Anzahl der Publikationen: 3
Zeitschriftenartikel
Miesbach, Wolfgang; Menne, Jan; Bommer, Martin; Schönermarck, Ulf; Feldkamp, Thorsten; Nitschke, Martin; Westhoff, Timm H.; Seibert, Felix S.; Woitas, Rainer; Sousa, Rui; Wolf, Michael; Walzer, Stefan und Schwander, Björn
(2019):
Incidence of acquired thrombotic thrombocytopenic purpura in Germany: a hospital level study.
In: Orphanet Journal of Rare Diseases, Bd. 14, Nr. 1, 260
Martin, Ruairidh; Maury, Philippe; Bisceglia, Caterina; Wong, Tom; Estner, Heidi; Meyer, Christian; Dallet, Corentin; Martin, Claire A.; Shi, Rui; Takigawa, Masateru; Rollin, Anne; Frontera, Antonio; Thompson, Nathaniel; Kitamura, Takeshi; Vlachos, Konstantinos; Wolf, Michael; Cheniti, Ghassen; Duchateau, Josselin; Massoulie, Gregoire; Pambrun, Thomas; Denis, Arnaud; Derval, Nicolas; Hocini, Meleze; Della Bella, Paolo; Haissaguerre, Michel; Jais, Pierre; Dubois, Remi und Sacher, Frederic
(2018):
Characteristics of Scar-Related Ventricular Tachycardia Circuits Using Ultra-High-Density Mapping: A Multi-Center Study.
In: Circulation-Arrhythmia and Electrophysiology, Bd. 11, Nr. 10, e006569
Minnerop, Martina; Kurzwelly, Delia; Wagner, Holger; Söhn, Anne S.; Reichbauer, Jennifer; Tao, Feifei; Rattay, Tim W.; Peitz, Michael; Rehbach, Kristina; Giorgetti, Alejandro; Pyle, Angela; Thiele, Holger; Altmüller, Janine; Timmann, Dagmar; Karaca, Ilker; Lennarz, Martina; Bäts, Jonathan; Hengel, Holger; Synofzik, Matthis; Atasu, Burcu; Feely, Shawna; Kennerson, Marina; Stendel, Claudia; Lindig, Tobias; Gonzalez, Michael A.; Stirnberg, Rüdiger; Sturm, Marc; Röske, Sandra; Jung, Johanna; Bauer, Peter; Lohmann, Ebba; Herms, Stefan; Heilmann-Heimbach, Stefanie; Nicholson, Garth; Mahanjah, Muhammad; Sharkia, Rajech; Carloni, Paolo; Brüstle, Oliver; Klopstock, Thomas; Mathews, Katherine D.; Shy, Michael E.; Jonghe, Peter de; Chinnery, Patrick F.; Horvath, Rita; Kohlhase, Jürgen; Schmitt, Ina; Wolf, Michael; Greschus, Susanne; Amunts, Katrin; Maier, Wolfgang; Schöls, Ludger; Nürnberg, Peter; Zuchner, Stephan; Klockgether, Thomas; Ramirez, Alfredo und Schüle, Rebecca
(2017):
Hypomorphic mutations in POLR3A are a frequent cause of sporadic and recessive spastic ataxia.
In: Brain, Bd. 140: S. 1561-1578
Diese Liste wurde am
Sat Nov 23 23:21:40 2024 CET
erstellt.