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Britt Maria Beckmann

Showing results (1-10 of 36) with videos related to

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Herzschrittmachertherapie & Elektrophysiologie|September 21, 2012
[Genetic testing in hereditary arrythmia syndromes today and in the future]Britt-Maria Beckmann, Stefan Kääb
Herzschrittmachertherapie & Elektrophysiologie|January 10, 2024
[Postmortem genetic analysis following sudden cardiac death : Background, approach, and future]Silke Kauferstein, Britt-Maria Beckmann
Deutsches Arzteblatt International|October 7, 2011
Inherited cardiac arrhythmias: diagnosis, treatment, and preventionBritt-Maria Beckmann, Arne Pfeufer, Stefan Kääb
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|September 13, 2011
Recurrent torsades de pointes after catheter ablation of incessant ventricular bigeminy in combination with QT prolongationChristopher Reithmann, Michael Fiek, Britt-Maria Beckmann, et al.
Innere Medizin (Heidelberg, Germany)|July 11, 2025
[Molecular autopsy: post-mortem genetic testing following sudden cardiac death]Tina Jenewein, Britt-Maria Beckmann, Stefanie Scheiper-Welling, et al.
BMC Medical Genetics|October 12, 2017
Characterization of a novel KCNJ2 sequence variant detected in Andersen-Tawil syndrome patientsStefanie Scheiper, Brigitte Hertel, Britt-Maria Beckmann, et al.
International Journal of Molecular Sciences|January 27, 2021
Molecular Mechanism of Autosomal Recessive Long QT-Syndrome 1 without DeafnessAnnemarie Oertli, Susanne Rinné, Robin Moss, et al.
BMC Medical Genetics|November 20, 2020
Characterization of an N-terminal Na<sub>v</sub>1.5 channel variant - a potential risk factor for arrhythmias and sudden death?Stefanie Scheiper-Welling, Paolo Zuccolini, Oliver Rauh, et al.
Journal of Clinical Medicine|December 11, 2022
Fetal Bradycardia Caused by Monogenic Disorders-A Review of the LiteratureDominik S Westphal, Michael Hauser, Britt-Maria Beckmann, et al.
Forensic Science International|May 5, 2017
Relevance of molecular testing in patients with a family history of sudden deathSilke Kauferstein, Nadine Herz, Stefanie Scheiper, et al.
Pageof 4

Showing results (1-10 of 36) with videos related to

Sort By:
Pageof 4
Herzschrittmachertherapie & Elektrophysiologie|September 21, 2012
[Genetic testing in hereditary arrythmia syndromes today and in the future]Britt-Maria Beckmann, Stefan Kääb
Herzschrittmachertherapie & Elektrophysiologie|January 10, 2024
[Postmortem genetic analysis following sudden cardiac death : Background, approach, and future]Silke Kauferstein, Britt-Maria Beckmann
Deutsches Arzteblatt International|October 7, 2011
Inherited cardiac arrhythmias: diagnosis, treatment, and preventionBritt-Maria Beckmann, Arne Pfeufer, Stefan Kääb
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|September 13, 2011
Recurrent torsades de pointes after catheter ablation of incessant ventricular bigeminy in combination with QT prolongationChristopher Reithmann, Michael Fiek, Britt-Maria Beckmann, et al.
Innere Medizin (Heidelberg, Germany)|July 11, 2025
[Molecular autopsy: post-mortem genetic testing following sudden cardiac death]Tina Jenewein, Britt-Maria Beckmann, Stefanie Scheiper-Welling, et al.
BMC Medical Genetics|October 12, 2017
Characterization of a novel KCNJ2 sequence variant detected in Andersen-Tawil syndrome patientsStefanie Scheiper, Brigitte Hertel, Britt-Maria Beckmann, et al.
International Journal of Molecular Sciences|January 27, 2021
Molecular Mechanism of Autosomal Recessive Long QT-Syndrome 1 without DeafnessAnnemarie Oertli, Susanne Rinné, Robin Moss, et al.
BMC Medical Genetics|November 20, 2020
Characterization of an N-terminal Na<sub>v</sub>1.5 channel variant - a potential risk factor for arrhythmias and sudden death?Stefanie Scheiper-Welling, Paolo Zuccolini, Oliver Rauh, et al.
Journal of Clinical Medicine|December 11, 2022
Fetal Bradycardia Caused by Monogenic Disorders-A Review of the LiteratureDominik S Westphal, Michael Hauser, Britt-Maria Beckmann, et al.
Forensic Science International|May 5, 2017
Relevance of molecular testing in patients with a family history of sudden deathSilke Kauferstein, Nadine Herz, Stefanie Scheiper, et al.
Pageof 4