Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

David J Tester

Showing results (21-30 of 212) with videos related to

Pageof 22
Sort By:
Mayo Clinic Proceedings|October 4, 2011
Unexplained drownings and the cardiac channelopathies: a molecular autopsy seriesDavid J Tester, Argelia Medeiros-Domingo, Melissa L Will, et al.
Journal of Child Neurology|April 17, 2010
Cardiac channel molecular autopsy for sudden unexpected death in epilepsyJonathan N Johnson, David J Tester, Nancy E Bass, et al.
Heart Rhythm|September 29, 2005
Spectrum and prevalence of cardiac ryanodine receptor (RyR2) mutations in a cohort of unrelated patients referred explicitly for long QT syndrome genetic testingDavid J Tester, Laura J Kopplin, Melissa L Will, et al.
Journal of the American College of Cardiology|February 21, 2006
Effect of clinical phenotype on yield of long QT syndrome genetic testingDavid J Tester, Melissa L Will, Carla M Haglund, et al.
Circulation. Arrhythmia and Electrophysiology|October 22, 2009
Protein kinase A-dependent biophysical phenotype for V227F-KCNJ2 mutation in catecholaminergic polymorphic ventricular tachycardiaAmanda L Vega, David J Tester, Michael J Ackerman, et al.
Circulation. Cardiovascular Genetics|April 27, 2016
Whole-Exome Molecular Autopsy After Exertion-Related Sudden Unexplained Death in the YoungJason H Anderson, David J Tester, Melissa L Will, et al.
Heart Rhythm|April 21, 2005
Compendium of cardiac channel mutations in 541 consecutive unrelated patients referred for long QT syndrome genetic testingDavid J Tester, Melissa L Will, Carla M Haglund, et al.
Circulation|May 16, 2007
Diagnostic miscues in congenital long-QT syndromeNathaniel W Taggart, Carla M Haglund, David J Tester, et al.
Circulation. Genomic and Precision Medicine|November 16, 2020
Patients With Hypertrophic Cardiomyopathy Deemed Genotype Negative Based on Research Grade Genetic Analysis: Time for Repeat Diagnostic Testing With Next-Generation SequencingBailey J O'Hare, J Martijn Bos, David J Tester, et al.
Circulation|February 21, 2020
Variant Frequency and Clinical Phenotype Call Into Question the Nature of Minor, Nonsyndromic Long-QT Syndrome-Susceptibility Gene-Disease AssociationsJohn R Giudicessi, Ram K Rohatgi, David J Tester, et al.
Pageof 22

Showing results (21-30 of 212) with videos related to

Sort By:
Pageof 22
Mayo Clinic Proceedings|October 4, 2011
Unexplained drownings and the cardiac channelopathies: a molecular autopsy seriesDavid J Tester, Argelia Medeiros-Domingo, Melissa L Will, et al.
Journal of Child Neurology|April 17, 2010
Cardiac channel molecular autopsy for sudden unexpected death in epilepsyJonathan N Johnson, David J Tester, Nancy E Bass, et al.
Heart Rhythm|September 29, 2005
Spectrum and prevalence of cardiac ryanodine receptor (RyR2) mutations in a cohort of unrelated patients referred explicitly for long QT syndrome genetic testingDavid J Tester, Laura J Kopplin, Melissa L Will, et al.
Journal of the American College of Cardiology|February 21, 2006
Effect of clinical phenotype on yield of long QT syndrome genetic testingDavid J Tester, Melissa L Will, Carla M Haglund, et al.
Circulation. Arrhythmia and Electrophysiology|October 22, 2009
Protein kinase A-dependent biophysical phenotype for V227F-KCNJ2 mutation in catecholaminergic polymorphic ventricular tachycardiaAmanda L Vega, David J Tester, Michael J Ackerman, et al.
Circulation. Cardiovascular Genetics|April 27, 2016
Whole-Exome Molecular Autopsy After Exertion-Related Sudden Unexplained Death in the YoungJason H Anderson, David J Tester, Melissa L Will, et al.
Heart Rhythm|April 21, 2005
Compendium of cardiac channel mutations in 541 consecutive unrelated patients referred for long QT syndrome genetic testingDavid J Tester, Melissa L Will, Carla M Haglund, et al.
Circulation|May 16, 2007
Diagnostic miscues in congenital long-QT syndromeNathaniel W Taggart, Carla M Haglund, David J Tester, et al.
Circulation. Genomic and Precision Medicine|November 16, 2020
Patients With Hypertrophic Cardiomyopathy Deemed Genotype Negative Based on Research Grade Genetic Analysis: Time for Repeat Diagnostic Testing With Next-Generation SequencingBailey J O'Hare, J Martijn Bos, David J Tester, et al.
Circulation|February 21, 2020
Variant Frequency and Clinical Phenotype Call Into Question the Nature of Minor, Nonsyndromic Long-QT Syndrome-Susceptibility Gene-Disease AssociationsJohn R Giudicessi, Ram K Rohatgi, David J Tester, et al.
Pageof 22