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Journal of the Neurological Sciences|May 1, 1999
Consensus statement on the diagnosis of multiple system atrophyS Gilman, P A Low, N Quinn, et al.Journal of the Autonomic Nervous System|January 23, 1999
Consensus statement on the diagnosis of multiple system atrophyS Gilman, P A Low, N Quinn, et al.Human Molecular Genetics|December 1, 1996
Screening for proteins with polyglutamine expansions in autosomal dominant cerebellar ataxiasG Stevanin, Y Trottier, G Cancel, et al.Annals of the New York Academy of Sciences|April 14, 2005
Saccade velocity as a surrogate disease marker in spinocerebellar ataxia type 2C Seifried, L Velázquez-Pérez, N Santos-Falcón, et al.European Neurology|November 14, 2012
Prospective analysis of falls in dominant ataxiasE M R Fonteyn, T Schmitz-Hübsch, C C P Verstappen, et al.Clinical Neurophysiology : Official Journal of the International Federation of Clinical Neurophysiology|February 10, 2009
Saccade velocity is reduced in presymptomatic spinocerebellar ataxia type 2L Velázquez-Pérez, C Seifried, M Abele, et al.Neurology|August 30, 2008
Second consensus statement on the diagnosis of multiple system atrophyS Gilman, G K Wenning, P A Low, et al.Cerebellum (London, England)|October 24, 2012
Inventory of Non-Ataxia Signs (INAS): validation of a new clinical assessment instrumentH Jacobi, M Rakowicz, R Rola, et al.Human Molecular Genetics|May 1, 1997
Molecular and clinical correlations in spinocerebellar ataxia 2: a study of 32 familiesG Cancel, A Dürr, O Didierjean, et al.Neurology|February 24, 2010
Responsiveness of different rating instruments in spinocerebellar ataxia patientsT Schmitz-Hübsch, R Fimmers, M Rakowicz, et al.Pageof 22