Article
Romano-Ward and other congenital long QT syndromes.
Cardiovascular drugs and therapy - 1 Jan 2002
Bloise Raffaella, Napolitano Carlo, Priori Silvia G
Abstract excerpt
Molecular genetics applied to the study of inherited arrhythmogenic diseases has profoundly modified our understanding of cardiac electrophysiology providing new information on the crucial pathophysiological role of cardiac ion channels. These data are now putting forth innovative strategies for clinical management of the affected patients. Among these conditions, long QT syndrome (LQTS) was the first to enter...
Read the complete abstract on PubMedTopics
Share this publication in a Topic to start or enrich a Post.
