Search research articles
Contact Us
Filters
Showing results (131-140 of 155) with videos related to
Page
of 16
Sort By:
Circulation. Genomic and Precision Medicine
|
August 21, 2019
Cardiac α-Actin (ACTC1) Gene Mutation Causes Atrial-Septal Defects Associated With Late-Onset Dilated Cardiomyopathy
Derk Frank, Ashraf Yusuf Rangrez, Corinna Friedrich, et al.
Journal of Molecular and Cellular Cardiology
|
June 15, 2020
POPDC2 a novel susceptibility gene for conduction disorders
Susanne Rinné, Beatriz Ortiz-Bonnin, Birgit Stallmeyer, et al.
Nature Genetics
|
October 19, 2004
Mutations in the desmosomal protein plakophilin-2 are common in arrhythmogenic right ventricular cardiomyopathy
Brenda Gerull, Arnd Heuser, Thomas Wichter, et al.
Heart Rhythm
|
February 22, 2023
Genetic analysis identifies the SLC4A3 anion exchanger as a major gene for short QT syndrome
Morten Krogh Christiansen, Kasper Kjær-Sørensen, Natacha C Clavsen, et al.
Circulation. Genomic and Precision Medicine
|
August 7, 2019
Arrhythmogenic Right Ventricular Cardiomyopathy-Associated Desmosomal Variants Are Rarely De Novo
Freyja H M van Lint, Brittney Murray, Crystal Tichnell, et al.
Circulation. Cardiovascular Genetics
|
March 5, 2015
Analysis for Genetic Modifiers of Disease Severity in Patients With Long-QT Syndrome Type 2
Iris C R M Kolder, Michael W T Tanck, Pieter G Postema, et al.
Heart Rhythm
|
December 15, 2024
Novel risk predictor of arrhythmias for patients with potassium channel-related congenital long QT syndrome
Christian Krijger Juárez, Virginnio M Proost, Michael W Tanck, et al.
Heart Rhythm
|
February 5, 2010
An international compendium of mutations in the SCN5A-encoded cardiac sodium channel in patients referred for Brugada syndrome genetic testing
Jamie D Kapplinger, David J Tester, Marielle Alders, et al.
Circulation. Genomic and Precision Medicine
|
February 10, 2021
Cadherin 2-Related Arrhythmogenic Cardiomyopathy: Prevalence and Clinical Features
Alice Ghidoni, Perry M Elliott, Petros Syrris, et al.
European Heart Journal. Quality of Care & Clinical Outcomes
|
July 11, 2025
Current Management of Transition and Multidisciplinary Care of Patients with Inherited and Rare Cardiomyopathies in Europe: Results of the European Reference Network for Rare and Low Prevalence Complex Diseases of the Heart (ERN GUARD-HEART)
Emanuele Monda, Elena Biagini, Nico Blom, et al.
Page
of 16
Search research articles
Search
Showing results (131-140 of 155) with videos related to
Sort By:
Page
of 16
Circulation. Genomic and Precision Medicine
|
August 21, 2019
Cardiac α-Actin (ACTC1) Gene Mutation Causes Atrial-Septal Defects Associated With Late-Onset Dilated Cardiomyopathy
Derk Frank, Ashraf Yusuf Rangrez, Corinna Friedrich, et al.
Journal of Molecular and Cellular Cardiology
|
June 15, 2020
POPDC2 a novel susceptibility gene for conduction disorders
Susanne Rinné, Beatriz Ortiz-Bonnin, Birgit Stallmeyer, et al.
Nature Genetics
|
October 19, 2004
Mutations in the desmosomal protein plakophilin-2 are common in arrhythmogenic right ventricular cardiomyopathy
Brenda Gerull, Arnd Heuser, Thomas Wichter, et al.
Heart Rhythm
|
February 22, 2023
Genetic analysis identifies the SLC4A3 anion exchanger as a major gene for short QT syndrome
Morten Krogh Christiansen, Kasper Kjær-Sørensen, Natacha C Clavsen, et al.
Circulation. Genomic and Precision Medicine
|
August 7, 2019
Arrhythmogenic Right Ventricular Cardiomyopathy-Associated Desmosomal Variants Are Rarely De Novo
Freyja H M van Lint, Brittney Murray, Crystal Tichnell, et al.
Circulation. Cardiovascular Genetics
|
March 5, 2015
Analysis for Genetic Modifiers of Disease Severity in Patients With Long-QT Syndrome Type 2
Iris C R M Kolder, Michael W T Tanck, Pieter G Postema, et al.
Heart Rhythm
|
December 15, 2024
Novel risk predictor of arrhythmias for patients with potassium channel-related congenital long QT syndrome
Christian Krijger Juárez, Virginnio M Proost, Michael W Tanck, et al.
Heart Rhythm
|
February 5, 2010
An international compendium of mutations in the SCN5A-encoded cardiac sodium channel in patients referred for Brugada syndrome genetic testing
Jamie D Kapplinger, David J Tester, Marielle Alders, et al.
Circulation. Genomic and Precision Medicine
|
February 10, 2021
Cadherin 2-Related Arrhythmogenic Cardiomyopathy: Prevalence and Clinical Features
Alice Ghidoni, Perry M Elliott, Petros Syrris, et al.
European Heart Journal. Quality of Care & Clinical Outcomes
|
July 11, 2025
Current Management of Transition and Multidisciplinary Care of Patients with Inherited and Rare Cardiomyopathies in Europe: Results of the European Reference Network for Rare and Low Prevalence Complex Diseases of the Heart (ERN GUARD-HEART)
Emanuele Monda, Elena Biagini, Nico Blom, et al.
Page
of 16