Patrick Weydt
Safety, tolerability, and efficacy of fasudil in amyotrophic lateral sclerosis (ROCK-ALS): a phase 2, randomised, double-blind, placebo-controlled trial.
Koch J, Leha A, Bidner H, Cordts I, Dorst J, Günther R, Zeller D, Braun N, Metelmann M, Corcia P, Depla E, Weydt P, Meyer T, Grosskreutz J, Soriani M, Attarian S, Weishaupt J, Weyen U, Kuttler J, Zurek G, Rogers M, Feneberg E, Deschauer M, Neuwirth C, Wuu J, Ludolph A, Schmidt J, Remane Y, Camu W, Friede T, Benatar M, Weber M, Lingor P, ROCK-ALS Study group. Safety, tolerability, and efficacy of fasudil in amyotrophic lateral sclerosis (ROCK-ALS): a phase 2, randomised, double-blind, placebo-controlled trial. Lancet Neurol 2024; 23:1133-1146.
Nov 1, 2024Safety, tolerability, and efficacy of fasudil in amyotrophic lateral sclerosis (ROCK-ALS): a phase 2, randomised, double-blind, placebo-controlled trial.
Nov 1, 2024Lancet Neurol 2024; 23:1133-1146
Koch Jan Christoph, Leha Andreas, Bidner Helen, Cordts Isabell, Dorst Johannes, Günther René, Zeller Daniel, Braun Nathalie, Metelmann Moritz, Corcia Philippe, Depla Erik, 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, Neuwirth Christoph, Wuu Joanne, Ludolph Albert C., Schmidt Jens, Remane Yvonne, Camu William, Friede Tim, Benatar Michael, Weber Markus, Lingor Paul, ROCK-ALS Study group
Reply: Adult-onset distal spinal muscular atrophy: a new phenotype associated with KIF5A mutations
German ALS network MND-NET, Weis J, Dorst J, Volk A, Borck G, Sperfeld A, de Carvalho M, Klopstock T, Sendtner M, Otto M, Schuster J, Weishaupt J, Andersen P, Ludolph A, Meitinger T, Freischmidt A, Danzer K, Braak H, Del Tredici K, Jablonka S, Kubisch C, Zeller D, Weydt P, Grosskreutz J, Meyer T, Petri S, Grehl T, Müller K, Yilmaz R, Rosenbohm A, Ruf W, Neuwirth C, Hübers A, Günther K, Knehr A, Jordan B, Schrank B, Claeys K, Pinto S, Weber M, Brenner D. Reply: Adult-onset distal spinal muscular atrophy: a new phenotype associated with KIF5A mutations. Brain 2019; 142:e67.
Jan 1, 2019Reply: Adult-onset distal spinal muscular atrophy: a new phenotype associated with KIF5A mutations
Jan 1, 2019Brain 2019; 142:e67
German ALS network MND-NET, Weis Joachim, Dorst Johannes, Volk Alexander E, Borck Guntram, Sperfeld Anne, de Carvalho Mamede, Klopstock Thomas, Sendtner Michael, Otto Markus, Schuster Joachim, Weishaupt Jochen H, Andersen Peter M, Ludolph Albert C, Meitinger Thomas, Freischmidt Axel, Danzer Karin M, Braak Heiko, Del Tredici Kelly, Jablonka Sibylle, Kubisch Christian, Zeller Daniel, Weydt Patrick, Grosskreutz Julian, Meyer Thomas, Petri Susanne, Grehl Torsten, Müller Kathrin, Yilmaz Rüstem, Rosenbohm Angela, Ruf Wolfgang, Neuwirth Christoph, Hübers Annemarie, Günther Kornelia, Knehr Antje, Jordan Berit, Schrank Berthold, Claeys Kristl G, Pinto Susana, Weber Markus, Brenner David
Hot-spot KIF5A mutations cause familial ALS
Weishaupt J, Weis J, Dorst J, Volk A, Borck G, Sperfeld A, de Carvalho M, Klopstock T, Sendtner M, Otto M, Schuster J, Andersen P, Ludolph A, Strom T, Meitinger T, Freischmidt A, Danzer K, Braak H, Del Tredici K, Jablonka S, Kubisch C, German ALS network MND-NET, Ruf W, Weydt P, Grosskreutz J, Meyer T, Petri S, Grehl T, Müller K, Yilmaz R, Neuwirth C, Weber M, Zeller D, Hübers A, Günther K, Knehr A, Jordan B, Schrank B, Claeys K, Pinto S, Brenner D. Hot-spot KIF5A mutations cause familial ALS. Brain 2018
Jan 12, 2018Hot-spot KIF5A mutations cause familial ALS
Jan 12, 2018Brain 2018
