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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.
Neuromuscular Disorders : NMD|October 16, 2004
Myositis in infiltrative lymphocytosis syndrome: clinicopathological observations and treatmentS Attarian, C Mallecourt, A Donnet, et al.
Revue Neurologique|December 22, 1999
[Epilepsy in an adult with chromosome 22q11 micro-deletion]P Alla, N Philip, J P Azulay, et al.
Revue Neurologique|October 10, 2006
[Stiff man syndrome: clinical forms, treatment and clinical course]S Cantiniaux, J P Azulay, J Boucraut, et al.
Revue Neurologique|February 24, 2004
[Chorea-acanthocytosis: report of a new family]D Uzenot, J-P Azulay, S Attarian, et al.
Clinical Neurophysiology : Official Journal of the International Federation of Clinical Neurophysiology|December 14, 2004
Transcranial magnetic stimulation in lower motor neuron diseasesS Attarian, J-Ph Azulay, D Lardillier, et al.
Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology|June 9, 2005
Neuromuscular diseases associated with antigliadin antibodies. A contentious conceptJ Serratrice, S Attarian, P Disdier, et al.
Clinical Neurophysiology : Official Journal of the International Federation of Clinical Neurophysiology|February 24, 2007
Assessment of cortico-spinal tract impairment in multiple system atrophy using transcranial magnetic stimulationA Eusebio, J-P Azulay, T Witjas, 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.
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