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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 2

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36 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 …
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 …
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 …
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 …
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 …
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 …
Variant Location Is a Novel Risk Factor for Individuals With Arrhythmogenic Cardiomyopathy Due to a Desmoplakin (DSP) Truncating Variant.
Hoorntje ET, Burns C, Marsili L, Corden B, Parikh VN, Te Meerman GJ, Gray B, Adiyaman A, Bagnall RD, Barge-Schaapveld DQCM, van den Berg MP, Bootsma M, Bosman LP, Correnti G, Duflou J, Eppinga RN, Fatkin D, Fietz M, Haan E, Jongbloed JDH, Hauer AD, Lam L, van Lint FHM, Lota A, Marcelis C, McCarthy HJ, van Mil AM, Oldenburg RA, Pachter N, Planken RN, Reuter C, Semsarian C, van der Smagt JJ, Thompson T, Vohra J, Volders PGA, van Waning JI, Whiffin N, van den Wijngaard A, Amin AS, Wilde AAM, van Woerden G, Yeates L, Zentner D, Ashley EA, Wheeler MT, Ware JS, van Tintelen JP, Ingles J. Hoorntje ET, et al. Circ Genom Precis Med. 2023 Feb;16(1):e003672. doi: 10.1161/CIRCGEN.121.003672. Epub 2022 Dec 29. Circ Genom Precis Med. 2023. PMID: 36580316 Free PMC article. Review.
We evaluated phenotype, risk factors for ventricular arrhythmias, and underlying genetics of DSPtv cardiomyopathy. ...RESULTS: There were 98 probands and 72 family members (mean age at diagnosis 438 years, 59% women) with a DSPtv, of which 146 were considered clinically af …
We evaluated phenotype, risk factors for ventricular arrhythmias, and underlying genetics of DSPtv cardiomyopathy. ...RESULTS: There …
Diagnostic Differentiation Between Arrhythmogenic Cardiomyopathy and Athlete's Heart by Using Imaging.
D'Ascenzi F, Solari M, Corrado D, Zorzi A, Mondillo S. D'Ascenzi F, et al. JACC Cardiovasc Imaging. 2018 Sep;11(9):1327-1339. doi: 10.1016/j.jcmg.2018.04.031. JACC Cardiovasc Imaging. 2018. PMID: 30190032 Free article. Review.
Arrhythmogenic right ventricular cardiomyopathy (ARVC) is an important cause of sudden cardiac death (SCD) in youth and athletes. In the last decade, several studies focused on right ventricular (RV) remodeling in athletes and revealed that feat …
Arrhythmogenic right ventricular cardiomyopathy (ARVC) is an important cause of sudden cardiac death (SCD) in youth and …
[Diagnosis and therapy of arrhythmogenic right ventricular cardiomyopathy].
Zorzi A, Rigato I, Migliore F, Perazzolo Marra M, Basso C, Thiene G, Bauce B, Corrado D. Zorzi A, et al. G Ital Cardiol (Rome). 2014 Nov;15(11):616-25. doi: 10.1714/1694.18506. G Ital Cardiol (Rome). 2014. PMID: 25424140 Review. Italian.
Arrhythmogenic right ventricular cardiomyopathy (ARVC) is an inherited heart muscle disease that predisposes to the occurrence of ventricular arrhythmias and sudden death, particularly in the young and athlete. The classic variant of the disease predom …
Arrhythmogenic right ventricular cardiomyopathy (ARVC) is an inherited heart muscle disease that predisposes to the occ …
36 results