Long QT syndromes and torsade de pointes
Author:
Publisher
Elsevier BV
Subject
General Medicine
Reference85 articles.
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3. Differential response to Na+ channel blockade, beta-adrenergic stimulation and rapid pacing in a cellular model mimicking the SCN5A and HERG defects present in the long QT syndrome: experimental basis for gene-specific therapy;Priori;Circ Res,1996
4. Improvement of repolarization abnormalities by a K+ channel opener in the LQT1 form of the congenital long-QT syndrome;Shimizu;Circulation,1998
5. Genetically defined therapy of inherited long QT syndrome: correction of abnormal repolarisation by potassium;Compton;Circulation,1996
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