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pubmed-article:17916157pubmed:abstractTextThe QTc interval prolongation is not a perfect surrogate marker of the presence of an increased risk for arrhythmic events. In the search for alternative markers, we investigated the T-amplitude and QT interval adaptation to heart rate (HR) in patients with the congenital long QT syndrome (LQTS) and individuals with sotalol-induced QT prolongation.lld:pubmed
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pubmed-article:17916157pubmed:dateRevised2008-10-28lld:pubmed
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pubmed-article:17916157pubmed:articleTitleImpaired T-amplitude adaptation to heart rate characterizes I(Kr) inhibition in the congenital and acquired forms of the long QT syndrome.lld:pubmed
pubmed-article:17916157pubmed:affiliationHeart Research Follow-Up Program, Cardiology Department, University of Rochester Medical Center, Rochester, New York, USA. jean-philippe.couderc@heart.rochester.edulld:pubmed
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