Arrhythmogenic Right Ventricular Cardiomyopathy.
Corrado D, Link MS, Calkins H. Corrado D, et al. N Engl J Med. 2017 Jan 5;376(1):61-72. doi: 10.1056/NEJMra1509267. N Engl J Med. 2017. PMID: 28052233 Review. No abstract available.
Arrhythmogenic Right Ventricular Cardiomyopathy.
Krahn AD, Wilde AAM, Calkins H, La Gerche A, Cadrin-Tourigny J, Roberts JD, Han HC. Krahn AD, et al. JACC Clin Electrophysiol. 2022 Apr;8(4):533-553. doi: 10.1016/j.jacep.2021.12.002. JACC Clin Electrophysiol. 2022. PMID: 35450611 Free article. Review.
Arrhythmogenic right ventricular cardiomyopathy (ARVC) encompasses a group of conditions characterized by right ventricular fibrofatty infiltration, with a predominant arrhythmic presentation. First described in the late 1970s and early 1980s, i
Arrhythmogenic right ventricular cardiomyopathy (ARVC) encompasses a group of conditions characterized by right
Cardiomyopathies in children: An overview.
Tsatsopoulou A, Protonotarios I, Xylouri Z, Papagiannis I, Anastasakis A, Germanakis I, Patrianakos A, Nyktari E, Gavras C, Papadopoulos G, Meditskou S, Lazarou E, Miliou A, Lazaros G. Tsatsopoulou A, et al. Hellenic J Cardiol. 2023 Jul-Aug;72:43-56. doi: 10.1016/j.hjc.2023.02.007. Epub 2023 Mar 3. Hellenic J Cardiol. 2023. PMID: 36870438 Free article. Review.
Arrhythmogenic right ventricular cardiomyopathy (ARVC), restrictive cardiomyopathy, and left ventricular noncompaction are less commonly diagnosed. ...Acute myocarditis in children has an incidence of 1.4-2.1 cases/per 100,000 children pe
Arrhythmogenic right ventricular cardiomyopathy (ARVC), restrictive cardiomyopathy, and left ventricular noncomp
[Canalopathies, arrhythmogenic right ventricular cardiomyopathy and artefacts].
Brüggemann B, Djajadisastra I, Duncker D, Eitel C, Fink T, Grimm W, Heeger C, Israel CW, Müller-Leisse J, Sheta MK, Sinha AM, Tilz RR, Veltmann C, Vogler J, Zormpas C. Brüggemann B, et al. Herzschrittmacherther Elektrophysiol. 2019 Mar;30(1):51-71. doi: 10.1007/s00399-019-0611-5. Epub 2019 Mar 1. Herzschrittmacherther Elektrophysiol. 2019. PMID: 30825043 Review. German. No abstract available.
Arrhythmogenic right ventricular dysplasia/cardiomyopathy.
Fontaine G, Gallais Y, Fornes P, Hébert JL, Frank R. Fontaine G, et al. Anesthesiology. 2001 Jul;95(1):250-4. doi: 10.1097/00000542-200107000-00035. Anesthesiology. 2001. PMID: 11465564 Review. No abstract available.
Hereditary Syndromes of Sudden Cardiac Death.
Berberian JG. Berberian JG. Emerg Med Clin North Am. 2022 Nov;40(4):651-662. doi: 10.1016/j.emc.2022.06.005. Epub 2022 Oct 7. Emerg Med Clin North Am. 2022. PMID: 36396213 Review.
Sudden cardiac death (SCD) describes the unexpected natural death from a cardiac cause within a short time period, generally 1 hour or lesser from the onset of symptoms, often due to a cardiac dysrhythmia. Overall, the most common cause of SCD is coronary artery disease bu …
Sudden cardiac death (SCD) describes the unexpected natural death from a cardiac cause within a short time period, generally 1 hour o …
Pathogenesis of arrhythmogenic cardiomyopathy: role of inflammation.
Lin YN, Ibrahim A, Marbán E, Cingolani E. Lin YN, et al. Basic Res Cardiol. 2021 Jun 4;116(1):39. doi: 10.1007/s00395-021-00877-5. Basic Res Cardiol. 2021. PMID: 34089132 Review.
Arrhythmogenic cardiomyopathy (AC) is an inherited disease characterized by progressive breakdown of heart muscle, myocardial tissue death, and fibrofatty replacement. ...
Arrhythmogenic cardiomyopathy (AC) is an inherited disease characterized by progressive breakdown of heart muscle, myocardial tissue
Differential diagnosis of rSr' pattern in leads V1 -V2. Comprehensive review and proposed algorithm.
Baranchuk A, Enriquez A, García-Niebla J, Bayés-Genís A, Villuendas R, Bayés de Luna A. Baranchuk A, et al. Ann Noninvasive Electrocardiol. 2015 Jan;20(1):7-17. doi: 10.1111/anec.12241. Epub 2014 Dec 26. Ann Noninvasive Electrocardiol. 2015. PMID: 25546557 Free PMC article. Review.
We often face this finding in asymptomatic and otherwise healthy individuals and the causes may vary from benign nonpathological variants to severe or life-threatening heart diseases, such as Brugada syndrome or arrhythmogenic right ventricular dysplasia
We often face this finding in asymptomatic and otherwise healthy individuals and the causes may vary from benign nonpathological variants to …
Arrhythmogenic right ventricular dysplasia/cardiomyopathy: an electrocardiogram-based review.
Nunes de Alencar Neto J, Baranchuk A, Bayés-Genís A, Bayés de Luna A. Nunes de Alencar Neto J, et al. Europace. 2018 Jun 1;20(FI1):f3-f12. doi: 10.1093/europace/eux202. Europace. 2018. PMID: 29272363 Review.
Arrhythmogenic right ventricular dysplasia or cardiomyopathy (ARVD/C) is a pathologic condition where the right ventricle is partially or totally replaced by fatty and fibrous tissue. ...More common ventricular arrhythmias and risk of sud
Arrhythmogenic right ventricular dysplasia or cardiomyopathy (ARVD/C) is a pathologic condition where the rig
172 results