Molecular disturbance underlies to arrhythmogenic cardiomyopathy induced by transgene content, age and exercise in a truncated PKP2 mouse model
J Moncayo-Arlandi, E Guasch… - Human Molecular …, 2016 - academic.oup.com
Arrhythmogenic cardiomyopathy (ACM) is a disorder characterized by a progressive
ventricular myocardial replacement by fat and fibrosis, which lead to ventricular arrhythmias …
ventricular myocardial replacement by fat and fibrosis, which lead to ventricular arrhythmias …
[HTML][HTML] Explaining the Unexplained: A Practical Approach to Investigating the Cardiac Arrest Survivor
G Suna, GJ Mellor - Arrhythmia & electrophysiology review, 2023 - ncbi.nlm.nih.gov
Sudden cardiac arrest (SCA) is a common cause of death. The majority of SCA is caused by
ventricular arrhythmia due to underlying CHD. Aborted SCA with no apparent diagnosis after …
ventricular arrhythmia due to underlying CHD. Aborted SCA with no apparent diagnosis after …
Left ventricular dysfunction in arrhythmogenic cardiomyopathy: association with exercise exposure, genetic basis, and prognosis
ØH Lie, M Chivulescu… - Journal of the …, 2021 - Am Heart Assoc
Background Arrhythmogenic cardiomyopathy (AC) is characterized by biventricular
dysfunction, exercise intolerance, and high risk of ventricular tachyarrhythmias and sudden …
dysfunction, exercise intolerance, and high risk of ventricular tachyarrhythmias and sudden …
[HTML][HTML] Inherited cardiomyopathies and sports participation
Competitive sports activity is associated with an increased risk of sudden cardiovascular
death in adolescents and young adults with inherited cardiomyopathies. Many young …
death in adolescents and young adults with inherited cardiomyopathies. Many young …
[HTML][HTML] Facts and gaps in exercise influence on arrhythmogenic cardiomyopathy: new insights from a meta-analysis approach
J Martínez-Solé, M Sabater-Molina… - Frontiers in …, 2021 - frontiersin.org
Arrhythmogenic cardiomyopathy (ACM) is a genetic cardiac condition characterized by
fibrofatty myocardial replacement, either at the right ventricle, at the left ventricle, or with …
fibrofatty myocardial replacement, either at the right ventricle, at the left ventricle, or with …
Second hits in dilated cardiomyopathy
P Marstrand, K Picard, NK Lakdawala - Current Cardiology Reports, 2020 - Springer
Abstract Purpose of Review Genetic studies have identified an increasing number of culprit
disease genes in patients with dilated cardiomyopathy (DCM). While these studies were …
disease genes in patients with dilated cardiomyopathy (DCM). While these studies were …
Arrhythmogenic cardiomyopathy and sports activity
A Zorzi, A Cipriani, G Mattesi, R Vio, N Bettella… - Journal of …, 2020 - Springer
Arrhythmogenic right-ventricular cardiomyopathy (ARVC) is a genetically determined heart
disease characterized by progressive myocyte death and substitution by fibrofatty tissue. Life …
disease characterized by progressive myocyte death and substitution by fibrofatty tissue. Life …
Medico-legal perspectives on sudden cardiac death in young athletes
Sudden cardiac death (SCD) in a young athlete represents a dramatic event, and an
increasing number of medico-legal cases have addressed this topic. In addition to …
increasing number of medico-legal cases have addressed this topic. In addition to …
Arrhythmogenic right ventricular cardiomyopathy: progress toward personalized management
Arrhythmogenic right ventricular cardiomyopathy (ARVC) is an inherited heart disease
characterized by fibrofatty replacement of the ventricular myocardium, a high risk of …
characterized by fibrofatty replacement of the ventricular myocardium, a high risk of …
Utility of genetic testing in athletes
B Gray, C Semsarian - Clinical Cardiology, 2020 - Wiley Online Library
Athletes are some of the fittest members of our society, yet paradoxically carry an increased
risk of sudden cardiac death (SCD). The athlete's underlying risk of SCD in sports may be …
risk of sudden cardiac death (SCD). The athlete's underlying risk of SCD in sports may be …