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Eric Schulze

Showing results (71-80 of 155) with videos related to

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Circulation. Arrhythmia and Electrophysiology|October 8, 2009
Absence of pathognomonic or inflammatory patterns in cardiac biopsies from patients with Brugada syndromeSven Zumhagen, Tilmann Spieker, Julia Rolinck, et al.
European Heart Journal|August 3, 2006
Electrocardiographic risk stratification in families with congenital long QT syndromeGerold Mönnig, Lars Eckardt, Horst Wedekind, et al.
Journal of Molecular Medicine (Berlin, Germany)|August 20, 2002
Identification and functional characterization of a novel KCNE2 (MiRP1) mutation that alters HERG channel kineticsDirk Isbrandt, Patrick Friederich, Anna Solth, et al.
International Journal of Legal Medicine|July 14, 2005
Sudden infant death syndrome and long QT syndrome: an epidemiological and genetic studyHorst Wedekind, Thomas Bajanowski, Patrick Friederich, et al.
Journal of Nuclear Medicine : Official Publication, Society of Nuclear Medicine|September 13, 2011
Cardiac sympathetic dysfunction in genotyped patients with arrhythmogenic right ventricular cardiomyopathy and risk of recurrent ventricular tachyarrhythmiasMatthias Paul, Thomas Wichter, Peter Kies, et al.
Circulation|February 13, 2002
Cardiac autonomic dysfunction in Brugada syndromeThomas Wichter, Peter Matheja, Lars Eckardt, et al.
Frontiers in Cardiovascular Medicine|June 5, 2023
Cardiomyopathy related desmocollin-2 prodomain variants affect the intracellular cadherin transport and processingGreta Marie Pohl, Manuel Göz, Anna Gaertner, et al.
Heart Rhythm|April 21, 2005
Implantable cardioverter-defibrillator therapy in patients with congenital long-QT syndrome: a long-term follow-upGerold Mönnig, Julia Köbe, Andreas Löher, et al.
Herzschrittmachertherapie & Elektrophysiologie|February 19, 2014
[Brugada syndrome. Current clinical aspects and risk stratification]Lars Eckardt, Sascha Rolf, Gerold Mönnig, et al.
Circulation. Genomic and Precision Medicine|January 16, 2019
Familial Sinus Node Disease Caused by a Gain of GIRK (G-Protein Activated Inwardly Rectifying K<sup>+</sup> Channel) Channel FunctionJohanna Kuß, Birgit Stallmeyer, Matthias Goldstein, et al.
Pageof 16

Showing results (71-80 of 155) with videos related to

Sort By:
Pageof 16
Circulation. Arrhythmia and Electrophysiology|October 8, 2009
Absence of pathognomonic or inflammatory patterns in cardiac biopsies from patients with Brugada syndromeSven Zumhagen, Tilmann Spieker, Julia Rolinck, et al.
European Heart Journal|August 3, 2006
Electrocardiographic risk stratification in families with congenital long QT syndromeGerold Mönnig, Lars Eckardt, Horst Wedekind, et al.
Journal of Molecular Medicine (Berlin, Germany)|August 20, 2002
Identification and functional characterization of a novel KCNE2 (MiRP1) mutation that alters HERG channel kineticsDirk Isbrandt, Patrick Friederich, Anna Solth, et al.
International Journal of Legal Medicine|July 14, 2005
Sudden infant death syndrome and long QT syndrome: an epidemiological and genetic studyHorst Wedekind, Thomas Bajanowski, Patrick Friederich, et al.
Journal of Nuclear Medicine : Official Publication, Society of Nuclear Medicine|September 13, 2011
Cardiac sympathetic dysfunction in genotyped patients with arrhythmogenic right ventricular cardiomyopathy and risk of recurrent ventricular tachyarrhythmiasMatthias Paul, Thomas Wichter, Peter Kies, et al.
Circulation|February 13, 2002
Cardiac autonomic dysfunction in Brugada syndromeThomas Wichter, Peter Matheja, Lars Eckardt, et al.
Frontiers in Cardiovascular Medicine|June 5, 2023
Cardiomyopathy related desmocollin-2 prodomain variants affect the intracellular cadherin transport and processingGreta Marie Pohl, Manuel Göz, Anna Gaertner, et al.
Heart Rhythm|April 21, 2005
Implantable cardioverter-defibrillator therapy in patients with congenital long-QT syndrome: a long-term follow-upGerold Mönnig, Julia Köbe, Andreas Löher, et al.
Herzschrittmachertherapie & Elektrophysiologie|February 19, 2014
[Brugada syndrome. Current clinical aspects and risk stratification]Lars Eckardt, Sascha Rolf, Gerold Mönnig, et al.
Circulation. Genomic and Precision Medicine|January 16, 2019
Familial Sinus Node Disease Caused by a Gain of GIRK (G-Protein Activated Inwardly Rectifying K<sup>+</sup> Channel) Channel FunctionJohanna Kuß, Birgit Stallmeyer, Matthias Goldstein, et al.
Pageof 16