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Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|December 28, 2020
Clinical features of spinal muscular atrophy (SMA) type 3 (Kugelberg-Welander disease)E Salort-Campana, S Quijano-RoyRevue Neurologique|March 31, 2009
[Seronegative myasthenia and myasthenia gravis with anti-MuSK antibody: a retrospective study of 20 cases]S Aubert, E Salort-Campana, J Franques, et al.Revue Neurologique|July 4, 2007
[Cognitive disorders in multiple sclerosis]B Brochet, M Bonnet, M Deloire, et al.Revue Neurologique|September 10, 2013
[Clinical and molecular diagnosis of facioscapulohumeral dystrophy type 1 (FSHD1) in 2012]E Salort-Campana, K Nguyen, N Lévy, et al.Revue Neurologique|May 4, 2012
Recommendations for the management of facioscapulohumeral muscular dystrophy in 2011S Attarian, E Salort-Campana, K Nguyen, et al.La Revue De Medecine Interne|December 24, 2013
[Necrotizing myopathies: From genetic to acquired forms]E Salort-Campana, A M De Paula, D Figarella-Branger, et al.Revue Neurologique|September 25, 2016
Muscle MRI of facioscapulohumeral dystrophy (FSHD): A growing demand and a promising approachF Fatehi, E Salort-Campana, A Le Troter, et al.Revue Neurologique|November 17, 2018
Guillain-Barré syndrome subtypes: A clinical electrophysiological study of 100 patientsA-M Grapperon, M Berro, E Salort-Campana, et al.Journal of Neurology|October 10, 2024
Treatment of myasthenia gravis in france: A retrospective claims database study (STAMINA)C Tard, P Laforet, G de Pouvourville, et al.Multiple Sclerosis (Houndmills, Basingstoke, England)|August 12, 2006
How to detect cognitive dysfunction at early stages of multiple sclerosis?M S A Deloire, M C Bonnet, E Salort, et al.Pageof 3