Arrhythmogenic right ventricular cardiomyopathy/dysplasia (ARVC/D) in clinical practice

KHC Li, G Bazoukis, T Liu, G Li, WKK Wu… - Journal of …, 2018 - Wiley Online Library
Arrhythmogenic right ventricular cardiomyopathy/dysplasia (ARVC/D) is an inherited
myocardial disease characterized by fibro‐fatty replacement of the right ventricular …

[HTML][HTML] Всероссийские клинические рекомендации по контролю над риском внезапной остановки сердца и внезапной сердечной смерти, профилактике и …

АШ Ревишвили, НМ Неминущий… - Вестник …, 2017 - vestar.elpub.ru
внезапная смерть, внезапная сердечная смерть, врожденный порок сердца,
дефибриллятор, рекомендации, сердечная недостаточность, имплантируемый …

Cardiac magnetic resonance based deformation imaging: role of feature tracking in athletes with suspected arrhythmogenic right ventricular cardiomyopathy

C Czimbalmos, I Csecs, Z Dohy, A Toth… - The international journal …, 2019 - Springer
Both, arrhythmogenic right ventricular cardiomyopathy (ARVC) and regular training are
associated with right ventricular (RV) remodelling. Cardiac magnetic resonance (CMR) is …

[HTML][HTML] Exercise-induced right ventricular injury or arrhythmogenic cardiomyopathy (ACM): The bright side and the dark side of the moon

R Leischik, B Dworrak, M Strauss, M Horlitz… - Progress in …, 2020 - Elsevier
There is still debate on the range of normal physiologic changes of the right ventricle or
ventricular (RV) function in athletes. Genetic links to arrhythmogenic cardiomyopathy (ACM) …

[HTML][HTML] Arrhythmogenic right ventricular cardiomyopathy/dysplasia: an updated review of diagnosis and management

Y Sattar, HM Abdullah, EN Samani, M Myla, W Ullah - Cureus, 2019 - ncbi.nlm.nih.gov
Arrhythmogenic right ventricular cardiomyopathy/dysplasia (ARVC/D) is a condition caused
by the replacement of the normal right ventricular myocardium with fibrofatty tissue. ARVC/D …

Exercise and arrhythmic risk in TMEM43 p. S358L arrhythmogenic right ventricular cardiomyopathy

FL Paulin, KA Hodgkinson, S MacLaughlan… - Heart Rhythm, 2020 - Elsevier
Background High-level exercise has been associated with a malignant phenotype in
desmosomal and genotype-negative forms of arrhythmogenic right ventricular …

Arrhythmogenic Cardiomyopathy: from Preclinical Models to Genotype–phenotype Correlation and Pathophysiology

X Fan, G Yang, F Duru, M Grilli, I Akin, X Zhou… - Stem Cell Reviews and …, 2023 - Springer
Arrhythmogenic cardiomyopathy (ACM) is a hereditary myocardial disease characterized by
the replacement of the ventricular myocardium with fibrous fatty deposits. ACM is usually …

Exercise is associated with impaired left ventricular systolic function in patients with lamin A/C genotype

ET Skjølsvik, NE Hasselberg, LA Dejgaard… - Journal of the …, 2020 - Am Heart Assoc
Background Lamin A/C cardiomyopathy is a malignant and highly penetrant inheritable
cardiomyopathy. Competitive sports have been associated with adverse events in these …

Integrating exercise into personalized ventricular arrhythmia risk prediction in arrhythmogenic right ventricular cardiomyopathy

LP Bosman, W Wang, ØH Lie… - Circulation …, 2022 - Am Heart Assoc
Background: Exercise is associated with sustained ventricular arrhythmias (VA) in
Arrhythmogenic Right Ventricular Cardiomyopathy (ARVC) but is not included in the ARVC …

Evolving spectrum of arrhythmogenic cardiomyopathy: Implications for Sports Cardiology

F Graziano, A Cipriani, D Balla, S Bondarev… - Clinical …, 2023 - Wiley Online Library
Arrhythmogenic cardiomyopathy (ACM) is a genetic heart muscle disease, structurally
characterized by progressive fibro‐fatty replacement of the normal myocardium and …