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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
1991 2
1995 3
1996 3
1997 1
1998 2
1999 2
2000 2
2001 3
2002 3
2003 5
2004 4
2005 11
2006 4
2007 5
2008 9
2009 12
2010 4
2011 5
2012 8
2013 2
2014 9
2015 10
2016 8
2017 12
2018 7
2019 5
2020 6
2021 5
2022 9
2023 4
2024 3
2025 0

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155 results

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Page 1
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
Cardiomyopathy and pregnancy.
Schaufelberger M. Schaufelberger M. Heart. 2019 Oct;105(20):1543-1551. doi: 10.1136/heartjnl-2018-313476. Epub 2019 Jul 15. Heart. 2019. PMID: 31308064 Free PMC article. Review.
The most common cardiomyopathies are hypertrophic and dilated cardiomyopathy. Rare types are arrhythmogenic right ventricular, restrictive, Takotsubo and left ventricular non-compaction cardiomyopathies. ...Complications include different types of supr …
The most common cardiomyopathies are hypertrophic and dilated cardiomyopathy. Rare types are arrhythmogenic right ventricul
Arrhythmogenic right ventricular cardiomyopathy: a focused update on diagnosis and risk stratification.
Bosman LP, Te Riele ASJM. Bosman LP, et al. Heart. 2022 Jan;108(2):90-97. doi: 10.1136/heartjnl-2021-319113. Epub 2021 May 14. Heart. 2022. PMID: 33990412 Review.
Arrhythmogenic right ventricular cardiomyopathy (ARVC) is an inherited cardiomyopathy characterised by fibrofatty replacement of predominantly the right ventricle and high risk of ventricular arrhythmias and sudden cardiac death (SCD). ...Adding
Arrhythmogenic right ventricular cardiomyopathy (ARVC) is an inherited cardiomyopathy characterised by fibrofatty repla
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.
Dilated and hypertrophic cardiomyopathy phenotypes share an incidence of 60% and 25%, respectively. Arrhythmogenic right ventricular cardiomyopathy (ARVC), restrictive cardiomyopathy, and left ventricular noncompaction are less commonly diagnosed. ...A …
Dilated and hypertrophic cardiomyopathy phenotypes share an incidence of 60% and 25%, respectively. Arrhythmogenic right ve
Relationship between arrhythmogenic right ventricular dysplasia and exercise.
Sawant AC, Calkins H. Sawant AC, et al. Card Electrophysiol Clin. 2015 Jun;7(2):195-206. doi: 10.1016/j.ccep.2015.03.004. Epub 2015 Apr 8. Card Electrophysiol Clin. 2015. PMID: 26002386 Review.
Arrhythmogenic right ventricular dysplasia/cardiomyopathy (ARVD/C) is rare cardiomyopathy associated with life-threatening arrhythmias and increased risk of sudden cardiac death. ...
Arrhythmogenic right ventricular dysplasia/cardiomyopathy (ARVD/C) is rare cardiomyopathy associated with life-t
Arrhythmogenic Cardiomyopathy and Sports Activity.
Zorzi A, Cipriani A, Mattesi G, Vio R, Bettella N, Corrado D. Zorzi A, et al. J Cardiovasc Transl Res. 2020 Jun;13(3):274-283. doi: 10.1007/s12265-020-09995-2. Epub 2020 Apr 16. J Cardiovasc Transl Res. 2020. PMID: 32300932 Review.
Arrhythmogenic right-ventricular cardiomyopathy (ARVC) is a genetically determined heart disease characterized by progressive myocyte death and substitution by fibrofatty tissue. Life-threatening ventricular arrhythmias may occur during the course of t
Arrhythmogenic right-ventricular cardiomyopathy (ARVC) is a genetically determined heart disease characterized by progr
Treatment of arrhythmogenic right ventricular cardiomyopathy/dysplasia: an international task force consensus statement.
Corrado D, Wichter T, Link MS, Hauer R, Marchlinski F, Anastasakis A, Bauce B, Basso C, Brunckhorst C, Tsatsopoulou A, Tandri H, Paul M, Schmied C, Pelliccia A, Duru F, Protonotarios N, Estes NA 3rd, McKenna WJ, Thiene G, Marcus FI, Calkins H. Corrado D, et al. Eur Heart J. 2015 Dec 7;36(46):3227-37. doi: 10.1093/eurheartj/ehv162. Epub 2015 Jul 27. Eur Heart J. 2015. PMID: 26216920 Free PMC article. Review. No abstract available.
[Monogenic heart disease].
Schönberger J, Ertl G. Schönberger J, et al. Med Klin (Munich). 2008 Mar 15;103(3):166-74. doi: 10.1007/s00063-008-1024-0. Med Klin (Munich). 2008. PMID: 18344067 Review. German.
Diagnostic Criteria, Genetics, and Molecular Basis of Arrhythmogenic Cardiomyopathy.
Basso C, Pilichou K, Bauce B, Corrado D, Thiene G. Basso C, et al. Heart Fail Clin. 2018 Apr;14(2):201-213. doi: 10.1016/j.hfc.2018.01.002. Heart Fail Clin. 2018. PMID: 29525648 Review.
Arrhythmogenic cardiomyopathy (AC) is an inherited heart muscle disease characterized by myocardial atrophy and fibrofatty replacement of the ventricular myocardium, at risk of sudden cardiac death, particularly in the young and athletes. ...
Arrhythmogenic cardiomyopathy (AC) is an inherited heart muscle disease characterized by myocardial atrophy and fibrofatty replacemen
155 results