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Cortex; a Journal Devoted to the Study of the Nervous System and Behavior|October 30, 2021
Primary progressive aphasias associated with C9orf72 expansions: Another side of the storyDario Saracino, Amandine Géraudie, Anne M Remes, et al.Neurology|August 8, 2014
Contribution of ATXN2 intermediary polyQ expansions in a spectrum of neurodegenerative disordersSerena Lattante, Stéphanie Millecamps, Giovanni Stevanin, et al.Neurobiology of Aging|July 19, 2017
Novel UBQLN2 mutations linked to amyotrophic lateral sclerosis and atypical hereditary spastic paraplegia phenotype through defective HSP70-mediated proteolysisElisa Teyssou, Laura Chartier, Maria-Del-Mar Amador, et al.European Journal of Neurology|March 12, 2024
European Academy of Neurology (EAN) guideline on the management of amyotrophic lateral sclerosis in collaboration with European Reference Network for Neuromuscular Diseases (ERN EURO-NMD)Philip Van Damme, Ammar Al-Chalabi, Peter M Andersen, et al.Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration|August 30, 2021
Clinical management and disease-modifying treatment for amyotrophic lateral sclerosis in African hospital centers: the TROPALS studyJaime Luna, Jeremy Jost, Mouhamadou Diagana, et al.Journal of Neurology, Neurosurgery, and Psychiatry|September 23, 2018
Clinical features and prognosis of amyotrophic lateral sclerosis in Africa: the TROPALS studyJaime Luna, Mouhamadou Diagana, Leila Ait Aissa, et al.Frontiers in Neurology|October 4, 2018
Structural, Microstructural, and Metabolic Alterations in Primary Progressive Aphasia VariantsAlexandre Routier, Marie-Odile Habert, Anne Bertrand, et al.Movement Disorders : Official Journal of the Movement Disorder Society|April 1, 2021
Fluoxetine for the Symptomatic Treatment of Multiple System Atrophy: The MSA-FLUO TrialOlivier Rascol, Valérie Cochen de Cock, Anne Pavy-Le Traon, et al.Journal of Neurology, Neurosurgery, and Psychiatry|August 5, 2021
Plasma NfL levels and longitudinal change rates in <i>C9orf72</i> and <i>GRN</i>-associated diseases: from tailored references to clinical applicationsDario Saracino, Karim Dorgham, Agnès Camuzat, et al.Journal of Medical Genetics|June 26, 2010
SOD1, ANG, VAPB, TARDBP, and FUS mutations in familial amyotrophic lateral sclerosis: genotype-phenotype correlationsStéphanie Millecamps, François Salachas, Cécile Cazeneuve, et al.Pageof 13