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Journal of Neurology, Neurosurgery, and Psychiatry|April 14, 2018
Comprehensive analysis of the mutation spectrum in 301 German ALS familiesKathrin Müller, David Brenner, Patrick Weydt, et al.Brain Communications|November 3, 2025
Deep clinical, genetic, and serum biomarker profiling indicates glial and neuronal pathology in primary brain calcificationJanine Schwahn, Sophie Hebestreit, Olivia Kosche, et al.The Journal of Experimental Medicine|March 22, 2024
A TBK1 variant causes autophagolysosomal and motoneuron pathology without neuroinflammation in miceDavid Brenner, Kirsten Sieverding, Jahnavi Srinidhi, et al.Acta Neuropathologica Communications|June 26, 2026
A rare missense variant impacting NEK1 kinase function is associated with ALSDavid Brenner, Anna Ponomarenko, Iris Petrut, et al.Brain Communications|May 24, 2023
Spectrum and frequency of genetic variants in sporadic amyotrophic lateral sclerosisWolfgang P Ruf, Matej Boros, Axel Freischmidt, et al.Annals of Neurology|August 9, 2025
Targeted Proteomics upon Treatment with Tofersen Identifies Novel Response Markers for Superoxide Dismutase 1-Linked Amyotrophic Lateral SclerosisChristina Steffke, Karthik Baskar, Franziska Bachhuber, et al.Medrxiv : the Preprint Server for Health Sciences|May 19, 2025
Single cell multiomics reveals drivers of metabolic dysfunction-associated steatohepatitisWeston Elison, Lei Chang, Yang Xie, et al.Brain : a Journal of Neurology|January 18, 2018
Hot-spot KIF5A mutations cause familial ALSDavid Brenner, Rüstem Yilmaz, Kathrin Müller, et al.Life Sciences in Space Research|November 6, 2022
Looking on the horizon; potential and unique approaches to developing radiation countermeasures for deep space travelRihana S Bokhari, Afshin Beheshti, Sarah E Blutt, et al.Eclinicalmedicine|February 22, 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 programMaximilian Wiesenfarth, Johannes Dorst, David Brenner, et al.Pageof 18