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Clinics in Sports Medicine|June 24, 2015
Athletes with Implantable Cardioverter DefibrillatorsShiva P Ponamgi, Christopher V DeSimone, Michael J Ackerman
Journal of the American Society of Echocardiography : Official Publication of the American Society of Echocardiography|June 5, 2003
Diastolic ventricular dysfunction as a marker for hypertrophic cardiomyopathy in a family with a novel alpha-tropomyosin mutationMichael G Earing, Michael J Ackerman, Patrick W O'Leary
Revista Espanola De Cardiologia (English Ed.)|April 30, 2014
Personalized medicine: genetic diagnosis for inherited cardiomyopathies/channelopathiesMichael J Ackerman, Cherisse A Marcou, David J Tester
Pacing and Clinical Electrophysiology : PACE|April 22, 2011
Holter monitoring in the evaluation of congenital long QT syndromeDaniel A Mauriello, Jonathan N Johnson, Michael J Ackerman
Current Opinion in Cardiology|April 7, 2007
Genetics of hypertrophic cardiomyopathy: one, two, or more diseases?J Martijn Bos, Steve R Ommen, Michael J Ackerman
Methods in Molecular Medicine|October 31, 2006
Mutation detection in congenital long QT syndrome: cardiac channel gene screen using PCR, dHPLC, and direct DNA sequencingDavid J Tester, Melissa L Will, Michael J Ackerman
Cardiology in the Young|March 27, 2014
Marked, transient, emotion-triggered QT accentuation in an adolescent female with type 1 long QT syndromeHeather N Anderson, Beth A Medford, Michael J Ackerman
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