Long QT syndrome type 3

 
National Institutes of Health

Topic mentions per year

Topic mentions per year

2003-2018
012320032018

Papers overview

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Review
2018
Review
2018
Congenital long QT syndrome type 3 (LQT3) is the third in frequency compared to the 15 forms known currently of congenital long… (More)
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2016
2016
BACKGROUND Long QT syndrome type 3 (LQT3) is a lethal disease caused by gain-of-function mutations in the SCN5A gene, coding for… (More)
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2012
2012
BACKGROUND Atrial fibrillation (AF) is the most common cardiac arrhythmia. The cardiac sodium channel, Na(V)1.5, plays a pivotal… (More)
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2010
2010
A female infant presented with bradycardia and an electrocardiogram demonstrating 2:1 atrioventricular depolarization, a… (More)
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2009
2009
Various entities and genetic etiologies, including inherited long QT syndrome type 3 (LQT3), contribute to sudden infant death… (More)
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2007
2007
The experiments investigated the applicability of two established criteria for arrhythmogenicity in Scn5a+/Δ and Scn5a+/− murine… (More)
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2006
2006
BACKGROUND The autonomic nervous system has been implicated in several arrhythmogenic diseases, including long QT syndrome type 3… (More)
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2005
2005
OBJECTIVES The aim was to investigate at what age electrocardiographic characteristics of long QT syndrome type 3 (LQT3) and… (More)
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2004
2004
INTRODUCTION Brugada syndrome is characterized by sudden death secondary to malignant arrhythmias and the presence of ST segment… (More)
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2003
2003
Congenital long QT syndrome type 3 (LQT3) is caused by mutations in the gene SCN5A encoding the alpha-subunit of the cardiac Na… (More)
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