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Berit Jordan

Showing results (21-30 of 25) with videos related to

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European Journal of Neurology|October 20, 2021
Neurological autoimmune diseases following vaccinations against SARS-CoV-2: a case seriesLeon D Kaulen, Sofia Doubrovinskaia, Christoph Mooshage, et al.
Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration|February 1, 2018
Provision of assistive technology devices among people with ALS in Germany: a platform-case management approachAndreas Funke, Susanne Spittel, Torsten Grehl, et al.
Journal of Clinical Neuroscience : Official Journal of the Neurosurgical Society of Australasia|November 21, 2023
Efficacy and safety of iscalimab, a novel anti-CD40 monoclonal antibody, in moderate-to-severe myasthenia gravis: A phase 2 randomized studyBaltazar GomezMancilla, Matthew N Meriggioli, Angela Genge, et al.
Brain : a Journal of Neurology|January 18, 2021
Bi-allelic truncating mutations in VWA1 cause neuromyopathyMarcus Deschauer, Holger Hengel, Katrin Rupprich, et al.
Brain : a Journal of Neurology|January 18, 2018
Hot-spot KIF5A mutations cause familial ALSDavid Brenner, Rüstem Yilmaz, Kathrin Müller, et al.
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Showing results (21-30 of 25) with videos related to

Sort By:
Pageof 3
You have reached the last page of results.This site can display upto 25 results.
European Journal of Neurology|October 20, 2021
Neurological autoimmune diseases following vaccinations against SARS-CoV-2: a case seriesLeon D Kaulen, Sofia Doubrovinskaia, Christoph Mooshage, et al.
Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration|February 1, 2018
Provision of assistive technology devices among people with ALS in Germany: a platform-case management approachAndreas Funke, Susanne Spittel, Torsten Grehl, et al.
Journal of Clinical Neuroscience : Official Journal of the Neurosurgical Society of Australasia|November 21, 2023
Efficacy and safety of iscalimab, a novel anti-CD40 monoclonal antibody, in moderate-to-severe myasthenia gravis: A phase 2 randomized studyBaltazar GomezMancilla, Matthew N Meriggioli, Angela Genge, et al.
Brain : a Journal of Neurology|January 18, 2021
Bi-allelic truncating mutations in VWA1 cause neuromyopathyMarcus Deschauer, Holger Hengel, Katrin Rupprich, et al.
Brain : a Journal of Neurology|January 18, 2018
Hot-spot KIF5A mutations cause familial ALSDavid Brenner, Rüstem Yilmaz, Kathrin Müller, et al.
Pageof 3