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Paroxysmal familial ventricular fibrillation

Known as: Idiopathic ventricular fibrillation, Paroxysmal ventricular fibrillation, VENTRICULAR FIBRILLATION, PAROXYSMAL FAMILIAL 
 
National Institutes of Health

Papers overview

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Highly Cited
2010
Highly Cited
2010
BACKGROUND L-type calcium channel (LTCC) mutations have been associated with Brugada syndrome (BrS), short QT (SQT) syndrome, and… Expand
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Highly Cited
2009
Highly Cited
2009
Background: Early repolarization in the inferolateral leads has been recently recognized as a frequent syndrome associated with… Expand
Highly Cited
2007
Highly Cited
2007
Background— Brugada syndrome is a rare, autosomal-dominant, male-predominant form of idiopathic ventricular fibrillation… Expand
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Highly Cited
2006
Highly Cited
2006
Objectives: We performed a meta‐analysis of prognostic studies of patients with a Brugada ECG to assess predictors of events. 
Highly Cited
2004
Highly Cited
2004
Background—The electrocardiographic short QT-interval syndrome forms a distinct clinical entity presenting with a high rate of… Expand
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Highly Cited
2002
Highly Cited
2002
Background—Mutations in the cardiac ryanodine receptor gene (RyR2) underlie catecholaminergic polymorphic ventricular tachycardia… Expand
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Highly Cited
2002
Highly Cited
2002
Background—Brugada syndrome is a form of idiopathic ventricular fibrillation characterized by a right bundle-branch block pattern… Expand
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Highly Cited
1998
Highly Cited
1998
Ventricular fibrillation causes more than 300, 000 sudden deaths each year in the USA alone,. In approximately 5–12% of these… Expand
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Review
1997
Review
1997
BACKGROUND A wide variety of structural abnormalities are associated with the vast majority of cardiac arrests. However, there is… Expand
Highly Cited
1989
Highly Cited
1989
Since 1977, six patients (five males and one female), aged 14 to 35 years, resuscitated from ventricular fibrillation, were… Expand
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