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Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|June 15, 2010
Efficacy and tolerability of natalizumab in relapsing-remitting multiple sclerosis patients: a post-marketing observational studyF Sangalli, L Moiola, S Bucello, et al.Infant Behavior & Development|July 25, 2016
Paths of cognitive and language development in healthy preterm infantsChiara Ionio, Elisa Riboni, Emanuela Confalonieri, et al.Parkinsonism & Related Disorders|July 26, 2016
Cognitive impairment in progressive supranuclear palsy-Richardson's syndrome is related to white matter damageFrancesca Caso, Federica Agosta, Maria Antonietta Volonté, et al.BMC Neurology|June 9, 2011
Computational classifiers for predicting the short-term course of Multiple sclerosisBartolome Bejarano, Mariangela Bianco, Dolores Gonzalez-Moron, et al.Radiology|June 16, 2011
Intrinsic damage to the major white matter tracts in patients with different clinical phenotypes of multiple sclerosis: a voxelwise diffusion-tensor MR studyPaolo Preziosa, Maria A Rocca, Sarlota Mesaros, et al.Journal of Alzheimer'S Disease : JAD|September 25, 2015
Following the Spreading of Brain Structural Changes in Alzheimer's Disease: A Longitudinal, Multimodal MRI StudyMarina Weiler, Federica Agosta, Elisa Canu, et al.Brain Pathology (Zurich, Switzerland)|July 4, 2019
Non-invasive visual evoked potentials to assess optic nerve involvement in the dark agouti rat model of experimental autoimmune encephalomyelitis induced by myelin oligodendrocyte glycoproteinValerio Castoldi, Silvia Marenna, Raffaele d'Isa, et al.European Cytokine Network|December 6, 2003
Serial immunoprecipitation assays for interferon--(IFN)-beta antibodies in multiple sclerosis patientsVito Lampasona, Jordi Rio, Diego Franciotta, et al.Scandinavian Journal of Gastroenterology|December 3, 2016
Anti-sulfatide reactivity in patients with celiac diseaseDomenica Saccomanno, Carolina Tomba, Francesca Magri, et al.Neurology|April 10, 2003
A mitochondrial tRNA(His) gene mutation causing pigmentary retinopathy and neurosensorial deafnessM Crimi, S Galbiati, M P Perini, et al.Pageof 254