Functional Effects of the TMEM43 Ser358Leu Mutation in the Pathogenesis of Arrhythmogenic Right Ventricular Cardiomyopathy [PDF]
, 2012 Background: The Ser358Leu mutation in TMEM43, encoding an inner nuclear membrane protein, has been implicated in arrhythmogenic right ventricular cardiomyopathy (ARVC). The pathogenetic mechanisms of this mutation are poorly understood.
Ahmad, Ferhaan +4 more
core +5 more sources
Atrial tachycardia in a patient with arrhythmogenic right ventricular cardiomyopathy/dysplasia
Journal of Arrhythmia, 2013 We describe a 49-year-old woman with atrial tachycardia (AT) and arrhythmogenic right ventricular cardiomyopathy/dysplasia. Cardiac magnetic resonance images showed a markedly dilated right atrium and right ventricle.
Hiroaki Mano +11 more
doaj +1 more source
Alternative Lead ECG Placements
Annals of Noninvasive Electrocardiology, Volume 31, Issue 3, May 2026.Alternative ECG lead placements can improve diagnostic yield when the standard 12‐lead ECG is suboptimal or infeasible. This review summarizes practical, scenario‐driven modifications (right‐sided, posterior, seated/prone, Lewis, Fontaine, torso‐based, and monitoring configurations) to better detect ischemia, right ventricular disease/ARVD, and ...
José Luis Morales‐Arteaga +12 more
wiley +1 more source
Sudden cardiac death in inherited cardiomyopathy [PDF]
, 2017 Cardiomyopathy is an important cause of sudden cardiac death particularly in adolescents and young adults. The risk of sudden cardiac death varies between individual cardiomyopathies and is dependent on the severity of disease, age and gender.
Collis, R, Elliott, PM
core +1 more source
SORBS2: A Molecular Nexus in Multisystem Diseases Through Scaffold‐Mediated Regulation
Journal of Cellular and Molecular Medicine, Volume 30, Issue 9, May 2026.ABSTRACT Sorbin and SH3 Domain Containing 2 (SORBS2), a multifunctional scaffold protein harbouring Sorbin homology (SoHo) and Src homology 3 (SH3) domains, serves as a molecular hub in human diseases by integrating cytoskeletal remodelling, signal transduction and RNA metabolic regulation. This study systematically analyses SORBS2's molecular features,
Qiwei Jia, Yong Zhang
wiley +1 more source
Therapeutic management in Sicilian patients with definite arrhythmogenic right ventricular dysplasia/cardiomyopathy and focus on the role of implantable cardioverter-defibrillator therapy [PDF]
, 2014 No abstract ...
Arrotti, S +11 more
core +1 more source
Atypical case of post-partum cardiomyopathy: an overlap syndrome with arrhythmogenic right ventricular cardiomyopathy? [PDF]
, 2015 A middle-aged female patient presented with increasing dyspnoea following delivery of her second child. Echocardiography showed left ventricular (LV) dilatation and severe global impairment of systolic function (ejection fraction < 10%) but normal right ...
Ali, A +4 more
core +1 more source
Folia CardiologicaArrhythmogenic right ventricular cardiomyopathy (ARVC) is a genetically predisposed form of cardiomyopathy. The pathogenesis of ARVC involves structural and functional changes in the myocardium, particularly in the right ventricle, leading to its ...
Alexander Suchodolski +5 more
doaj +1 more source
An unusual case of sudden cardiac death during sexual intercourse [PDF]
, 2018 The most common cause of sudden death during sexual intercourse in adults is heart disease, and it is usually the male, whereas the death of the woman is unusual. Generally, in these cases, death occurs as a result of cardiovascular disease.
Argo, Antonina +5 more
core +1 more source
Radiology Case ReportsArrhythmogenic right ventricular cardiomyopathy (ARVC) is a rare myocardial genetic disease that leads to heart failure and sudden cardiac death. The diagnosis of ARVC remains challenging given its variable presentation.
Manal Msirdi +4 more
doaj +1 more source