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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.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|January 28, 2003
PARK6 is a common cause of familial parkinsonismE M Valente, F Brancati, V Caputo, et al.
Neurology|January 28, 2004
Clinical and genetic studies in hereditary spastic paraplegia with thin corpus callosumC Casali, E M Valente, E Bertini, et al.
Annals of Neurology|February 16, 1999
Friedreich's ataxia: point mutations and clinical presentation of compound heterozygotesM Cossée, A Dürr, M Schmitt, et al.
Bioorganic & Medicinal Chemistry Letters|August 15, 2015
Discovery of selective N-[3-(1-methyl-piperidine-4-carbonyl)-phenyl]-benzamide-based 5-HT₁ F receptor agonists: Evolution from bicyclic to monocyclic coresDeyi Zhang, Maria-Jesus Blanco, Bai-Ping Ying, et al.
Neurology|February 24, 2010
Responsiveness of different rating instruments in spinocerebellar ataxia patientsT Schmitz-Hübsch, R Fimmers, M Rakowicz, et al.
Neurology|August 13, 2008
SCA Functional Index: a useful compound performance measure for spinocerebellar ataxiaT Schmitz-Hübsch, P Giunti, D A Stephenson, et al.
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