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SHORT QT SYNDROME 2 (disorder)

Known as: SHORT QT SYNDROME 2, SQT2 
National Institutes of Health

Related topics

Related topics

5 relations
Autosomal dominant inheritanceKCNQ1 geneVentricular Fibrillation

Broader (2)

Cardiac conduction systemCongenital Heart Defects

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2017
2017
Modeling the effects of amiodarone on short QT syndrome variant 2 in the human ventricles.
AIMS The short QT syndrome (SQTS) is a new genetic disorder associated with atrial and ventricular arrhythmias and sudden death… 
2015
2015
In silico investigation of short QT syndrome-linked potassium channel mutations on electro-mechanical function of human atrial cells
Short QT syndrome (SQTS) patients are prone to atrial arrhythmias. However, the link between SQTS gene mutations and atrial pro… 
2015
2015
Closed-loop investigation of the dynamical properties of cardiomyocyte electrophysiology by means of Dynamic clamp and Mathematical modelling
The research field of my PhD concerns mathematical modeling and numerical simulation, applied to the cardiac electrophysiology… 
2013
2013
Is exercise-related QT interval shortening with a peaked T wave a specific electrocardiographic finding of pheochromocytoma?
Review
2011
Review
2011
Short QT Syndrome: Clinical Presentation, Molecular, Genetic, Cellular, and Ionic Basis
Short QT Syndrome is a recently recognized inherited channelopathy responsible for sudden cardiac death (SCD) in individuals with… 
2010
2010
Congenital Short QT Syndrome
The Short QT Syndrome is a recently described new genetic disorder, characterized by abnormally short QT interval, paroxysmal… 
2010
2010
POTENTIAL CLAMP AND MEFLOQUINE SENSITIVITY OF RECOMBINANT ' IKS ' CHANNELS INCORPORATING THE V 307 L KCNQ 1 MUTATION
A number of different potassium channels contribute to repolarisation of cardiac ventricular action potentials (1). The rapid and… 
2007
2007
The phenotype of a KCNQ1 mutation depends on its KCNE partners: is the cardiac slow delayed rectifier (IKs) channel more than a KCNQ1/KCNE1 complex?
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