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Gruppiert nach: Dokumententyp | Veröffentlichungsdatum
Springe zu: 2024 | 2023 | 2022 | 2020 | 2019 | 2018
Anzahl der Publikationen: 9

2024

Ye, Lan; Greten, Stephan; Wegner, Florian; Doll-Lee, Johanna; Krey, Lea; Heine, Johanne; Gandor, Florin; Vogel, Annemarie; Berger, Luise; Gruber, Doreen; Levin, Johannes; Katzdobler, Sabrina; Peters, Oliver; Dashti, Eman; Priller, Josef; Spruth, Eike Jakob; Kuehn, Andrea A.; Krause, Patricia; Spottke, Annika; Schneider, Anja; Beyle, Aline; Kimmich, Okka; Donix, Markus; Haussmann, Robert; Brandt, Moritz; Dinter, Elisabeth; Wiltfang, Jens; Schott, Bjoern H.; Zerr, Inga; Baehr, Mathias; Buerger, Katharina; Janowitz, Daniel; Perneczky, Robert; Rauchmann, Boris-Stephan; Weidinger, Endy; Duezel, Emrah; Glanz, Wenzel; Teipel, Stefan; Kilimann, Ingo; Wurster, Isabel; Brockmann, Kathrin; Hoffmann, Daniel C.; Klockgether, Thomas; Krause, Olaf; Heck, Johannes; Hoeglinger, Guenter U. und Klietz, Martin (2024): The comorbidity profiles and medication issues of patients with multiple system atrophy: a systematic cross-sectional analysis. In: Journal of Neurology, Bd. 271, Nr. 5: S. 2639-2648 [PDF, 4MB]

Greten, Stephan; Wegner, Florian; Jensen, Ida; Krey, Lea; Rogozinski, Sophia; Fehring, Meret; Heine, Johanne; Doll-Lee, Johanna; Poetter-Nerger, Monika; Zeitzschel, Molly; Hagena, Keno; Pedrosa, David J.; Eggers, Carsten; Buerk, Katrin; Trenkwalder, Claudia; Claus, Inga; Warnecke, Tobias; Suess, Patrick; Winkler, Juergen; Gruber, Doreen; Gandor, Florin; Berg, Daniela; Paschen, Steffen; Classen, Joseph; Pinkhardt, Elmar H.; Kassubek, Jan; Jost, Wolfgang H.; Toenges, Lars; Kuehn, Andrea A.; Schwarz, Johannes; Peters, Oliver; Dashti, Eman; Priller, Josef; Spruth, Eike J.; Krause, Patricia; Spottke, Annika; Schneider, Anja; Beyle, Aline; Kimmich, Okka; Donix, Markus; Haussmann, Robert; Brandt, Moritz; Dinter, Elisabeth; Wiltfang, Jens; Schott, Bjoern H.; Zerr, Inga; Baehr, Mathias; Buerger, Katharina; Janowitz, Daniel; Perneczky, Robert; Rauchmann, Boris-Stephan; Weidinger, Endy; Levin, Johannes; Katzdobler, Sabrina; Duezel, Emrah; Glanz, Wenzel; Teipel, Stefan; Kilimann, Ingo; Prudlo, Johannes; Gasser, Thomas; Brockmann, Kathrin; Hoffmann, Daniel C.; Klockgether, Thomas; Krause, Olaf; Heck, Johannes; Hoeglinger, Guenter U. und Klietz, Martin (2024): The comorbidity and co-medication profile of patients with progressive supranuclear palsy. In: Journal of Neurology, Bd. 271, Nr. 2: S. 782-793 [PDF, 1MB]

2023

Buchert, Ralph; Wegner, Florian; Huppertz, Hans-Juergen; Berding, Georg; Brendel, Matthias; Apostolova, Ivayla; Buhmann, Carsten; Dierks, Alexander; Katzdobler, Sabrina; Klietz, Martin; Levin, Johannes; Mahmoudi, Nima; Rinscheid, Andreas; Rogozinski, Sophia; Rumpf, Jost-Julian; Schneider, Christine; Stoecklein, Sophia; Spetsieris, Phoebe G.; Eidelberg, David; Wattjes, Mike P.; Sabri, Osama; Barthel, Henryk und Hoeglinger, Guenter (2023): Automatic covariance pattern analysis outperforms visual reading of 18F-fluorodeoxyglucose-positron emission tomography (FDG-PET) in variant progressive supranuclear palsy. In: Movement Disorders, Bd. 38, Nr. 10: S. 1901-1913 [PDF, 1MB]

Wattjes, Mike; Huppertz, Hans-Juergen; Mahmoudi, Nima; Stoecklein, Sophia; Rogozinski, Sophia; Wegner, Florian; Klietz, Martin; Apostolova, Ivayla; Levin, Johannes; Katzdobler, Sabrina; Buhmann, Carsten; Quattrone, Andrea; Berding, Georg; Brendel, Matthias; Barthel, Henryk; Sabri, Osama; Hoeglinger, Guenter und Buchert, Ralph (2023): Brain MRI in Progressive Supranuclear Palsy with Richardson's Syndrome and Variant Phenotypes. In: Movement Disorders, Bd. 38, Nr. 10: S. 1891-1900 [PDF, 809kB]

