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J Ackerman

Showing results (1021-1030 of 1,140) 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.
Heart Rhythm|February 2, 2013
Prognostic implications of mutation-specific QTc standard deviation in congenital long QT syndromeAndrew Mathias, Arthur J Moss, Coeli M Lopes, et al.
ACS Central Science|June 3, 2021
Chemical Inhibition of ENL/AF9 YEATS Domains in Acute LeukemiaLeopold Garnar-Wortzel, Timothy R Bishop, Seiya Kitamura, et al.
Journal of the American College of Cardiology|February 22, 2020
Detection of Hypertrophic Cardiomyopathy Using a Convolutional Neural Network-Enabled ElectrocardiogramWei-Yin Ko, Konstantinos C Siontis, Zachi I Attia, et al.
Heart Rhythm|July 17, 2018
Supraventricular tachycardias, conduction disease, and cardiomyopathy in 3 families with the same rare variant in TNNI3K (p.Glu768Lys)Svitlana Podliesna, Julian Delanne, Lindsey Miller, et al.
Heart Rhythm|March 29, 2011
Mutation and gender-specific risk in type 2 long QT syndrome: implications for risk stratification for life-threatening cardiac events in patients with long QT syndromeDimitry Migdalovich, Arthur J Moss, Coeli M Lopes, et al.
Heart Rhythm|February 2, 2012
Combined assessment of sex- and mutation-specific information for risk stratification in type 1 long QT syndromeJason Costa, Coeli M Lopes, Alon Barsheshet, et al.
European Heart Journal|September 22, 2018
An autoantibody identifies arrhythmogenic right ventricular cardiomyopathy and participates in its pathogenesisDiptendu Chatterjee, Meena Fatah, Deniz Akdis, et al.
The Journal of Clinical Endocrinology and Metabolism|January 30, 2014
The influence of rare genetic variation in SLC30A8 on diabetes incidence and β-cell functionLiana K Billings, Kathleen A Jablonski, Rachel J Ackerman, et al.
Journal of the American College of Cardiology|February 19, 2011
Risk factors for recurrent syncope and subsequent fatal or near-fatal events in children and adolescents with long QT syndromeJudy F Liu, Christian Jons, Arthur J Moss, et al.
Pageof 114

Showing results (1021-1030 of 1,140) with videos related to

Sort By:
Pageof 114
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.
Heart Rhythm|February 2, 2013
Prognostic implications of mutation-specific QTc standard deviation in congenital long QT syndromeAndrew Mathias, Arthur J Moss, Coeli M Lopes, et al.
ACS Central Science|June 3, 2021
Chemical Inhibition of ENL/AF9 YEATS Domains in Acute LeukemiaLeopold Garnar-Wortzel, Timothy R Bishop, Seiya Kitamura, et al.
Journal of the American College of Cardiology|February 22, 2020
Detection of Hypertrophic Cardiomyopathy Using a Convolutional Neural Network-Enabled ElectrocardiogramWei-Yin Ko, Konstantinos C Siontis, Zachi I Attia, et al.
Heart Rhythm|July 17, 2018
Supraventricular tachycardias, conduction disease, and cardiomyopathy in 3 families with the same rare variant in TNNI3K (p.Glu768Lys)Svitlana Podliesna, Julian Delanne, Lindsey Miller, et al.
Heart Rhythm|March 29, 2011
Mutation and gender-specific risk in type 2 long QT syndrome: implications for risk stratification for life-threatening cardiac events in patients with long QT syndromeDimitry Migdalovich, Arthur J Moss, Coeli M Lopes, et al.
Heart Rhythm|February 2, 2012
Combined assessment of sex- and mutation-specific information for risk stratification in type 1 long QT syndromeJason Costa, Coeli M Lopes, Alon Barsheshet, et al.
European Heart Journal|September 22, 2018
An autoantibody identifies arrhythmogenic right ventricular cardiomyopathy and participates in its pathogenesisDiptendu Chatterjee, Meena Fatah, Deniz Akdis, et al.
The Journal of Clinical Endocrinology and Metabolism|January 30, 2014
The influence of rare genetic variation in SLC30A8 on diabetes incidence and β-cell functionLiana K Billings, Kathleen A Jablonski, Rachel J Ackerman, et al.
Journal of the American College of Cardiology|February 19, 2011
Risk factors for recurrent syncope and subsequent fatal or near-fatal events in children and adolescents with long QT syndromeJudy F Liu, Christian Jons, Arthur J Moss, et al.
Pageof 114