Background—The congenital long-QT syndrome (LQTS) is caused by mutations on several
genes, all of which encode cardiac ion channels. The progressive understanding of the …

Long QT syndrome (LQT) is an inherited disorder that causes sudden death from cardiac
arrhythmias, specifically torsade de pointes and ventricular fibrillation. We previously mapped …

Background—Long-QT Syndrome (LQTS) is a cardiovascular disorder characterized by
prolongation of the QT interval on ECG and presence of syncope, seizures, and sudden death. …

Diet modulates the gut microbiome, which in turn can impact the immune system. Here, we
determined how two microbiota-targeted dietary interventions, plant-based fiber and …

Background—β-blockers are routinely prescribed in congenital long-QT syndrome (LQTS),
but the effectiveness and limitations of β-blockers in this disorder have not been evaluated. …

Background The congenital long-QT syndrome, caused by mutations in cardiac potassium-channel
genes (KVLQT1 at the LQT1 locus and HERG at the LQT2 locus) and the sodium-…

Background— The management of long-QT syndrome (LQTS) patients who continue to have
cardiac events (CEs) despite β-blockers is complex. We assessed the long-term efficacy of …

BACKGROUND: Although structural neuroimaging methods have been widely used to study
brain morphology in schizophrenia, synthesizing this literature has been difficult. With the …

Background The long QT syndrome is an inherited disorder with prolonged ventricular
repolarization and a propensity to ventricular tachyarrhythmias and sudden arrhythmic death. …

Background—Congenital long-QT syndrome (LQTS) is caused by mutations of genes encoding
the slow component of the delayed rectifier current (LQT1, LQT5), the rapid component …