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Eric Schulze

Showing results (81-90 of 155) with videos related to

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European Heart Journal|November 26, 2008
Transcriptional profiling of ion channel genes in Brugada syndrome and other right ventricular arrhythmogenic diseasesNathalie Gaborit, Thomas Wichter, Andras Varro, et al.
Plos One|July 11, 2013
A heterozygous deletion mutation in the cardiac sodium channel gene SCN5A with loss- and gain-of-function characteristics manifests as isolated conduction disease, without signs of Brugada or long QT syndromeSven Zumhagen, Marieke W Veldkamp, Birgit Stallmeyer, et al.
Europace : European Pacing, Arrhythmias, and Cardiac Electrophysiology : Journal of the Working Groups on Cardiac Pacing, Arrhythmias, and Cardiac Cellular Electrophysiology of the European Society of Cardiology|February 5, 2011
Successful treatment of catecholaminergic polymorphic ventricular tachycardia with flecainide: a case report and review of the current literatureChristian Pott, Dirk G Dechering, Florian Reinke, et al.
Journal of Molecular and Cellular Cardiology|March 23, 2010
The human CASQ2 mutation K206N is associated with hyperglycosylation and altered cellular calcium handlingUwe Kirchhefer, Diana Wehrmeister, Alex V Postma, et al.
International Journal of Cardiology|December 29, 2020
Functional characterization of novel alpha-helical rod domain desmin (DES) pathogenic variants associated with dilated cardiomyopathy, atrioventricular block and a risk for sudden cardiac deathBjörn Fischer, Sven Dittmann, Andreas Brodehl, et al.
Basic Research in Cardiology|May 7, 2013
Non dominant-negative KCNJ2 gene mutations leading to Andersen-Tawil syndrome with an isolated cardiac phenotypeMaren M Limberg, Sven Zumhagen, Michael F Netter, et al.
International Journal of Molecular Sciences|November 26, 2022
Whole Exome Sequencing Identifies a Heterozygous Variant in the Cav1.3 Gene <i>CACNA1D</i> Associated with Familial Sinus Node Dysfunction and Focal Idiopathic EpilepsySusanne Rinné, Birgit Stallmeyer, Alexandra Pinggera, et al.
Human Mutation|September 3, 2011
Mutational spectrum in the Ca(2+)--activated cation channel gene TRPM4 in patients with cardiac conductance disturbancesBirgit Stallmeyer, Sven Zumhagen, Isabelle Denjoy, et al.
Circulation|November 3, 2004
Abnormal myocardial presynaptic norepinephrine recycling in patients with Brugada syndromePeter Kies, Thomas Wichter, Michael Schäfers, et al.
Circulation Journal : Official Journal of the Japanese Circulation Society|June 30, 2015
A Common Mutation of Long QT Syndrome Type 1 in JapanHideki Itoh, Kenichi Dochi, Wataru Shimizu, et al.
Pageof 16

Showing results (81-90 of 155) with videos related to

Sort By:
Pageof 16
European Heart Journal|November 26, 2008
Transcriptional profiling of ion channel genes in Brugada syndrome and other right ventricular arrhythmogenic diseasesNathalie Gaborit, Thomas Wichter, Andras Varro, et al.
Plos One|July 11, 2013
A heterozygous deletion mutation in the cardiac sodium channel gene SCN5A with loss- and gain-of-function characteristics manifests as isolated conduction disease, without signs of Brugada or long QT syndromeSven Zumhagen, Marieke W Veldkamp, Birgit Stallmeyer, et al.
Europace : European Pacing, Arrhythmias, and Cardiac Electrophysiology : Journal of the Working Groups on Cardiac Pacing, Arrhythmias, and Cardiac Cellular Electrophysiology of the European Society of Cardiology|February 5, 2011
Successful treatment of catecholaminergic polymorphic ventricular tachycardia with flecainide: a case report and review of the current literatureChristian Pott, Dirk G Dechering, Florian Reinke, et al.
Journal of Molecular and Cellular Cardiology|March 23, 2010
The human CASQ2 mutation K206N is associated with hyperglycosylation and altered cellular calcium handlingUwe Kirchhefer, Diana Wehrmeister, Alex V Postma, et al.
International Journal of Cardiology|December 29, 2020
Functional characterization of novel alpha-helical rod domain desmin (DES) pathogenic variants associated with dilated cardiomyopathy, atrioventricular block and a risk for sudden cardiac deathBjörn Fischer, Sven Dittmann, Andreas Brodehl, et al.
Basic Research in Cardiology|May 7, 2013
Non dominant-negative KCNJ2 gene mutations leading to Andersen-Tawil syndrome with an isolated cardiac phenotypeMaren M Limberg, Sven Zumhagen, Michael F Netter, et al.
International Journal of Molecular Sciences|November 26, 2022
Whole Exome Sequencing Identifies a Heterozygous Variant in the Cav1.3 Gene <i>CACNA1D</i> Associated with Familial Sinus Node Dysfunction and Focal Idiopathic EpilepsySusanne Rinné, Birgit Stallmeyer, Alexandra Pinggera, et al.
Human Mutation|September 3, 2011
Mutational spectrum in the Ca(2+)--activated cation channel gene TRPM4 in patients with cardiac conductance disturbancesBirgit Stallmeyer, Sven Zumhagen, Isabelle Denjoy, et al.
Circulation|November 3, 2004
Abnormal myocardial presynaptic norepinephrine recycling in patients with Brugada syndromePeter Kies, Thomas Wichter, Michael Schäfers, et al.
Circulation Journal : Official Journal of the Japanese Circulation Society|June 30, 2015
A Common Mutation of Long QT Syndrome Type 1 in JapanHideki Itoh, Kenichi Dochi, Wataru Shimizu, et al.
Pageof 16