Background: Mutations in the cardiac sodium channel, SCN5A, have been associated with one type of long-QT syndrome, with isolated cardiac conduction defects and Brugada syndrome. The sodium ...

International guidelines suggest that a significant majority of patients with Hypertrophic Cardiomopathy (HCM), Long QT syndrome (LQTS) and Catecholaminergic Polymorphic Centricular Tachycardiac (CPVT ...

Wang Q, Shen J, Splawski I, et al. SCN5A mutations associated with an inherited cardiac arrhythmia, long QT syndrome. Cell. 1995;80:805–811. Crossref. PubMed. Google Scholar. 74. Schott JJ, ...

Background and Purpose:This scientific statement provides an interprofessional, comprehensive review of evidence and recommendations for indications, duration, and implementation of continuous electro ...

Introduction. Cardiovascular diseases are the most common cause of loss of flying licence globally, and cardiac arrhythmia is the main disqualifier in a substantial proportion of aircrew.1 Frequent ...

The Scn5a+/- genotype caused an independent increase of VERP regardless of whether the recording site was the RVOT or RV. Effective AP conduction velocities (CV†s), derived from fitting regression ...

The impact of KCNQ1, hERG and SCN5A on acquired LQTS needs further research. There was a correlation between fenfluramine-induced pulmonary hypertension and mutations of BMPR2.

Instead of the six-class fQRS morphology of Das et al. (2006) and the ten-class morphology of Maheshwari et al. (2013) we have developed more detailed morphology classification of five classes and 15 ...