2022

Klietz, Martin; Katzdobler, Sabrina; Levin, Johannes; Wegner, Florian; Hoellerhage, Matthias; Hopfner, Franziska; Krey, Lea; Heine, Johanne; Skripuletz, Thomas und Hoeglinger, Guenter U. (2022): HOMER-3 Antibodies Were Not Detected in Two German Cohorts of Patients with Multiple System Atrophy. In: Movement Disorders, Bd. 37, Nr. 10: S. 2165-2166 [PDF, 119kB]

2020

Piot, Ines; Schweyer, Kerstin; Respondek, Gesine; Stamelou, Maria; Gasser, Thomas; Hermann, Andreas; Höglinger, Gunter; Hoellerhage, Matthias; Kimmich, Okka; Klockgether, Thomas; Levin, Johannes; Machetanz, Gerrit; Osterrath, Antje; Palleis, Carla; Prudlo, Johannes; Spottke, Annika; Berg, Daniela; Buerk, Katrin; Classen, Joseph; Eggers, Carsten; Greuel, Andrea; Grimm, Max-Joseph; Hermann, Lennard; Iankova, Vassilena; Jahn, Klaus; Jost, Wolfgang; Klietz, Martin; Kuehn, Andrea; Marxreiter, Franz; Paschen, Steffen; Poetter-Nerger, Monika; Preisl, Marie-Therese; Prilop, Lisa; Toenges, Lars; Trenkwalder, Claudia; Warnecke, Tobias; Wegner, Florian; Winkler, Jürgen; Antonini, Angelo; Bhatia, Kailash P.; Boxer, Adam L.; Colosimo, Carlo; Compta, Yaroslau; Corvol, Jean-Christophe; Golbe, Lawrence I.; Hoglinger, Guenter U.; Lang, Anthony E.; Litvan, Irene; Morris, Huw R.; Nilsson, Christer; Pantelyat, Alexander; Respondek, Gesine; Stamelou, Maria; Sckopke, Philipp; Schenk, Thomas; Goetz, Christopher G. und Stebbins, Glenn T. (2020): The Progressive Supranuclear Palsy Clinical Deficits Scale. In: Movement Disorders, Bd. 35, Nr. 4: S. 650-661

Abo-Rady, Masin; Kalmbach, Norman; Pal, Arun; Schludi, Carina; Janosch, Antje; Richter, Tanja; Freitag, Petra; Bickle, Marc; Kahlert, Anne-Karin; Petri, Susanne; Stefanov, Stefan; Glass, Hannes; Staege, Selma; Just, Walter; Bhatnagar, Rajat; Edbauer, Dieter; Hermann, Andreas; Wegner, Florian und Sterneckert, Jared L. (2020): Knocking out C9ORF72 Exacerbates Axonal Trafficking Defects Associated with Hexanucleotide Repeat Expansion and Reduces Levels of Heat Shock Proteins. In: Stem Cell Reports, Bd. 14, Nr. 3: S. 390-405 [PDF, 19MB]

2019

Naumann, Marcel; Peikert, Kevin; Guenther, Rene; van der Kooi, Anneke J.; Aronica, Eleonora; Huebers, Annemarie; Danel, Veronique; Corcia, Philippe; Pan-Montojo, Francisco; Cirak, Sebahattin; Haliloglu, Goeknur; Ludolph, Albert C.; Goswami, Anand; Andersen, Peter M.; Prudlo, Johannes; Wegner, Florian; Van Damme, Philip; Weishaupt, Jochen H. und Hermann, Andreas (2019): Phenotypes and malignancy risk of different FUS mutations in genetic amyotrophic lateral sclerosis. In: Annals of Clinical and Translational Neurology [PDF, 626kB]

2018

Naumann, Marcel; Pal, Arun; Goswami, Anand; Lojewski, Xenia; Japtok, Julia; Vehlow, Anne; Naujock, Maximilian; Günther, Rene; Jin, Mengmeng; Stanslowsky, Nancy; Reinhardt, Peter; Sterneckert, Jared; Frickenhaus, Marie; Pan-Montojo, Francisco; Storkebaum, Erik; Poser, Ina; Freischmidt, Axel; Weishaupt, Jochen H.; Holzmann, Karlheinz; Troost, Dirk; Ludolph, Albert C.; Böckers, Tobias M.; Liebau, Stefan; Petri, Susanne; Cordes, Nils; Hyman, Anthony A.; Wegner, Florian; Grill, Stephan W.; Weis, Joachim; Storch, Alexander und Hermann, Andreas (2018): Impaired DNA damage response signaling by FUS-NLS mutations leads to neurodegeneration and FUS aggregate formation. In: Nature Communications, Bd. 9, 335 [PDF, 6MB]

Diese Liste wurde am Sat Nov 16 22:56:41 2024 CET erstellt.