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1

Atrial Arrhythmias in Long-QT Syndrome under Daily Life Conditions: A Nested Case Control Study

STEPHAN ZELLERHOFF, RUDIN PISTULLI, GEROLD MÖNNIG, MARTIN HINTERSEER, BRITT-MARIA BECKMANN, JULIA KÖBE, GERHARD STEINBECK, STEFAN KÄÄB, WILHELM HAVERKAMP, LARISSA FABRITZ, RAINER GRADAUS, GÜNTER BREIT

Journal:

Journal of Cardiovascular Electrophysiology

Year:

2009

Language:

english

File:

PDF, 162 KB

english, 2009

2

Relation of Increased Short-Term Variability of QT Interval to Congenital Long-QT Syndrome

Martin Hinterseer, Britt-Maria Beckmann, Morten B. Thomsen, Arne Pfeufer, Robert Dalla Pozza, Markus Loeff, Heinrich Netz, Gerhard Steinbeck, Marc A. Vos, Stefan Kääb

Journal:

The American Journal of Cardiology

Year:

2009

Language:

english

File:

PDF, 244 KB

english, 2009

3

Usefulness of Short-Term Variability of QT Intervals as a Predictor for Electrical Remodeling and Proarrhythmia in Patients With Nonischemic Heart Failure

Martin Hinterseer, Britt-Maria Beckmann, Morten B. Thomsen, Arne Pfeufer, Michael Ulbrich, Moritz F. Sinner, Siegfried Perz, H.-Erich Wichmann, Csaba Lengyel, Rainer Schimpf, Sebastian K.G. Maier, And

Journal:

The American Journal of Cardiology

Year:

2010

Language:

english

File:

PDF, 430 KB

english, 2010

4

Laminopathy presenting as familial atrial fibrillation

Britt Maria Beckmann, Elke Holinski-Feder, Maggie C. Walter, Nadine Haserück, Christopher Reithmann, Martin Hinterseer, Arthur A. Wilde, Stefan Kääb

Journal:

International Journal of Cardiology

Year:

2010

Language:

english

File:

PDF, 214 KB

english, 2010

5

Seizures on hearing the alarm clock

Christian Vollmar, Berend Feddersen, Britt Maria Beckmann, Stefan Kääb, Soheyl Noachtar

Journal:

Year:

2008

Language:

english

File:

PDF, 110 KB

english, 2008

6

Molekulargenetische Diagnostik bei hereditären Arrhythmiesyndromen heute und in Zukunft

Beckmann, Britt-Maria, Kääb, Stefan

Journal:

Herzschrittmachertherapie und Elektrophysiologie

Year:

2012

Language:

german

File:

PDF, 792 KB

german, 2012

7

Clinical utility gene card for: Long-QT Syndrome (types 1–13)

Beckmann, Britt-Maria, Wilde, Arthur A M, Kääb, Stefan

Journal:

European Journal of Human Genetics

Year:

2013

Language:

english

File:

PDF, 191 KB

english, 2013

8

A meta-analysis of genome-wide association studies of the electrocardiographic early repolarization pattern

Sinner, Moritz F., Porthan, Kimmo, Noseworthy, Peter A., Havulinna, Aki S., Tikkanen, Jani T., MÃ¼ller-Nurasyid, Martina, Peloso, Gina, Ulivi, Sheila, Beckmann, Britt Maria, Brockhaus, A. Catharina, C

Journal:

Year:

2012

Language:

english

File:

PDF, 950 KB

english, 2012

9

P5-30

Hinterseer, Martin, Beckmann, Britt-Maria, Thomsen, Morten B., Pfeufer, Arne, Perz, Siegfried, Wichmann, H. Erich, Steinbeck, Gerhard, Vos, Marc A., Kääb, Stefan

Journal:

Year:

2006

Language:

english

File:

PDF, 88 KB

english, 2006

10

Lack of replication in polymorphisms reported to be associated with atrial fibrillation

Sinner, Moritz F., Lubitz, Steven A., Pfeufer, Arne, Makino, Seiko, Beckmann, Britt-Maria, Lunetta, Kathryn L., Steinbeck, Gerhard, Perz, Siegfried, Rahman, Rosanna, Sonni, Akshata

Journal:

Year:

2011

Language:

english

File:

PDF, 476 KB

english, 2011

11

Association of Early Repolarization Pattern on ECG with Risk of Cardiac and All-Cause Mortality: A Population-Based Prospective Cohort Study (MONICA/KORA)

Sinner, Moritz F., Reinhard, Wibke, Müller, Martina, Beckmann, Britt-Maria, Martens, Eimo, Perz, Siegfried, Pfeufer, Arne, Winogradow, Janina, Stark, Klaus, Meisinger, Christa, Wichmann, H.-Erich, Pet

