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Annals of Clinical and Translational Neurology|October 21, 2020
Multimodal evaluation of an Italian family with a hereditary spastic paraplegia and POLR3A mutationsLucia Ruggiero, Aniello Iovino, Raffaele Dubbioso, et al.Journal of Neurology|March 13, 2022
A compound score to screen patients with hereditary transthyretin amyloidosisStefano Tozza, Daniele Severi, Emanuele Spina, et al.Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|October 23, 2023
Heterogenous electrophysiological features in early stage of hereditary transthyretin amyloidosis neuropathyStefano Tozza, Giovanni Palumbo, Daniele Severi, et al.Antioxidants (Basel, Switzerland)|December 24, 2021
Superoxide Dismutase-1 Intracellular Content in T Lymphocytes Associates with Increased Regulatory T Cell Level in Multiple Sclerosis Subjects Undergoing Immune-Modulating TreatmentValentina Rubino, Anna Teresa Palatucci, Giuliana La Rosa, et al.Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|November 28, 2019
Different cortical excitability profiles in hereditary brain iron and copper accumulationRaffaele Dubbioso, Lucia Ruggiero, Marcello Esposito, et al.Journal of Clinical Medicine|December 19, 2020
Prevalence of SARS-CoV-2 Antibodies in Multiple Sclerosis: The Hidden Part of the IcebergNicola Capasso, Raffaele Palladino, Emma Montella, et al.Epilepsia Open|February 27, 2025
Efficacy and tolerability of low versus standard daily doses of antiseizure medications in newly diagnosed focal epilepsy. A multicenter, randomized, single-blind, non-inferiority trial (STANDLOW)Giorgia Giussani, Elisa Bianchi, Edoardo Carlando, et al.Pageof 2