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Alfred L George

Showing results (241-250 of 270) with videos related to

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JAMA|April 11, 2013
Long QT syndrome-associated mutations in intrauterine fetal deathLia Crotti, David J Tester, Wendy M White, et al.
Circulation. Cardiovascular Genetics|July 17, 2013
Identification of a KCNQ1 polymorphism acting as a protective modifier against arrhythmic risk in long-QT syndromeSabine Duchatelet, Lia Crotti, Rachel A Peat, et al.
Circulation|February 8, 2013
Calmodulin mutations associated with recurrent cardiac arrest in infantsLia Crotti, Christopher N Johnson, Elisabeth Graf, et al.
Neurology. Genetics|March 16, 2017
Research conference summary from the 2014 International Task Force on <i>ATP1A3</i>-Related DisordersHendrik Rosewich, Matthew T Sweney, Suzanne DeBrosse, et al.
Nature Genetics|October 9, 2002
The K-Cl cotransporter KCC3 is mutant in a severe peripheral neuropathy associated with agenesis of the corpus callosumHeidi C Howard, David B Mount, Daniel Rochefort, et al.
Journal of the American College of Cardiology|December 3, 2013
Coxsackie and adenovirus receptor is a modifier of cardiac conduction and arrhythmia vulnerability in the setting of myocardial ischemiaRoos F J Marsman, Connie R Bezzina, Fabian Freiberg, et al.
Circulation. Arrhythmia and Electrophysiology|November 1, 2021
Understanding Circadian Mechanisms of Sudden Cardiac Death: A Report From the National Heart, Lung, and Blood Institute Workshop, Part 1: Basic and Translational AspectsBrian P Delisle, Alfred L George, Jeanne M Nerbonne, et al.
Circulation. Arrhythmia and Electrophysiology|November 1, 2021
Understanding Circadian Mechanisms of Sudden Cardiac Death: A Report From the National Heart, Lung, and Blood Institute Workshop, Part 2: Population and Clinical ConsiderationsBrian P Delisle, Alfred L George, Jeanne M Nerbonne, et al.
Medrxiv : the Preprint Server for Health Sciences|April 10, 2023
The impact of damaging epilepsy and cardiac genetic variant burden in sudden death in the youngMegan J Puckelwartz, Lorenzo L Pesce, Edgar J Hernandez, et al.
Elife|January 6, 2025
Plural molecular and cellular mechanisms of pore domain <i>KCNQ2</i> encephalopathyTimothy J Abreo, Emma C Thompson, Anuraag Madabushi, et al.
Pageof 27

Showing results (241-250 of 270) with videos related to

Sort By:
Pageof 27
JAMA|April 11, 2013
Long QT syndrome-associated mutations in intrauterine fetal deathLia Crotti, David J Tester, Wendy M White, et al.
Circulation. Cardiovascular Genetics|July 17, 2013
Identification of a KCNQ1 polymorphism acting as a protective modifier against arrhythmic risk in long-QT syndromeSabine Duchatelet, Lia Crotti, Rachel A Peat, et al.
Circulation|February 8, 2013
Calmodulin mutations associated with recurrent cardiac arrest in infantsLia Crotti, Christopher N Johnson, Elisabeth Graf, et al.
Neurology. Genetics|March 16, 2017
Research conference summary from the 2014 International Task Force on <i>ATP1A3</i>-Related DisordersHendrik Rosewich, Matthew T Sweney, Suzanne DeBrosse, et al.
Nature Genetics|October 9, 2002
The K-Cl cotransporter KCC3 is mutant in a severe peripheral neuropathy associated with agenesis of the corpus callosumHeidi C Howard, David B Mount, Daniel Rochefort, et al.
Journal of the American College of Cardiology|December 3, 2013
Coxsackie and adenovirus receptor is a modifier of cardiac conduction and arrhythmia vulnerability in the setting of myocardial ischemiaRoos F J Marsman, Connie R Bezzina, Fabian Freiberg, et al.
Circulation. Arrhythmia and Electrophysiology|November 1, 2021
Understanding Circadian Mechanisms of Sudden Cardiac Death: A Report From the National Heart, Lung, and Blood Institute Workshop, Part 1: Basic and Translational AspectsBrian P Delisle, Alfred L George, Jeanne M Nerbonne, et al.
Circulation. Arrhythmia and Electrophysiology|November 1, 2021
Understanding Circadian Mechanisms of Sudden Cardiac Death: A Report From the National Heart, Lung, and Blood Institute Workshop, Part 2: Population and Clinical ConsiderationsBrian P Delisle, Alfred L George, Jeanne M Nerbonne, et al.
Medrxiv : the Preprint Server for Health Sciences|April 10, 2023
The impact of damaging epilepsy and cardiac genetic variant burden in sudden death in the youngMegan J Puckelwartz, Lorenzo L Pesce, Edgar J Hernandez, et al.
Elife|January 6, 2025
Plural molecular and cellular mechanisms of pore domain <i>KCNQ2</i> encephalopathyTimothy J Abreo, Emma C Thompson, Anuraag Madabushi, et al.
Pageof 27