Journal:

Year:

2010

Language:

english

File:

PDF, 359 KB

english, 2010

12

Genetische Arrhythmiesyndrome ohne strukturelle Herzerkrankung

Beckmann, Britt-Maria, Kääb, Stefan

Journal:

Kardiologie up2date

Year:

2016

Language:

german

File:

PDF, 396 KB

german, 2016

13

Electrophysiological characterization of a large set of novel variants in theSCN5A-gene: identification of novel LQTS3 and BrS mutations

Ortiz-Bonnin, Beatriz, Rinné, Susanne, Moss, Robin, Streit, Anne K., Scharf, Michael, Richter, Katrin, Stöber, Anika, Pfeufer, Arne, Seemann, Gunnar, Kääb, Stefan, Beckmann, Britt-Maria, Decher, Niels

Journal:

Pflügers Archiv European Journal of Physiology

Year:

2016

Language:

english

File:

PDF, 1.28 MB

english, 2016

14

Genetische Arrhythmiesyndrome – Teil 2

Beckmann, Britt-Maria, Curta, Adrian, Kääb, Stefan

Journal:

Kardiologie up2date

Year:

2017

Language:

german

File:

PDF, 2.14 MB

german, 2017

15

Relevance of molecular testing in patients with a family history of sudden death

Kauferstein, Silke, Herz, Nadine, Scheiper, Stefanie, Biel, Stephanie, Jenewein, Tina, Kunis, Malte, Erkapic, Damir, Beckmann, Britt-Maria, Neumann, Thomas

Journal:

Forensic Science International

Year:

2017

Language:

english

File:

PDF, 317 KB

english, 2017

16

Characterization of a novel KCNJ2 sequence variant detected in Andersen-Tawil syndrome patients

Scheiper, Stefanie, Hertel, Brigitte, Beckmann, Britt-Maria, Kääb, Stefan, Thiel, Gerhard, Kauferstein, Silke

Journal:

BMC Medical Genetics

Year:

2017

Language:

english

File:

PDF, 2.65 MB

english, 2017

17

Inherited Cardiac Arrhythmias

Beckmann, Britt-Maria, Pfeufer, Arne, Kääb, Stefan

Journal:

Deutsches "{A}rzteblatt international

Year:

2011

Language:

english

File:

PDF, 597 KB

english, 2011

18

Bedeutung und Probleme bei der Anwendung des Gendiagnostikgesetzes im klinischen Alltag

Daunderer, Johannes, Ebermann, Thorsten, Beckmann, Britt-Maria

Journal:

Aktuelle Kardiologie

Year:

2018

Language:

german

File:

PDF, 97 KB

german, 2018

19

Sudden unexpected death in the young — Value of massive parallel sequencing in postmortem genetic analyses

Scheiper, Stefanie, Ramos-Luis, Eva, Blanco-Verea, Alejandro, Niess, Constanze, Beckmann, Britt-Maria, Schmidt, Ulrike, Kettner, Mattias, Geisen, Christof, Verhoff, Marcel A., Brion, Maria, Kauferstei

Journal:

Forensic Science International

Year:

2018

Language:

english

File:

PDF, 643 KB

english, 2018

20

Calmodulin mutations and life-threatening cardiac arrhythmias: insights from the International Calmodulinopathy Registry

Crotti, Lia, Spazzolini, Carla, Tester, David J, Ghidoni, Alice, Baruteau, Alban-Elouen, Beckmann, Britt-Maria, Behr, Elijah R, Bennett, Jeffrey S, Bezzina, Connie R, Bhuiyan, Zahurul A, Celiker, Alpa

Journal:

European Heart Journal

Year:

2019

Language:

english

File:

PDF, 998 KB

english, 2019

21

Left-ventricular innervation assessed by 123I-SPECT/CT is associated with cardiac events in inherited arrhythmia syndromes

Siebermair, Johannes, Lehner, Sebastian, Sattler, Stefan M., Rizas, Konstantinos D., Beckmann, Britt-Maria, Becker, Alexander, Schiller, Julia, Metz, Corona, Zacherl, Mathias, Vonderlin, Nadine, Rassa

Journal:

International Journal of Cardiology

Year:

2020

File:

PDF, 1.78 MB

2020

22

Characterization of an N-terminal Nav1.5 channel variant â a potential risk factor for arrhythmias and sudden death?

Scheiper-Welling, Stefanie, Zuccolini, Paolo, Rauh, Oliver, Beckmann, Britt-Maria, Geisen, Christof, Moroni, Anna, Thiel, Gerhard, Kauferstein, Silke

Journal:

BMC Medical Genetics

Year:

2020

File:

PDF, 1.38 MB

2020

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