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Revue Neurologique|May 18, 2010
[Research in amyotrophic lateral sclerosis: what is new in 2009?]P-F Pradat, S Attarian, J-P Camdessanché, et al.Revue Neurologique|May 21, 2026
Primary Lateral Sclerosis French National Diagnostic and Care ProtocolP Corcia, E Bernard, E de la Cruz, et al.European Journal of Neurology|August 2, 2025
Prevalence of SOD1 and C9orf72 Variants Among French ALS Population: The GENIALS StudyP Corcia, D Erazo, M D M Amador, et al.Revue Neurologique|September 7, 2013
The French Pompe registry. Baseline characteristics of a cohort of 126 patients with adult Pompe diseaseP Laforêt, K Laloui, B Granger, et al.European Journal of Neurology|November 1, 2008
Causes of death amongst French patients with amyotrophic lateral sclerosis: a prospective studyJ Gil, B Funalot, A Verschueren, et al.Mitochondrion|December 15, 2007
Rapid identification of mitochondrial DNA (mtDNA) mutations in neuromuscular disorders by using surveyor strategyS Bannwarth, V Procaccio, C Rouzier, et al.Neurology|October 27, 2010
Clinical features of facioscapulohumeral muscular dystrophy 2J C de Greef, R J L F Lemmers, P Camaño, et al.Neurology|December 10, 2008
The CHRNE 1293insG founder mutation is a frequent cause of congenital myasthenia in North AfricaP Richard, K Gaudon, H Haddad, et al.Neurology|August 6, 2008
Dehydroepiandrosterone for myotonic dystrophy type 1I Pénisson-Besnier, M Devillers, R Porcher, et al.Journal of Neurology|November 1, 2023
Quantitative brainstem and spinal MRI in amyotrophic lateral sclerosis: implications for predicting noninvasive ventilation needsM Khamaysa, M Lefort, M Pélégrini-Issac, et al.Pageof 11