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Anzahl der Publikationen: 5
Zeitschriftenartikel
Boer, Eva M. J. de 
ORCID: https://orcid.org/0000-0002-2629-2748; Vries, Bálint S. de ORCID: https://orcid.org/0000-0001-9102-7353; Hecke, Wim Van; Mühlebner, Angelika; Vincken, Koen L.; Mol, Christian P.; Rheenen, Wouter van; Westeneng, Henk-Jan; Veldink, Jan H. ORCID: https://orcid.org/0000-0001-5572-9657; Höglinger, Günter U. ORCID: https://orcid.org/0000-0001-7587-6187; Morris, Huw R. ORCID: https://orcid.org/0000-0002-5473-3774; Litvan, Irene ORCID: https://orcid.org/0000-0002-3485-3445; Raaphorst, Joost; Ticozzi, Nicola; Corcia, Philippe ORCID: https://orcid.org/0000-0002-1625-8845; Vandenberghe, Wim ORCID: https://orcid.org/0000-0002-9758-5062; Pijnenburg, Yolande A. L.; Seelaar, Harro ORCID: https://orcid.org/0000-0003-1989-7527; Ingre, Caroline ORCID: https://orcid.org/0000-0001-5327-7204; Damme, Philip Van ORCID: https://orcid.org/0000-0002-4010-2357; Berg, Leonard H. van den ORCID: https://orcid.org/0000-0002-5203-9674; Warrenburg, Bart P. C. van de ORCID: https://orcid.org/0000-0003-4412-1616 und Es, Michael A. van ORCID: https://orcid.org/0000-0002-7709-5883
(2025):
Diagnosing primary lateral sclerosis. A clinico-pathological study.
In: Journal of Neurology, Bd. 272, 46
ORCID: https://orcid.org/0000-0002-2629-2748; Vries, Bálint S. de ORCID: https://orcid.org/0000-0001-9102-7353; Hecke, Wim Van; Mühlebner, Angelika; Vincken, Koen L.; Mol, Christian P.; Rheenen, Wouter van; Westeneng, Henk-Jan; Veldink, Jan H. ORCID: https://orcid.org/0000-0001-5572-9657; Höglinger, Günter U. ORCID: https://orcid.org/0000-0001-7587-6187; Morris, Huw R. ORCID: https://orcid.org/0000-0002-5473-3774; Litvan, Irene ORCID: https://orcid.org/0000-0002-3485-3445; Raaphorst, Joost; Ticozzi, Nicola; Corcia, Philippe ORCID: https://orcid.org/0000-0002-1625-8845; Vandenberghe, Wim ORCID: https://orcid.org/0000-0002-9758-5062; Pijnenburg, Yolande A. L.; Seelaar, Harro ORCID: https://orcid.org/0000-0003-1989-7527; Ingre, Caroline ORCID: https://orcid.org/0000-0001-5327-7204; Damme, Philip Van ORCID: https://orcid.org/0000-0002-4010-2357; Berg, Leonard H. van den ORCID: https://orcid.org/0000-0002-5203-9674; Warrenburg, Bart P. C. van de ORCID: https://orcid.org/0000-0003-4412-1616 und Es, Michael A. van ORCID: https://orcid.org/0000-0002-7709-5883
(2025):
Diagnosing primary lateral sclerosis. A clinico-pathological study.
In: Journal of Neurology, Bd. 272, 46
Koch, Jan C; Leha, Andreas; Bidner, Helen; Cordts, Isabell; Dorst, Johannes; Günther, René; Zeller, Daniel; Braun, Nathalie; Metelmann, Moritz; Corcia, Philippe; Cruz, Elisa De La; Weydt, Patrick; Meyer, Thomas; Großkreutz, Julian; Soriani, Marie-Hélène; Attarian, Shahram; Weishaupt, Jochen H; Weyen, Ute; Kuttler, Josua; Zurek, Gabriela; Rogers, Mary-Louise; Feneberg, Emily; Deschauer, Marcus ORCID: https://orcid.org/0000-0001-6116-6790; Neuwirth, Christoph; Wuu, Joanne; Ludolph, Albert C; Schmidt, Jens; Remane, Yvonne; Camu, William; Friede, Tim; Benatar, Michael; Weber, Markus und Lingor, Paul
(2024):
Safety, tolerability, and efficacy of fasudil in amyotrophic lateral sclerosis (ROCK-ALS). A phase 2, randomised, double-blind, placebo-controlled trial.
