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Showing results (261-270 of 382) with videos related to

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Circulation. Cardiovascular Genetics|September 12, 2013
The role of CAV3 in long-QT syndrome: clinical and functional assessment of a caveolin-3/Kv11.1 double heterozygote versus caveolin-3 single heterozygotePaula L Hedley, Jørgen K Kanters, Maja Dembic, et al.
Heart (British Cardiac Society)|September 29, 2016
Comparison of hypertrophic cardiomyopathy in Afro-Caribbean versus white patients in the UKNabeel Sheikh, Michael Papadakis, Vasileios F Panoulas, et al.
International Journal of Cardiology|February 29, 2016
Whole exome sequence analysis reveals a homozygous mutation in PNPLA2 as the cause of severe dilated cardiomyopathy secondary to neutral lipid storage diseaseM Muggenthaler, E Petropoulou, S Omer, et al.
International Journal of Cardiology|May 21, 2019
Risk score for the exclusion of arrhythmic events in arrhythmogenic right ventricular cardiomyopathy at first presentationAnnina S Vischer, Silvia Castelletti, Petros Syrris, et al.
Circulation|May 20, 2024
Type 1 Brugada Pattern May Be Provoked by Ajmaline in Some Healthy Subjects: Results From a Clinical TrialBode Ensam, Chiara Scrocco, David Johnson, et al.
Circulation. Genomic and Precision Medicine|November 16, 2020
Prevalence and Phenotypic Correlations of Calmodulinopathy-Causative <i>CALM1-3</i> Variants Detected in a Multicenter Molecular Autopsy Cohort of Sudden Unexplained Death VictimsDaniel J Clemens, Belinda Gray, Richard D Bagnall, et al.
Circulation. Arrhythmia and Electrophysiology|November 28, 2022
The Utility of Sodium Channel Provocation in Unexplained Cardiac Arrest Survivors and Electrocardiographic Predictors of Ventricular Fibrillation RecurrenceBode Ensam, Christopher C Cheung, Fahad Almehmadi, et al.
Circulation. Arrhythmia and Electrophysiology|March 8, 2014
Burden of sudden cardiac death in persons aged 1 to 49 years: nationwide study in DenmarkBjarke Risgaard, Bo Gregers Winkel, Reza Jabbari, et al.
European Journal of Human Genetics : EJHG|February 4, 2018
Next-generation sequencing of AV nodal reentrant tachycardia patients identifies broad spectrum of variants in ion channel genesLaura Andreasen, Gustav Ahlberg, Chuyi Tang, et al.
Journal of Cardiovascular Electrophysiology|January 29, 2013
A KCNQ1 mutation causes a high penetrance for familial atrial fibrillationDaniel C Bartos, Jeffrey B Anderson, Rachel Bastiaenen, et al.
Pageof 39

Showing results (261-270 of 382) with videos related to

Sort By:
Pageof 39
Circulation. Cardiovascular Genetics|September 12, 2013
The role of CAV3 in long-QT syndrome: clinical and functional assessment of a caveolin-3/Kv11.1 double heterozygote versus caveolin-3 single heterozygotePaula L Hedley, Jørgen K Kanters, Maja Dembic, et al.
Heart (British Cardiac Society)|September 29, 2016
Comparison of hypertrophic cardiomyopathy in Afro-Caribbean versus white patients in the UKNabeel Sheikh, Michael Papadakis, Vasileios F Panoulas, et al.
International Journal of Cardiology|February 29, 2016
Whole exome sequence analysis reveals a homozygous mutation in PNPLA2 as the cause of severe dilated cardiomyopathy secondary to neutral lipid storage diseaseM Muggenthaler, E Petropoulou, S Omer, et al.
International Journal of Cardiology|May 21, 2019
Risk score for the exclusion of arrhythmic events in arrhythmogenic right ventricular cardiomyopathy at first presentationAnnina S Vischer, Silvia Castelletti, Petros Syrris, et al.
Circulation|May 20, 2024
Type 1 Brugada Pattern May Be Provoked by Ajmaline in Some Healthy Subjects: Results From a Clinical TrialBode Ensam, Chiara Scrocco, David Johnson, et al.
Circulation. Genomic and Precision Medicine|November 16, 2020
Prevalence and Phenotypic Correlations of Calmodulinopathy-Causative <i>CALM1-3</i> Variants Detected in a Multicenter Molecular Autopsy Cohort of Sudden Unexplained Death VictimsDaniel J Clemens, Belinda Gray, Richard D Bagnall, et al.
Circulation. Arrhythmia and Electrophysiology|November 28, 2022
The Utility of Sodium Channel Provocation in Unexplained Cardiac Arrest Survivors and Electrocardiographic Predictors of Ventricular Fibrillation RecurrenceBode Ensam, Christopher C Cheung, Fahad Almehmadi, et al.
Circulation. Arrhythmia and Electrophysiology|March 8, 2014
Burden of sudden cardiac death in persons aged 1 to 49 years: nationwide study in DenmarkBjarke Risgaard, Bo Gregers Winkel, Reza Jabbari, et al.
European Journal of Human Genetics : EJHG|February 4, 2018
Next-generation sequencing of AV nodal reentrant tachycardia patients identifies broad spectrum of variants in ion channel genesLaura Andreasen, Gustav Ahlberg, Chuyi Tang, et al.
Journal of Cardiovascular Electrophysiology|January 29, 2013
A KCNQ1 mutation causes a high penetrance for familial atrial fibrillationDaniel C Bartos, Jeffrey B Anderson, Rachel Bastiaenen, et al.
Pageof 39