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Anzahl der Publikationen: 5
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]
Yilmaz, Ruestem; Mueller, Kathrin; Brenner, David; Volk, Alexander E.; Borck, Guntram; Hermann, Andreas; Meitinger, Thomas; Strom, Tim M.; Danzer, Karin M.; Ludolph, Albert C.; Andersen, Peter M. und Weishaupt, Jochen H.
(2020):
SQSTM1/p62 variants in 486 patients with familial ALS from Germany and Sweden.
In: Neurobiology of Aging, Bd. 87
Brenner, David; Rosenbohm, Angela; Yilmaz, Ruestem; Mueller, Kathrin; Grehl, Torsten; Petri, Susanne; Meyer, Thomas; Grosskreutz, Julian; Weydt, Patrick; Ruf, Wolfgang; Neuwirth, Christoph; Weber, Markus; Pinto, Susana; Claeys, Kristl G.; Schrank, Berthold; Jordan, Berit; Knehr, Antje; Guenther, Kornelia; Huebers, Annemarie; Zeller, Daniel; Kubisch, Christian; Jablonka, Sibylle; Sendtner, Michael; Klopstock, Thomas; de Carvalho, Mamede; Sperfeld, Anne; Borck, Guntram; Volk, Alexander E.; Dorst, Johannes; Weis, Joachim; Otto, Markus; Schuster, Joachim; Del Tredici, Kelly; Braak, Heiko; Danzer, Karin M.; Freischmidt, Axel; Meitinger, Thomas; Ludolph, Albert C.; Andersen, Peter M.; Weishaupt, Jochen H.; Weyen, Ute; Hermann, Andreas; Winkler, Juergen; Hagenacker, Tim; Koch, Jan Christoph; Lingor, Paul; Goericke, Bettina; Zierz, Stephan; Baum, Petra; Wolf, Joachim; Winkler, Andrea; Young, Peter; Bogdahn, Ulrich; Prudlo, Johannes und Kassubek, Jan
(2019):
Reply: Adult-onset distal spinal muscular atrophy: a new phenotype associated with KIF5A mutations.
In: Brain, Bd. 142, e67
[PDF, 190kB]
Forouhideh, Yalda; Mueller, Kathrin; Ruf, Wolfgang; Assi, Muhannad; Seker, Tuncay; Tunca, Ceren; Knehr, Antje; Strom, Tim M.; Gorges, Martin; Schradt, Falk; Meitinger, Thomas; Ludolph, Albert C.; Pinkhardt, Elmar H.; Basak, A. Nazli; Kassubek, Jan; Uttner, Ingo und Weishaupt, Jochen H.
(2019):
A biallelic mutation links MYORG to autosomal-recessive primary familial brain calcification.
In: Brain, Bd. 142
[PDF, 446kB]