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1997
2025

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

Year Number of Results
1997 1
2000 2
2003 1
2004 3
2005 2
2006 2
2010 2
2011 1
2014 4
2015 3
2016 1
2017 3
2018 2
2019 3
2020 3
2021 1
2022 2
2023 4
2024 4
2025 0

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38 results

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Page 1
Diagnosis of Arrhythmogenic Right Ventricular Cardiomyopathy: Progress and Pitfalls.
Oomen AWGJ, Semsarian C, Puranik R, Sy RW. Oomen AWGJ, et al. Heart Lung Circ. 2018 Nov;27(11):1310-1317. doi: 10.1016/j.hlc.2018.03.023. Epub 2018 Apr 4. Heart Lung Circ. 2018. PMID: 29705385 Review.
Arrhythmogenic right ventricular cardiomyopathy (ARVC) is an inherited cardiomyopathy that predominantly affects the right ventricle. ...There is no single pathognomonic diagnostic finding in ARVC; rather, current international task force criteria spec
Arrhythmogenic right ventricular cardiomyopathy (ARVC) is an inherited cardiomyopathy that predominantly affects the
The pivotal role of compelling high-risk electrocardiographic markers in prediction of ventricular arrhythmic risk in arrhythmogenic right ventricular cardiomyopathy: A systematic review and meta-analysis.
Iqbal M, Kamarullah W, Achmad C, Karwiky G, Akbar MR. Iqbal M, et al. Curr Probl Cardiol. 2024 Feb;49(2):102241. doi: 10.1016/j.cpcardiol.2023.102241. Epub 2023 Nov 29. Curr Probl Cardiol. 2024. PMID: 38040211 Free article. Review.
INTRODUCTION: Several investigations have shown that existing risk stratification processes remain insufficient for stratifying sudden cardiac death risk in arrhythmogenic right ventricular cardiomyopathy (ARVC). Multiple auxiliary parameters are investigated …
INTRODUCTION: Several investigations have shown that existing risk stratification processes remain insufficient for stratifying sudden cardi …
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
Pathogenesis of Arrhythmogenic Cardiomyopathy.
Asimaki A, Kleber AG, Saffitz JE. Asimaki A, et al. Can J Cardiol. 2015 Nov;31(11):1313-24. doi: 10.1016/j.cjca.2015.04.012. Epub 2015 Apr 24. Can J Cardiol. 2015. PMID: 26199027 Free PMC article. Review.
Arrhythmogenic cardiomyopathy (ACM) is a primary myocardial disease. It is characterized by frequent ventricular arrhythmias and increased risk of sudden cardiac death typically arising as an early manifestation before the onset of significant myocardial remodelling
Arrhythmogenic cardiomyopathy (ACM) is a primary myocardial disease. It is characterized by frequent ventricular arrhythmias a
Basic and translational mechanisms in inflammatory arrhythmogenic cardiomyopathy.
Engel M, Shiel EA, Chelko SP. Engel M, et al. Int J Cardiol. 2024 Feb 15;397:131602. doi: 10.1016/j.ijcard.2023.131602. Epub 2023 Nov 17. Int J Cardiol. 2024. PMID: 37979796 Review.
That said, of the five desmosomal genes implicated in ACM, pathogenic variants in desmocollin-2 (DSC2) and desmoglein-2 (DSG2) have been discovered in both an autosomal-recessive and autosomal-dominant pattern (Wong et al., [4]; Qadri et al., [5]; Chen et al., [6]). Originally kn …
That said, of the five desmosomal genes implicated in ACM, pathogenic variants in desmocollin-2 (DSC2) and desmoglein-2 (DSG2) have been dis …
Naxos disease - a narrative review.
Leopoulou M, Mattsson G, LeQuang JA, Pergolizzi JV, Varrassi G, Wallhagen M, Magnusson P. Leopoulou M, et al. Expert Rev Cardiovasc Ther. 2020 Nov;18(11):801-808. doi: 10.1080/14779072.2020.1828064. Epub 2020 Oct 8. Expert Rev Cardiovasc Ther. 2020. PMID: 32966140 Review.
There is an increased risk of arrhythmias, including sudden cardiac death at a young age. Right ventricular systolic dysfunction often progresses and left ventricular involvement may also occur. ...EXPERT OPINION: The principles of evaluation and treatment ar …
There is an increased risk of arrhythmias, including sudden cardiac death at a young age. Right ventricular systolic dysfuncti …
Arrhythmogenic right ventricular cardiomyopathies: Diagnostic challenges from imaging to genetics.
Casian M, Papadakis M, Jurcut R. Casian M, et al. Kardiol Pol. 2024;82(11):1059-1070. doi: 10.33963/v.phj.102391. Epub 2024 Sep 6. Kardiol Pol. 2024. PMID: 39240923 Free article. Review.
Arrhythmogenic right ventricular cardiomyopathy (ARVC) is a hereditary cardiomyopathy, predominantly affecting young males, regardless of their ethnicity. ...
Arrhythmogenic right ventricular cardiomyopathy (ARVC) is a hereditary cardiomyopathy, predominantly affecting young ma
Insights Into Genetics and Pathophysiology of Arrhythmogenic Cardiomyopathy.
Gerull B, Brodehl A. Gerull B, et al. Curr Heart Fail Rep. 2021 Dec;18(6):378-390. doi: 10.1007/s11897-021-00532-z. Epub 2021 Sep 3. Curr Heart Fail Rep. 2021. PMID: 34478111 Free PMC article. Review.
PURPOSE OF REVIEW: Arrhythmogenic cardiomyopathy (ACM) is a genetic disease characterized by life-threatening ventricular arrhythmias and sudden cardiac death (SCD) in apparently healthy young adults. ...
PURPOSE OF REVIEW: Arrhythmogenic cardiomyopathy (ACM) is a genetic disease characterized by life-threatening ventricular arrh …
Arrhythmogenic right ventricular cardiomyopathy/dysplasia: is there a role for viruses?
Calabrese F, Basso C, Carturan E, Valente M, Thiene G. Calabrese F, et al. Cardiovasc Pathol. 2006 Jan-Feb;15(1):11-7. doi: 10.1016/j.carpath.2005.10.004. Cardiovasc Pathol. 2006. PMID: 16414451 Review.
Arrhythmogenic right ventricular cardiomyopathy/dysplasia (ARVC/D) is a primary heart muscle disease characterized structurally by progressive fibrofatty replacement of the right ventricle and clinically by life-threatening ventricular ar
Arrhythmogenic right ventricular cardiomyopathy/dysplasia (ARVC/D) is a primary heart muscle disease characteriz
From Hypertrophy to Heart Failure: What Is New in Genetic Cardiomyopathies.
Reza N, Musunuru K, Owens AT. Reza N, et al. Curr Heart Fail Rep. 2019 Oct;16(5):157-167. doi: 10.1007/s11897-019-00435-0. Curr Heart Fail Rep. 2019. PMID: 31243690 Free PMC article. Review.
PURPOSE: The purpose of this review is to provide an update on the recent advances in the research and clinical care of patients with the major phenotypes of inherited cardiomyopathies-hypertrophic, dilated, and arrhythmogenic. Developments in genetics, risk stratification …
PURPOSE: The purpose of this review is to provide an update on the recent advances in the research and clinical care of patients with the ma …
38 results