Britt-Maria Beckmann

Affiliations: 
Cardiology LMU Munich, München, Bayern, Germany 
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Stefan Kaab research scientist LMU Munich

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Aline D. Scherff research assistant 2014-2020 LMU Munich
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Publications

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Barkauskas R, Jenewein T, Scheiper-Welling S, et al. (2024) From rare events to systematic data collection: the RESCUED registry for sudden cardiac death in the young in Germany. Clinical Research in Cardiology : Official Journal of the German Cardiac Society
Yeruva S, Stangner K, Jungwirth A, et al. (2023) Correction: Catalytic antibodies in arrhythmogenic cardiomyopathy patients cleave desmoglein 2 and N-cadherin and impair cardiomyocyte cohesion. Cellular and Molecular Life Sciences : Cmls. 80: 296
Neumann B, Vink AS, Hermans BJM, et al. (2023) Manual versus Automatic Assessment of the QT-Interval and QTc. 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
Yeruva S, Stangner K, Jungwirth A, et al. (2023) Catalytic antibodies in arrhythmogenic cardiomyopathy patients cleave desmoglein 2 and N-cadherin and impair cardiomyocyte cohesion. Cellular and Molecular Life Sciences : Cmls. 80: 203
Rinné S, Oertli A, Nagel C, et al. (2023) Functional Characterization of a Spectrum of Novel Romano-Ward Syndrome Variants. International Journal of Molecular Sciences. 24
Barc J, Tadros R, Glinge C, et al. (2022) Author Correction: Genome-wide association analyses identify new Brugada syndrome risk loci and highlight a new mechanism of sodium channel regulation in disease susceptibility. Nature Genetics
Barc J, Tadros R, Glinge C, et al. (2022) Genome-wide association analyses identify new Brugada syndrome risk loci and highlight a new mechanism of sodium channel regulation in disease susceptibility. Nature Genetics
Oertli A, Rinné S, Moss R, et al. (2021) Molecular Mechanism of Autosomal Recessive Long QT-Syndrome 1 without Deafness. International Journal of Molecular Sciences. 22
Scheiper-Welling S, Zuccolini P, Rauh O, et al. (2020) Characterization of an N-terminal Na1.5 channel variant - a potential risk factor for arrhythmias and sudden death? Bmc Medical Genetics. 21: 227
Siebermair J, Lehner S, Sattler SM, et al. (2020) Left-ventricular innervation assessed by I-SPECT/CT is associated with cardiac events in inherited arrhythmia syndromes. International Journal of Cardiology
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