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European Journal of Epidemiology|September 13, 2022
Spatio-temporal clustering of amyotrophic lateral sclerosis in France: A population-based studyFarid Boumédiene, Benoît Marin, Jaime Luna, et al.
Neurology|February 26, 2025
Comparative Performances of 4 Serum NfL Assays, pTau181, and GFAP in Patients With Amyotrophic Lateral SclerosisEtienne Mondesert, Constance Delaby, Elisa De La Cruz, et al.
Frontiers in Neuroscience|May 16, 2020
Clinical Phenotype and Inheritance in Patients With C9ORF72 Hexanucleotide Repeat Expansion: Results From a Large French CohortFlorence Esselin, Kevin Mouzat, Anne Polge, et al.
Clinical Genetics|July 26, 2022
HINT1 neuropathy: Expanding the genotype and phenotype spectrumVictor Morel, Emmanuelle Campana-Salort, Amandine Boyer, et al.
European Journal of Neurology|November 11, 2022
Immune-mediated diseases involving central and peripheral nervous systemsAurelie Leboyan, Florence Esselin, Anne-Laure Bascou, et al.
Amyloid : the International Journal of Experimental and Clinical Investigation : the Official Journal of the International Society of Amyloidosis|October 19, 2023
Hereditary transthyretin amyloidosis in middle-aged and elderly patients with idiopathic polyneuropathy: a nationwide prospective studyGuillaume Fargeot, Andoni Echaniz-Laguna, Céline Labeyrie, et al.
Neurobiology of Disease|July 13, 2024
Caffeine consumption outcomes on amyotrophic lateral sclerosis disease progression and cognitionVincent Huin, David Blum, Violette Delforge, et al.
Mayo Clinic Proceedings. Innovations, Quality & Outcomes|August 4, 2026
Tofersen Treatment in SOD1-ALS: Real-World Evidence from a Retrospective Multicenter Study in France (FORSLA Study)Daniells Erazo, Adele Hesters, Gaëlle Bruneteau, et al.
Acta Neuropathologica Communications|July 3, 2026
Phenotype-specific muscle proteomic profiling in titinopathiesAurélien Perrin, Marie-Rocio Casenave-Camgaston, Baptiste Rabillard, et al.
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