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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.Annals of the Rheumatic Diseases|September 5, 2007
Increased exposure to statins in patients developing chronic muscle diseases: a 2-year retrospective studyL Sailler, C Pereira, A Bagheri, et al.Emerging Infectious Diseases|October 23, 2015
Neurologic Disorders in Immunocompetent Patients with Autochthonous Acute Hepatitis EH Blasco Perrin, P Cintas, F Abravanel, et al.La Revue De Medecine Interne|January 14, 2024
French protocol for the diagnosis and management of hematopoietic stem cell transplantation in autoimmune diseasesD Farge, G Pugnet, M Allez, et al.Revue Neurologique|April 5, 2023
Current clinical management of CIDP with immunoglobulins in France: An expert opinionP Cintas, F Bouhour, C Cauquil, et al.Neuropathology and Applied Neurobiology|April 29, 2020
Novel CAPN3 variant associated with an autosomal dominant calpainopathyM Cerino, E Campana-Salort, A Salvi, 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.Neuromuscular Disorders : NMD|March 7, 2023
A new score combining compound muscle action potential (CMAP) amplitudes and motor score is predictive of motor outcome after AVXS-101 (Onasemnogene Abeparvovec) SMA therapyR Barrois, C Barnerias, E Deladrière, et al.Journal of the Neurological Sciences|October 22, 2019
Implication of the SH3TC2 gene in Charcot-Marie-Tooth disease associated with deafness and/or scoliosis: Illustration with four new pathogenic variantsJ Lerat, C Magdelaine, A Lunati, et al.Neurology|August 6, 2008
Dehydroepiandrosterone for myotonic dystrophy type 1I Pénisson-Besnier, M Devillers, R Porcher, et al.Pageof 5