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BMC Neurology|December 29, 2018
Subclinical Leber's hereditary optic neuropathy with pediatric acute spinal cord onset: more than meets the eyeEleonora Mauri, Robertino Dilena, Antonio Boccazzi, et al.Frontiers in Neurology|December 18, 2018
Central Nervous System Involvement in Common Variable Immunodeficiency: A Case of Acute Unilateral Optic Neuritis in a 26-Year-Old Italian PatientElena Abati, Irene Faravelli, Francesca Magri, et al.Journal of Neuroimmunology|June 28, 2005
E-selectin A561C and G98T polymorphisms influence susceptibility and course of multiple sclerosisDaniela Galimberti, Chiara Fenoglio, Raffaella Clerici, et al.Frontiers in Neurology|September 24, 2021
Sodium Levels Predict Disability at Discharge in Guillain-Barré Syndrome: A Retrospective Cohort StudyDelia Gagliardi, Irene Faravelli, Manuel Alfredo Podestà, et al.Journal of the Neurological Sciences|August 18, 2009
Progranulin plasma levels as potential biomarker for the identification of GRN deletion carriers. A case with atypical onset as clinical amnestic Mild Cognitive Impairment converted to Alzheimer's diseaseMiryam Carecchio, Chiara Fenoglio, Milena De Riz, et al.International Journal of Molecular Sciences|September 9, 2022
Antisense Morpholino-Based In Vitro Correction of a Pseudoexon-Generating Variant in the SGCB GeneFrancesca Magri, Simona Zanotti, Sabrina Salani, et al.Frontiers in Neurology|August 18, 2018
Bilateral Cavernous Carotid Aneurysms: Atypical Presentation of a Rare Cause of Mass Effect. A Case Report and a Review of the LiteratureDelia Gagliardi, Irene Faravelli, Luisa Villa, et al.Scientific Reports|April 7, 2017
Genome-wide RNA-seq of iPSC-derived motor neurons indicates selective cytoskeletal perturbation in Brown-Vialetto disease that is partially rescued by riboflavinFederica Rizzo, Agnese Ramirez, Claudia Compagnucci, et al.Journal of Neurology|June 15, 2006
Follow-up of a large population of asymptomatic/oligosymptomatic hyperckemic subjectsElisabetta D'Adda, Monica Sciacco, Maria Elisa Fruguglietti, et al.Neuroscience Letters|September 11, 2007
Candidate gene analysis of SPARCL1 gene in patients with multiple sclerosisDiego Scalabrini, Chiara Fenoglio, Elio Scarpini, et al.Pageof 34