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Long QT Syndrome

Known as: long q t syndrome, Ventricular arrhythmia associated with long QT syndrome, long q-t syndrome 
A ventricular arrhythmia characterized by a long QT interval, and accompanied by syncopal episodes sometimes leading to sudden death due to… Expand
National Institutes of Health

Papers overview

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Review
2019
Review
2019
Since the comprehensive recommendations for the management of acute promyelocytic leukemia (APL) reported in 2009, several… Expand
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Review
2018
Review
2018
SCN5A gene encodes the pore-forming ion-conducting α-subunit of the cardiac sodium channel (Nav1.5), which is responsible for the… Expand
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Review
2017
Review
2017
  • G. Tse, B. Yan
  • Europace : European pacing, arrhythmias, and…
  • 2017
  • Corpus ID: 9801944
Sudden cardiac death, frequently due to ventricular arrhythmias, is a significant problem globally. Most affected individuals do… Expand
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Highly Cited
2011
Highly Cited
2011
The ability to generate patient-specific human induced pluripotent stem cells (iPSCs) offers a new paradigm for modelling human… Expand
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Highly Cited
1997
Highly Cited
1997
Ion-channel β-subunits are ancillary proteins that co-assemble with α-subunits to modulate the gating kinetics and enhance… Expand
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Highly Cited
1995
Highly Cited
1995
To identify genes involved in cardiac arrhythmia, we investigated patients with long QT syndrome (LQT), an inherited disorder… Expand
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Highly Cited
1995
Highly Cited
1995
Long QT syndrome (LQT) is an inherited disorder that causes sudden death from cardiac arrhythmias, specifically torsade de… Expand
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Highly Cited
1995
Highly Cited
1995
BACKGROUND The long QT syndrome is an inherited disorder with prolonged ventricular repolarization and a propensity to… Expand
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Review
1993
Review
1993
T he idiopathic long QT syndrome (LQTS) is a congenital disease with frequent familial transmission, characterized primarily by… Expand
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Highly Cited
1991
Highly Cited
1991
BackgroundThe Long QT Syndrome (LQTS) is an infrequently occurring familial disorder in which affected individuals have… Expand
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