Arrhythmogenic cardiomyopathy
D Corrado, C Basso, DP Judge - Circulation research, 2017 - Am Heart Assoc
Arrhythmogenic cardiomyopathy is an inherited heart muscle disorder, predisposing to
sudden cardiac death, particularly in young patients and athletes. Pathological features …
sudden cardiac death, particularly in young patients and athletes. Pathological features …
Molecular mechanisms of arrhythmogenic cardiomyopathy
KM Austin, MA Trembley, SF Chandler… - Nature Reviews …, 2019 - nature.com
Arrhythmogenic cardiomyopathy is a genetic disorder characterized by the risk of life-
threatening arrhythmias, myocardial dysfunction and fibrofatty replacement of myocardial …
threatening arrhythmias, myocardial dysfunction and fibrofatty replacement of myocardial …
Arrhythmogenic right ventricular cardiomyopathy
Arrhythmogenic right ventricular cardiomyopathy is a rare inherited heart-muscle disease
that is a cause of sudden death in young people and athletes. Causative mutations in genes …
that is a cause of sudden death in young people and athletes. Causative mutations in genes …
Identification of mutations in the cardiac ryanodine receptor gene in families affected with arrhythmogenic right ventricular cardiomyopathy type 2 (ARVD2)
N Tiso, DA Stephan, A Nava, A Bagattin… - Human molecular …, 2001 - academic.oup.com
Arrhythmogenic right ventricular dysplasia type 2 (ARVD2, OMIM 600996) is an autosomal
dominant cardiomyopathy, characterized by partial degeneration of the myocardium of the …
dominant cardiomyopathy, characterized by partial degeneration of the myocardium of the …
Clinical profile and long-term follow-up of 37 families with arrhythmogenic right ventricular cardiomyopathy
A Nava, B Bauce, C Basso, M Muriago… - Journal of the American …, 2000 - jacc.org
OBJECTIVES We sought to define the clinical picture and natural history of familial
arrhythmogenic right ventricular cardiomyopathy (ARVC). BACKGROUND Arrhythmogenic …
arrhythmogenic right ventricular cardiomyopathy (ARVC). BACKGROUND Arrhythmogenic …
Compound and digenic heterozygosity predicts lifetime arrhythmic outcome and sudden cardiac death in desmosomal gene–related arrhythmogenic right ventricular …
I Rigato, B Bauce, A Rampazzo, A Zorzi… - Circulation …, 2013 - Am Heart Assoc
Background—Mutations in genes encoding for desmosomal proteins are the most common
cause of arrhythmogenic right ventricular cardiomyopathy (ARVC). We assessed the value …
cause of arrhythmogenic right ventricular cardiomyopathy (ARVC). We assessed the value …
Sudden cardiac death in young people with apparently normal heart
Objective: The aim of the present study was to assess the prevalence of subtle morphologic
substrates, clinically unrecognizable, underlying sudden cardiac death (SCD) in young …
substrates, clinically unrecognizable, underlying sudden cardiac death (SCD) in young …
Postmortem diagnosis in sudden cardiac death victims: macroscopic, microscopic and molecular findings
C Basso, F Calabrese, D Corrado… - Cardiovascular …, 2001 - academic.oup.com
1. Introduction autopsy reports [13]. When focusing the attention only on young athletes the
prevalence was twice that in young non When sudden death (SD) occurs in adults and …
prevalence was twice that in young non When sudden death (SD) occurs in adults and …
Cardiac histological substrate in patients with clinical phenotype of Brugada syndrome
Background—The role of structural heart disease and sodium channel dysfunction in the
induction of electrical instability in Brugada syndrome is still debated. Methods and Results …
induction of electrical instability in Brugada syndrome is still debated. Methods and Results …
Arrhythmogenic cardiomyopathy
K Pilichou, G Thiene, B Bauce, I Rigato… - Orphanet journal of rare …, 2016 - Springer
Arrhythmogenic cardiomyopathy (AC) is a heart muscle disease clinically characterized by
life-threatening ventricular arrhythmias and pathologically by an acquired and progressive …
life-threatening ventricular arrhythmias and pathologically by an acquired and progressive …