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JAMA
|
April 11, 2013
Long QT syndrome-associated mutations in intrauterine fetal death
Lia 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 syndrome
Sabine Duchatelet, Lia Crotti, Rachel A Peat, et al.
Circulation
|
February 8, 2013
Calmodulin mutations associated with recurrent cardiac arrest in infants
Lia 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 Disorders
Hendrik 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 callosum
Heidi 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 ischemia
Roos 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 Aspects
Brian 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 Considerations
Brian 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 young
Megan 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> encephalopathy
Timothy J Abreo, Emma C Thompson, Anuraag Madabushi, et al.
Page
of 27
Search research articles
Search
Showing results (241-250 of 270) with videos related to
Sort By:
Page
of 27
JAMA
|
April 11, 2013
Long QT syndrome-associated mutations in intrauterine fetal death
Lia 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 syndrome
Sabine Duchatelet, Lia Crotti, Rachel A Peat, et al.
Circulation
|
February 8, 2013
Calmodulin mutations associated with recurrent cardiac arrest in infants
Lia 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 Disorders
Hendrik 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 callosum
Heidi 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 ischemia
Roos 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 Aspects
Brian 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 Considerations
Brian 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 young
Megan 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> encephalopathy
Timothy J Abreo, Emma C Thompson, Anuraag Madabushi, et al.
Page
of 27