Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

W Haverkamp

Showing results (131-140 of 165) with videos related to

Pageof 17
Sort By:
Human Genetics|October 28, 1997
Autosomal recessive long-QT syndrome (Jervell Lange-Nielsen syndrome) is genetically heterogeneousE Schulze-Bahr, W Haverkamp, H Wedekind, et al.
Journal of Molecular Medicine (Berlin, Germany)|November 1, 1995
Molecular analysis at the Harvey Ras-1 gene in patients with long QT syndromeE Schulze-Bahr, W Haverkamp, H Wiebusch, et al.
Zeitschrift Fur Kardiologie|January 1, 1994
[The pro-arrhythmic effects of anti-arrhythmia agents]W Haverkamp, T Wichter, X Chen, et al.
Herz|November 1, 2016
New implantable cardiac monitor with three-lead ECG and active noise detectionJ Lauschke, M Busch, W Haverkamp, et al.
Acta Cardiologica|October 4, 2016
Managing periprocedural anticoagulation therapy in patients undergoing device implantation: survey in Germany, Austria and SwitzerlandF Blaschke, P Lacour, A Wutzler, et al.
Naunyn-Schmiedeberg'S Archives of Pharmacology|May 2, 2001
Blocking effects of the antiarrhythmic drug propafenone on the HERG potassium channelJ Mergenthaler, W Haverkamp, A Hüttenhofer, et al.
Zeitschrift Fur Kardiologie|December 1, 1993
[Torsade de pointes]W Haverkamp, M Hördt, X Chen, et al.
Journal of Molecular Medicine (Berlin, Germany)|November 3, 2001
A novel long-QT 5 gene mutation in the C-terminus (V109I) is associated with a mild phenotypeE Schulze-Bahr, M Schwarz, S Hauenschild, et al.
Journal of Cardiovascular Electrophysiology|August 1, 1994
Recurrence and late block of accessory pathway conduction following radiofrequency catheter ablationX Chen, H Kottkamp, G Hindricks, et al.
European Heart Journal|January 1, 1994
Role of programmed ventricular stimulation in patients with idiopathic dilated cardiomyopathy and documented sustained ventricular tachyarrhythmias: inducibility and prognostic value in 102 patientsX Chen, M Shenasa, M Borggrefe, et al.
Pageof 17

Showing results (131-140 of 165) with videos related to

Sort By:
Pageof 17
Human Genetics|October 28, 1997
Autosomal recessive long-QT syndrome (Jervell Lange-Nielsen syndrome) is genetically heterogeneousE Schulze-Bahr, W Haverkamp, H Wedekind, et al.
Journal of Molecular Medicine (Berlin, Germany)|November 1, 1995
Molecular analysis at the Harvey Ras-1 gene in patients with long QT syndromeE Schulze-Bahr, W Haverkamp, H Wiebusch, et al.
Zeitschrift Fur Kardiologie|January 1, 1994
[The pro-arrhythmic effects of anti-arrhythmia agents]W Haverkamp, T Wichter, X Chen, et al.
Herz|November 1, 2016
New implantable cardiac monitor with three-lead ECG and active noise detectionJ Lauschke, M Busch, W Haverkamp, et al.
Acta Cardiologica|October 4, 2016
Managing periprocedural anticoagulation therapy in patients undergoing device implantation: survey in Germany, Austria and SwitzerlandF Blaschke, P Lacour, A Wutzler, et al.
Naunyn-Schmiedeberg'S Archives of Pharmacology|May 2, 2001
Blocking effects of the antiarrhythmic drug propafenone on the HERG potassium channelJ Mergenthaler, W Haverkamp, A Hüttenhofer, et al.
Zeitschrift Fur Kardiologie|December 1, 1993
[Torsade de pointes]W Haverkamp, M Hördt, X Chen, et al.
Journal of Molecular Medicine (Berlin, Germany)|November 3, 2001
A novel long-QT 5 gene mutation in the C-terminus (V109I) is associated with a mild phenotypeE Schulze-Bahr, M Schwarz, S Hauenschild, et al.
Journal of Cardiovascular Electrophysiology|August 1, 1994
Recurrence and late block of accessory pathway conduction following radiofrequency catheter ablationX Chen, H Kottkamp, G Hindricks, et al.
European Heart Journal|January 1, 1994
Role of programmed ventricular stimulation in patients with idiopathic dilated cardiomyopathy and documented sustained ventricular tachyarrhythmias: inducibility and prognostic value in 102 patientsX Chen, M Shenasa, M Borggrefe, et al.
Pageof 17