Weishaupt Jochen H, Weis Joachim, Dorst Johannes, Volk Alexander E, Borck Guntram, Sperfeld Anne, de Carvalho Mamede, Klopstock Thomas, Sendtner Michael, Otto Markus, Schuster Joachim, Andersen Peter M, Ludolph Albert C, Strom Tim M, Meitinger Thomas, Freischmidt Axel, Danzer Karin M, Braak Heiko, Del Tredici Kelly, Jablonka Sibylle, Kubisch Christian, German ALS network MND-NET, Ruf Wolfgang, Weydt Patrick, Grosskreutz Julian, Meyer Thomas, Petri Susanne, Grehl Torsten, Müller Kathrin, Yilmaz Rüstem, Neuwirth Christoph, Weber Markus, Zeller Daniel, Hübers Annemarie, Günther Kornelia, Knehr Antje, Jordan Berit, Schrank Berthold, Claeys Kristl G, Pinto Susana, Brenner David
July 2017 ENCALS statement on edaravone
van den Berg L, Silani V, Shaw P, Salachas F, Povedano Panades M, Petri S, Nygren I, Mora Pardina J, Mitre Ropero B, Staaf G, Svenstrup K, Hardiman O, Wolf J, Weydt P, Weber M, van der Kooi A, Van Damme P, Tysnes O, Talbot K, Meyer T, McDermott C, Ludolph A, Desnuelle C, de Carvalho M, Danielsson O, Couratier P, Corcia P, Chio A, Chandran S, Andersen P, Grehl T, Grosskreutz J, Laaksovirta H, KuzmaKozakiewicz M, Koritnik B, Koch J, Kleveland G, Karlsborg M, Ingre C, Holmøy T, Al-Chalabi A. July 2017 ENCALS statement on edaravone. Amyotroph Lateral Scler Frontotemporal Degener 2017; 18:471-474.
Oct 4, 2017July 2017 ENCALS statement on edaravone
Oct 4, 2017Amyotroph Lateral Scler Frontotemporal Degener 2017; 18:471-474
van den Berg Leonard H, Silani Vincenzo, Shaw Pamela, Salachas François, Povedano Panades Mónica, Petri Susanne, Nygren Ingela, Mora Pardina Jesus, Mitre Ropero Bernardo, Staaf Gert, Svenstrup Kirsten, Hardiman Orla, Wolf Joachim, Weydt Patrick, Weber Markus, van der Kooi Anneke, Van Damme Philip, Tysnes Ole-Bjørn, Talbot Kevin, Meyer Thomas, McDermott Christopher, Ludolph Albert, Desnuelle Claude, de Carvalho Mamede, Danielsson Olof, Couratier Philippe, Corcia Philippe, Chio Adriano, Chandran Siddharthan, Andersen Peter M, Grehl Torsten, Grosskreutz Julian, Laaksovirta Hannu, KuzmaKozakiewicz Magdalena, Koritnik Blaž, Koch Jan Christoph, Kleveland Grethe, Karlsborg Merete, Ingre Caroline, Holmøy Trygve, Al-Chalabi Ammar
NEK1 mutations in familial amyotrophic lateral sclerosis
Brenner D, Danzer K, Volk A, Meitinger T, Strom T, Otto M, Kassubek J, Ludolph A, Andersen P, Wahlqvist M, Borck G, Müller K, Wieland T, Weydt P, Böhm S, Lule D, Hübers A, Neuwirth C, Weber M, Weishaupt J. NEK1 mutations in familial amyotrophic lateral sclerosis. Brain 2016
Mar 5, 2016NEK1 mutations in familial amyotrophic lateral sclerosis
Mar 5, 2016Brain 2016
Brenner David, Danzer Karin M, Volk Alexander E, Meitinger Thomas, Strom Tim M, Otto Markus, Kassubek Jan, Ludolph Albert C, Andersen Peter M, Wahlqvist Magnus, Borck Guntram, Müller Kathrin, Wieland Thomas, Weydt Patrick, Böhm Sarah, Lule Dorotheé, Hübers Annemarie, Neuwirth Christoph, Weber Markus, Weishaupt Jochen H
Can lesions to the motor cortex induce amyotrophic lateral sclerosis?
Rosenbohm A, Ludolph A, Weishaupt J, Andersen P, Weber M, Huppertz H, Kubisch C, Volk A, Marroquin N, Weydt P, Kassubek J, ALS Schwaben Register Group. Can lesions to the motor cortex induce amyotrophic lateral sclerosis?. J Neurol 2013; 261:283-90.
Nov 20, 2013Can lesions to the motor cortex induce amyotrophic lateral sclerosis?
Nov 20, 2013J Neurol 2013; 261:283-90
Rosenbohm Angela, Ludolph Albert C, Weishaupt Jochen H, Andersen Peter M, Weber Markus, Huppertz Hans-Jürgen, Kubisch Christian, Volk Alexander E, Marroquin Nicolai, Weydt Patrick, Kassubek Jan, ALS Schwaben Register Group