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David J Tester

Showing results (191-200 of 212) with videos related to

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JAMA Cardiology|January 9, 2020
Identification of a Novel Homozygous Multi-Exon Duplication in RYR2 Among Children With Exertion-Related Unexplained Sudden Deaths in the Amish CommunityDavid J Tester, Hannah M Bombei, Kristi K Fitzgerald, et al.
Journal of the American Heart Association|November 24, 2021
Confirmation of Cause of Death Via Comprehensive Autopsy and Whole Exome Molecular Sequencing in People With Epilepsy and Sudden Unexpected DeathC Anwar A Chahal, David J Tester, Ahmed U Fayyaz, et al.
Circulation. Genomic and Precision Medicine|January 17, 2019
International Triadin Knockout Syndrome RegistryDaniel J Clemens, David J Tester, John R Giudicessi, et al.
Journal of the American College of Cardiology|November 21, 2009
Genotype-phenotype aspects of type 2 long QT syndromeWataru Shimizu, Arthur J Moss, Arthur A M Wilde, et al.
Journal of the American College of Cardiology|June 4, 2011
Distinguishing arrhythmogenic right ventricular cardiomyopathy/dysplasia-associated mutations from background genetic noiseJamie D Kapplinger, Andrew P Landstrom, Benjamin A Salisbury, et al.
JAMA|April 11, 2013
Long QT syndrome-associated mutations in intrauterine fetal deathLia Crotti, David J Tester, Wendy M White, et al.
American Journal of Physiology. Heart and Circulatory Physiology|March 21, 2020
Abnormal myocardial expression of SAP97 is associated with arrhythmogenic riskHassan Musa, Cherisse A Marcou, Todd J Herron, et al.
Lancet (London, England)|April 2, 2018
Dysfunction of NaV1.4, a skeletal muscle voltage-gated sodium channel, in sudden infant death syndrome: a case-control studyRoope Männikkö, Leonie Wong, David J Tester, et al.
Circulation|August 28, 2016
Clinical Aspects of Type 3 Long-QT Syndrome: An International Multicenter StudyArthur A M Wilde, Arthur J Moss, Elizabeth S Kaufman, et al.
Gastroenterology|March 12, 2014
Loss-of-function of the voltage-gated sodium channel NaV1.5 (channelopathies) in patients with irritable bowel syndromeArthur Beyder, Amelia Mazzone, Peter R Strege, et al.
Pageof 22

Showing results (191-200 of 212) with videos related to

Sort By:
Pageof 22
JAMA Cardiology|January 9, 2020
Identification of a Novel Homozygous Multi-Exon Duplication in RYR2 Among Children With Exertion-Related Unexplained Sudden Deaths in the Amish CommunityDavid J Tester, Hannah M Bombei, Kristi K Fitzgerald, et al.
Journal of the American Heart Association|November 24, 2021
Confirmation of Cause of Death Via Comprehensive Autopsy and Whole Exome Molecular Sequencing in People With Epilepsy and Sudden Unexpected DeathC Anwar A Chahal, David J Tester, Ahmed U Fayyaz, et al.
Circulation. Genomic and Precision Medicine|January 17, 2019
International Triadin Knockout Syndrome RegistryDaniel J Clemens, David J Tester, John R Giudicessi, et al.
Journal of the American College of Cardiology|November 21, 2009
Genotype-phenotype aspects of type 2 long QT syndromeWataru Shimizu, Arthur J Moss, Arthur A M Wilde, et al.
Journal of the American College of Cardiology|June 4, 2011
Distinguishing arrhythmogenic right ventricular cardiomyopathy/dysplasia-associated mutations from background genetic noiseJamie D Kapplinger, Andrew P Landstrom, Benjamin A Salisbury, et al.
JAMA|April 11, 2013
Long QT syndrome-associated mutations in intrauterine fetal deathLia Crotti, David J Tester, Wendy M White, et al.
American Journal of Physiology. Heart and Circulatory Physiology|March 21, 2020
Abnormal myocardial expression of SAP97 is associated with arrhythmogenic riskHassan Musa, Cherisse A Marcou, Todd J Herron, et al.
Lancet (London, England)|April 2, 2018
Dysfunction of NaV1.4, a skeletal muscle voltage-gated sodium channel, in sudden infant death syndrome: a case-control studyRoope Männikkö, Leonie Wong, David J Tester, et al.
Circulation|August 28, 2016
Clinical Aspects of Type 3 Long-QT Syndrome: An International Multicenter StudyArthur A M Wilde, Arthur J Moss, Elizabeth S Kaufman, et al.
Gastroenterology|March 12, 2014
Loss-of-function of the voltage-gated sodium channel NaV1.5 (channelopathies) in patients with irritable bowel syndromeArthur Beyder, Amelia Mazzone, Peter R Strege, et al.
Pageof 22