Results 151 to 160 of about 20,149 (199)
Action potential clamp characterization of the S631A hERG mutation associated with short QT syndrome. [PDF]
Physiol Rep, 2018 Butler A +4 more
europepmc +1 more source
In silico Assessment of Pharmacotherapy for Human Atrial Patho-Electrophysiology Associated With hERG-Linked Short QT Syndrome. [PDF]
Front Physiol, 2018 Whittaker DG, Hancox JC, Zhang H.
europepmc +1 more source
Successful radiofrequency catheter ablation of a premature ventricular contraction triggering ventricular fibrillation in a patient with short QT syndrome. [PDF]
HeartRhythm Case Rep, 2019 Morimoto Y +5 more
europepmc +1 more source
Journal of the American College of Cardiology, 2011 Abnormalities in myocyte repolarization have been implicated for more than a half century in syndromes of unstable atrial and ventricular rhythms. Among the most well described and common of these abnormalities are those associated with the long QT syndrome (LQTS).
Jason D Roberts, Michael Gollob
exaly +4 more sources
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Cardiology in Review, 2009
Short QT syndrome is a new genetic disorder associated with familial atrial fibrillation and/or sudden death or syncope. To date, different mutations in genes encoding for cardiac ion channels (KCNH2, KCNQ1, and KCNJ2) have been identified to cause the short QT syndrome.
Christian, Wolpert +3 more
openaire +4 more sources
Short QT syndrome is a new genetic disorder associated with familial atrial fibrillation and/or sudden death or syncope. To date, different mutations in genes encoding for cardiac ion channels (KCNH2, KCNQ1, and KCNJ2) have been identified to cause the short QT syndrome.
Christian, Wolpert +3 more
openaire +4 more sources
Long QT Syndrome and Short QT Syndrome
Progress in Cardiovascular Diseases, 2008The long QT syndrome (LQTS) is a genetic disorder characterized by prolongation of the QT interval in the electrocardiogram (ECG) and a propensity to torsades de pointes ventricular tachycardia frequently leading to syncope, cardiac arrest, or sudden death usually in young otherwise healthy individuals.
Wojciech, Zareba, Iwona, Cygankiewicz
openaire +3 more sources
Herzschrittmachertherapie + Elektrophysiologie, 2012
Short QT syndrome was first described in 2000. It is a sporadic or familial ion channel disease that is associated with abbreviation of the QT interval permanently or transiently. The time of first manifestation of symptoms such as atrial fibrillation or syncope or even sudden death is between the 2nd and 4th decade.
C, Wolpert +7 more
openaire +2 more sources
Short QT syndrome was first described in 2000. It is a sporadic or familial ion channel disease that is associated with abbreviation of the QT interval permanently or transiently. The time of first manifestation of symptoms such as atrial fibrillation or syncope or even sudden death is between the 2nd and 4th decade.
C, Wolpert +7 more
openaire +2 more sources