• The specific situation of the patient. Unless otherwise provided for by national regulations,
off-label use of medication should be limited to situations where it is in the patient's interest …

Cardiomyopathies, arrhythmic syndromes, aortopathies, and other cardiovascular diseases
with Mendelian inheritance are relatively frequent conditions for which genetic testing is …

Objectives: The aim of this study was to examine the characteristics of non-sustained
ventricular tachycardia (NSVT) episodes during Holter monitoring and to determine their …

Aims Left ventricular outflow tract obstruction (LVOTO) is associated with reduced survival in
patients with hypertrophic cardiomyopathy (HCM). The influence of LVOTO on survival from …

Restrictive cardiomyopathy (RCM) is an uncommon heart muscle disorder characterized by
impaired filling of the ventricles with reduced volume in the presence of normal or near …

Objectives: We sought to ascertain the prevalence and mode of expression of familial
disease in a consecutive series of patients with arrhythmogenic right ventricular …

Objective: To determine the range of survival rates of patients with hypertrophic
cardiomyopathy (HCM) by comparing and contrasting the natural history of a cohort of …

Left ventricular noncompaction (LVNC) causes prominent ventricular trabeculations and
reduces cardiac systolic function. The clinical presentation of LVNC ranges from …

Objectives: The purpose of this study was to determine the prevalence, clinical significance,
and genetic basis of hypertrophic cardiomyopathy (HCM) with “restrictive phenotype” …

Brugada syndrome (BrS) is a cardiac arrhythmia disorder associated with sudden death in
young adults. With the exception of SCN5A, encoding the cardiac sodium channel NaV1. 5 …