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Functional characterization of novel alpha-helical rod domain desmin (DES) pathogenic variants associated with dilated cardiomyopathy, atrioventricular block and a risk for sudden cardiac death Fischer B, Dittmann S, Brodehl A, Unger A, Stallmeyer B, Paul M, Seebohm G, Kayser A, Peischard S, Linke WA, Milting H, Schulze-Bahr E. (2021) In: International Journal of Cardiology, 329. Forschungsartikel (Zeitschrift)
Long, longer, long QT syndrome: what makes the difference? Dittmann S, Kayser A, Schulze-Bahr E. (2021) In: ((Bitte Journal prüfen)), 117. Forschungsartikel (Zeitschrift)
A rare cause of sudden unexpected death syndrome (SUDS) in the first year of life: endomyocardial fibroelastosis (EFE) due to two compound heterozygous MYBPC3 mutations Hartung B, Tank A, Dittmann S, Ritz-Timme S, Schulze-Bahr E. (2021) In: ((Bitte Journal prüfen)), 21. Forschungsartikel (Zeitschrift)
Impact of presynaptic sympathetic imbalance in long-QT syndrome by positron emission tomography Zumhagen S, Vrachimis A, Stegger L, Kies P, Wenning C, Ernsting M, Muller J, Seebohm G, Paul M, Schafers K, Stallmeyer B, Schafers M, Schulze-Bahr E (2018) In: Heart, 104(4). Forschungsartikel (Zeitschrift)
Sodium permeable and "hypersensitive" TREK-1 channels cause ventricular tachycardia Decher N, Ortiz-Bonnin B, Friedrich C, Schewe M, Kiper AK, Rinne S, Seemann G, Peyronnet R, Zumhagen S, Bustos D, Kockskamper J, Kohl P, Just S, Gonzalez W, Baukrowitz T, Stallmeyer B, Schulze-Bahr E (2017) In: ((Bitte Journal prüfen)), 9(4). Forschungsartikel (Zeitschrift)
Deconstruction - reconstruction approach to analyze the essential structural elements of tetrahydro-3-benzazepine-based antagonists of GluN2B subunit containing NMDA receptors Dey S, Temme L, Schreiber JA, Schepmann D, Frehland B, Lehmkuhl K, Strutz-Seebohm N, Seebohm G, Wunsch B (2017) In: ((Bitte Journal prüfen)), 138.
Design, Synthesis, Pharmacological Evaluation and Docking Studies of GluN2B-Selective NMDA Receptor Antagonists with a Benzo[7]annulen-7-amine Scaffold In: .
Through modulation of cardiac Ca(2+) handling, UCP2 affects cardiac electrophysiology and influences the susceptibility for Ca(2+) -mediated arrhythmias In: .
Generation and cardiac subtype-specific differentiation of PITX2-deficient human iPS cell lines for exploring familial atrial fibrillation In: .
Cardiac Subtype-Specific Modeling of Kv1.5 Ion Channel Deficiency Using Human Pluripotent Stem Cells In: .