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Eric Schulze

Showing results (61-70 of 155) with videos related to

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Herzschrittmachertherapie & Elektrophysiologie|February 19, 2014
[Long QT-syndromes: diagnosis and genetics]Eric Schulze-Bahr, Gerold Mönnig, Dörte Etzrodt, et al.
European Journal of Nuclear Medicine and Molecular Imaging|June 22, 2011
Impaired cardiac sympathetic innervation in symptomatic patients with long QT syndromePeter Kies, Matthias Paul, Joachim Gerss, 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|October 3, 2012
T-wave integral: an electrocardiographic marker discriminating patients with arrhythmogenic right ventricular cardiomyopathy from patients with right ventricular outflow tract tachycardiaAlexander Samol, Christian Wollmann, Christian Vahlhaus, et al.
Journal of Cardiovascular Electrophysiology|October 3, 2003
Prolonged atrial action potential durations and polymorphic atrial tachyarrhythmias in patients with long QT syndromePaulus Kirchhof, Lars Eckardt, Michael R Franz, et al.
Journal of Cardiovascular Electrophysiology|September 6, 2002
Body surface area of ST elevation and the presence of late potentials correlate to the inducibility of ventricular tachyarrhythmias in Brugada syndromeLars Eckardt, Hans-Jürgen Bruns, Matthias Paul, et al.
European Journal of Nuclear Medicine and Molecular Imaging|November 25, 2011
Microvascular dysfunction in nonfailing arrhythmogenic right ventricular cardiomyopathyMatthias Paul, Kambiz Rahbar, Joachim Gerss, et al.
EMBO Molecular Medicine|June 29, 2014
Gain-of-function mutation in TASK-4 channels and severe cardiac conduction disorderCorinna Friedrich, Susanne Rinné, Sven Zumhagen, et al.
The Journal of Clinical Investigation|September 4, 2009
Impaired endocytosis of the ion channel TRPM4 is associated with human progressive familial heart block type IMartin Kruse, Eric Schulze-Bahr, Valerie Corfield, et al.
Cardiovascular Research|July 26, 2005
Substitution of a conserved alanine in the domain IIIS4-S5 linker of the cardiac sodium channel causes long QT syndromeJeroen P P Smits, Marieke W Veldkamp, Connie R Bezzina, et al.
Plos One|July 6, 2016
Improved Clinical Risk Stratification in Patients with Long QT Syndrome? Novel Insights from Multi-Channel ECGsAlexander Samol, Mehmet Gönes, Sven Zumhagen, et al.
Pageof 16

Showing results (61-70 of 155) with videos related to

Sort By:
Pageof 16
Herzschrittmachertherapie & Elektrophysiologie|February 19, 2014
[Long QT-syndromes: diagnosis and genetics]Eric Schulze-Bahr, Gerold Mönnig, Dörte Etzrodt, et al.
European Journal of Nuclear Medicine and Molecular Imaging|June 22, 2011
Impaired cardiac sympathetic innervation in symptomatic patients with long QT syndromePeter Kies, Matthias Paul, Joachim Gerss, 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|October 3, 2012
T-wave integral: an electrocardiographic marker discriminating patients with arrhythmogenic right ventricular cardiomyopathy from patients with right ventricular outflow tract tachycardiaAlexander Samol, Christian Wollmann, Christian Vahlhaus, et al.
Journal of Cardiovascular Electrophysiology|October 3, 2003
Prolonged atrial action potential durations and polymorphic atrial tachyarrhythmias in patients with long QT syndromePaulus Kirchhof, Lars Eckardt, Michael R Franz, et al.
Journal of Cardiovascular Electrophysiology|September 6, 2002
Body surface area of ST elevation and the presence of late potentials correlate to the inducibility of ventricular tachyarrhythmias in Brugada syndromeLars Eckardt, Hans-Jürgen Bruns, Matthias Paul, et al.
European Journal of Nuclear Medicine and Molecular Imaging|November 25, 2011
Microvascular dysfunction in nonfailing arrhythmogenic right ventricular cardiomyopathyMatthias Paul, Kambiz Rahbar, Joachim Gerss, et al.
EMBO Molecular Medicine|June 29, 2014
Gain-of-function mutation in TASK-4 channels and severe cardiac conduction disorderCorinna Friedrich, Susanne Rinné, Sven Zumhagen, et al.
The Journal of Clinical Investigation|September 4, 2009
Impaired endocytosis of the ion channel TRPM4 is associated with human progressive familial heart block type IMartin Kruse, Eric Schulze-Bahr, Valerie Corfield, et al.
Cardiovascular Research|July 26, 2005
Substitution of a conserved alanine in the domain IIIS4-S5 linker of the cardiac sodium channel causes long QT syndromeJeroen P P Smits, Marieke W Veldkamp, Connie R Bezzina, et al.
Plos One|July 6, 2016
Improved Clinical Risk Stratification in Patients with Long QT Syndrome? Novel Insights from Multi-Channel ECGsAlexander Samol, Mehmet Gönes, Sven Zumhagen, et al.
Pageof 16