In: Lancet Neurology, Bd. 23, Nr. 11: S. 1133-1146
[PDF, 849kB]
ORCID: https://orcid.org/0000-0001-6116-6790; Neuwirth, Christoph; Wuu, Joanne; Ludolph, Albert C; Schmidt, Jens; Remane, Yvonne; Camu, William; Friede, Tim; Benatar, Michael; Weber, Markus und Lingor, Paul
(2024):
Safety, tolerability, and efficacy of fasudil in amyotrophic lateral sclerosis (ROCK-ALS). A phase 2, randomised, double-blind, placebo-controlled trial.
In: Lancet Neurology, Bd. 23, Nr. 11: S. 1133-1146
[PDF, 849kB]
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]
Lill, Christina M.; Schjeide, Brit-Maren M.; Graetz, Christiane; Liu, Tian; Damotte, Vincent; Akkad, Denis A.; Blaschke, Paul; Gerdes, Lisa-Ann; Kroner, Antje; Luessi, Felix; Cournu-Rebeix, Isabelle; Hoffjan, Sabine; Winkelmann, Alexander; Touze, Emmanuel; Pico, Fernando; Corcia, Philippe; Otaegui, David; Antigueedad, Alfredo; Alcina, Antonio; Comabella, Manuel; Montalban, Xavier; Olascoaga, Javier; Matesanz, Fuencisla; Dörner, Thomas; Li, Shu-Chen; Steinhagen-Thiessen, Elisabeth; Lindenberger, Ulman; Chan, Andrew; Rieckmann, Peter; Hartung, Hans-Peter; Aktas, Orhan; Lohse, Peter; Buttmann, Mathias; Kümpfel, Tania; Kubisch, Christian; Zettl, Uwe K.; Epplen, Joerg T.; Fontaine, Bertrand; Zipp, Frauke; Vandenbroeck, Koen und Bertram, Lars
(März 2013):
Genome-wide significant association of ANKRD55 rs6859219 and multiple sclerosis risk.
In: Journal of Medical Genetics, Bd. 50, Nr. 3: S. 140-143
[PDF, 127kB]
Lill, Christina M.; Liu, Tian; Schjeide, Brit-Maren M.; Roehr, Johannes T.; Akkad, Denis A.; Damotte, Vincent; Alcina, Antonio; Ortiz, Miguel A.; Arroyo, Rafa; Lopez de Lapuente, Aitzkoa; Blaschke, Paul; Winkelmann, Alexander; Gerdes, Lisa-Ann; Luessi, Felix; Fernadez, Oscar; Izquierdo, Guillermo; Antigüedad, Alfredo; Hoffjan, Sabine; Cournu-Rebeix, Isabelle; Gromöller, Silvana; Faber, Hans; Liebsch, Maria; Meissner, Esther; Chanvillard, Coralie; Touze, Emmanuel; Pico, Fernando; Corcia, Philippe; Dörner, Thomas; Steinhagen-Thiessen, Elisabeth; Baeckman, Lars; Heekeren, Hauke R.; Li, Shu-Chen; Lindenberger, Ulman; Chan, Andrew; Hartung, Hans-Peter; Aktas, Orhan; Lohse, Peter; Kümpfel, Tania; Kubisch, Christian; Epplen, Jörg T.; Zettl, Uwe K.; Fontaine, Bertrand; Vandenbroeck, Koen; Matesanz, Fuencisla; Urcelay, Elena; Bertram, Lars und Zipp, Frauke
(September 2012):
Closing the case of APOE in multiple sclerosis: no association with disease risk in over 29 000 subjects.
In: Journal of medical genetics, Bd. 49, Nr. 9: S. 558-562
[PDF, 217kB]