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Heart Rhythm|October 29, 2005
Drug-induced torsades de pointes: the evolving role of pharmacogeneticsPatrick T Fitzgerald, Michael J AckermanCurrent Opinion in Cardiology|November 7, 2012
Genetic testing in heritable cardiac arrhythmia syndromes: differentiating pathogenic mutations from background genetic noiseJohn R Giudicessi, Michael J AckermanEuropace : European Pacing, Arrhythmias, and Cardiac Electrophysiology : Journal of the Working Groups on Cardiac Pacing, Arrhythmias, and Cardiac Cellular Electrophysiology of the European Society of Cardiology|October 18, 2025
Implantable cardioverter defibrillators for long QT syndrome and catecholaminergic polymorphic ventricular tachycardia? (Not so fast, Louis)Peter J Schwartz, Michael J AckermanCardiovascular Research|May 26, 2005
Sudden infant death syndrome: how significant are the cardiac channelopathies?David J Tester, Michael J AckermanCirculation. Cardiovascular Genetics|February 9, 2013
Prevalence and potential genetic determinants of sensorineural deafness in KCNQ1 homozygosity and compound heterozygosityJohn R Giudicessi, Michael J AckermanInternational Journal of Cardiology|June 10, 2018
Role of genetic heart disease in sentinel sudden cardiac arrest survivors across the age spectrumJohn R Giudicessi, Michael J AckermanHeart Rhythm|December 17, 2008
Ventricular ectopy during treadmill exercise stress testing in the evaluation of long QT syndromeJustin M Horner, Michael J AckermanCirculation Research|August 21, 2010
Defining a new paradigm for human arrhythmia syndromes: phenotypic manifestations of gene mutations in ion channel- and transporter-associated proteinsMichael J Ackerman, Peter J MohlerAnnual Review of Medicine|October 22, 2008
Cardiomyopathic and channelopathic causes of sudden unexplained death in infants and childrenDavid J Tester, Michael J AckermanNature Reviews. Cardiology|February 1, 2012
Potassium-channel mutations and cardiac arrhythmias--diagnosis and therapyJohn R Giudicessi, Michael J AckermanPageof 73