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Revue Neurologique|May 6, 2014
Pathophysiogical and therapeutic progress in Friedreich ataxiaH Puccio, M Anheim, C TranchantRevue Neurologique|January 4, 2011
[Peripheral neuropathies associated with hereditary cerebellar ataxias]M Anheim, C TranchantRevue Neurologique|February 1, 2006
[Pure trigeminal motor neuropathy presenting with temporo-mandibular joint dysfunction in a patient with HIV and HCV infections]M Anheim, A Echaniz-Laguna, D Rey, et al.Revue Neurologique|September 30, 2004
[Acute relapse in Charcot-Marie-Tooth 1B neuropathy: can protein P0 behave like an autoantigen?]M Fleury, M Anheim, C Tranchant, et al.Neurology|April 27, 2005
A family with early-onset and rapidly progressive X-linked spinal and bulbar muscular atrophyA Echaniz-Laguna, E Rousso, M Anheim, et al.Revue Neurologique|June 1, 2005
[A clinical, neurophysiological and molecular study of 12 patients from 4 families with spinal and bulbar muscular atrophy]A Echaniz-Laguna, E Rousso, M Anheim, et al.Revue Neurologique|March 7, 2006
[Ataxia associated with gluten sensitivity, myth or reality?]M Anheim, B Degos, A Echaniz-Laguna, et al.Revue Neurologique|June 17, 2008
[Severe generalized dystonia due to postradiotherapy cerebral calcifications]J-B Chanson, M Anheim, O Lagha-Boukbiza, et al.Revue Neurologique|December 17, 2004
[Hereditary neuropathy with liability to pressure palsy presenting with an acute inflammatory demyelinating polyneuropathy]B Degos, A Echaniz-Laguna, P Latour, et al.Pageof 17