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European Journal of Neurology|August 7, 2024
Bulbar muscle impairment in patients with late onset Pompe disease: Insight from the French Pompe registryEmilie Retailleau, Claire Lefeuvre, Marie De Antonio, et al.Journal of Neurology|March 2, 2026
Electrophysiological assessment of motor unit loss in adult spinal muscular atrophy types III and IV: a multicenter national study comparing MUNIX, CMAP, and MUSIXEva Sole-Cruz, Emmanuelle Salort-Campana, Timothee Lenglet, et al.Orphanet Journal of Rare Diseases|December 20, 2024
Spinal muscular atrophy is also a disorder of spermatogenesisArmelle Magot, Arnaud Reignier, Olivier Binois, et al.Journal of Neurology|May 20, 2024
Clinical, paraclinical and outcome features of 166 patients with acute anti-GQ1b antibody syndromeMartin Coly, David Adams, Shahram Attarian, et al.Brain : a Journal of Neurology|April 21, 2021
Antibodies to the Caspr1/contactin-1 complex in chronic inflammatory demyelinating polyradiculoneuropathyElba Pascual-Goñi, Janev Fehmi, Cinta Lleixà, et al.Journal of Neurology|July 18, 2020
Antibodies against the node of Ranvier: a real-life evaluation of incidence, clinical features and response to treatment based on a prospective analysis of 1500 seraEmilien Delmont, Alexandre Brodovitch, Ludivine Kouton, et al.European Journal of Neurology|August 1, 2025
Nationwide Phenotypic and Genotypic Characterisation of 103 Patients With SH3TC2 Gene-Related Demyelinating Peripheral NeuropathyPauline Jaubert, Camille Loret, Tanya Stojkovic, et al.Medrxiv : the Preprint Server for Health Sciences|April 10, 2026
High risk of hypoxemic COVID-19 pneumonia in myasthenia gravis patients with type I IFN autoantibodiesAdrian Gervais, Astrid Marchal, Alexis Maillard, et al.Pageof 10