Cardiovascular genetics is a rapidly evolving subspecialty within cardiovascular medicine,
and its growth is attributed to advances in genome sequencing and genetic testing and the …

Catecholaminergic polymorphic ventricular tachycardia is a rare devastating lethal inherited
disorder or sporadic cardiac ion channelopathy characterized by unexplained syncopal …

The diffusion of next-generation sequencing (NGS)-based approaches allows for the
identification of pathogenic mutations of cardiomyopathies and channelopathies in more …

Cardiac arrhythmias remain a common challenge and are associated with significant
morbidity and mortality. Effective and safe rhythm control strategies are a primary, yet unmet …

Ion channels are membrane-spanning integral proteins expressed in multiple organs,
including the eye. In the eye, ion channels are involved in various physiological processes …

Abstract Introduction Long QT syndrome (LQTS) is a life‐threatening inherited
channelopathy, and prolonged QT intervals easily trigger malignant arrhythmias, especially …

Background Genetic diagnostics support the diagnosis of hereditary arrhythmogenic
diseases, but variants of uncertain significance (VUS) complicate matters, emphasising the …

Intense athletic training and competition can rarely result in sudden cardiac death (SCD).
Despite the introduction of pre-participation cardiovascular screening, especially among …

Ventricular rhythms are abnormal rhythms arising from the ventricles. They are among the
most clinically relevant arrhythmias for their potential to cause significant haemodynamic …

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