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Journal of Neurology, Neurosurgery, and Psychiatry|June 3, 2017
Immunotherapies in neuromyelitis optica spectrum disorder: efficacy and predictors of responseJan-Patrick Stellmann, Markus Krumbholz, Tim Friede, et al.Annals of Neurology|November 6, 2015
Neuromyelitis optica: Evaluation of 871 attacks and 1,153 treatment coursesIngo Kleiter, Anna Gahlen, Nadja Borisow, et al.Multiple Sclerosis (Houndmills, Basingstoke, England)|October 21, 2016
Influence of female sex and fertile age on neuromyelitis optica spectrum disordersNadja Borisow, Ingo Kleiter, Anna Gahlen, et al.Nature Communications|February 14, 2026
Loss-of-function variants in the CAPN1 activator CD99L2 cause X-linked spastic ataxiaBenita Menden, Rana D Incebacak Eltemur, German Demidov, et al.Nature Genetics|July 22, 2024
Next-generation phenotyping integrated in a national framework for patients with ultrarare disorders improves genetic diagnostics and yields new molecular findingsAxel Schmidt, Magdalena Danyel, Kathrin Grundmann, et al.Nature Genetics|May 16, 2025
Dominant variants in major spliceosome U4 and U5 small nuclear RNA genes cause neurodevelopmental disorders through splicing disruptionCaroline Nava, Benjamin Cogne, Amandine Santini, et al.Pageof 2