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Anzahl der Publikationen: 3
Zeitschriftenartikel
Wiesenfarth, Maximilian; Dorst, Johannes; Brenner, David; Elmas, Zeynep; Parlak, Oezlem; Uzelac, Zeljko; Kandler, Katharina; Mayer, Kristina; Weiland, Ulrike; Herrmann, Christine; Schuster, Joachim; Freischmidt, Axel; Mueller, Kathrin; Siebert, Reiner; Bachhuber, Franziska; Simak, Tatiana; Guenther, Kornelia; Froehlich, Elke; Knehr, Antje; Regensburger, Martin; German, Alexander; Petri, Susanne; Grosskreutz, Julian; Klopstock, Thomas; Reilich, Peter; Schoeberl, Florian; Hagenacker, Tim; Weyen, Ute; Guenther, Rene; Vidovic, Maximilian; Jentsch, Martin; Haarmeier, Thomas; Weydt, Patrick; Valkadinov, Ivan; Hesebeck-Brinckmann, Jasper; Conrad, Julian; Weishaupt, Jochen Hans; Schumann, Peggy; Koertvelyessy, Peter; Meyer, Thomas; Ruf, Wolfgang Philipp; Witzel, Simon; Senel, Makbule; Tumani, Hayrettin und Ludolph, Albert Christian
(2024):
Effects of tofersen treatment in patients with SOD1-ALS in a real-world setting - a 12-month multicenter cohort study from the German early access program.
In: Eclinicalmedicine, Bd. 69, 102495
[PDF, 1MB]
Wiesenfarth, Maximilian; Guenther, Kornelia; Mueller, Kathrin; Witzel, Simon; Weiland, Ulrike; Mayer, Kristina; Herrmann, Christine; Brenner, David; Schuster, Joachim; Freischmidt, Axel; Lule, Dorothee; Meyer, Thomas; Regensburger, Martin; Grehl, Torsten; Emmer, Alexander; Petri, Susanne; Grosskreutz, Julian; Roediger, Annekathrin; Steinbach, Robert; Klopstock, Thomas; Reilich, Peter; Schoeberl, Florian; Wolf, Joachim; Hagenacker, Tim; Weyen, Ute; Zeller, Daniel; Ludolph, Albert C. und Dorst, Johannes
(2023):
Clinical and genetic features of amyotrophic lateral sclerosis patients with C9orf72 mutations.
In: Brain Communications, Bd. 5, Nr. 2, fcad087
[PDF, 806kB]
Witzel, Simon; Wagner, Matias; Zhao, Chen; Kandler, Katharina; Graf, Elisabeth; Berutti, Riccardo; Oexle, Konrad; Brenner, David; Winkelmann, Juliane und Ludolph, Albert C.
(2022):
Fast versus slow disease progression in amyotrophic lateral sclerosis-clinical and genetic factors at the edges of the survival spectrum.
In: Neurobiology of Aging, Bd. 119: S. 117-126