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Handbook of Clinical Neurology|August 11, 2011
Spinocerebellar ataxia type 20Elsdon Storey, R J McKinlay GardnerHandbook of Clinical Neurology|August 11, 2011
Spinocerebellar ataxia type 15Elsdon Storey, R J McKinlay GardnerCerebellum (London, England)|May 18, 2005
Spinocerebellar ataxia type 20Elsdon Storey, Melanie A Knight, Susan M Forrest, et al.Cerebellum (London, England)|May 18, 2005
Spinocerebellar ataxia type 15R J McKinlay Gardner, Melanie A Knight, Kenju Hara, et al.Brain : a Journal of Neurology|March 5, 2004
Dominantly inherited ataxia and dysphonia with dentate calcification: spinocerebellar ataxia type 20Melanie A Knight, R J McKinlay Gardner, Melanie Bahlo, et al.Cerebellum (London, England)|September 18, 2015
Non-Ataxic Presenting Symptoms of Dominant AtaxiasElsdon StoreyAmerican Journal of Medical Genetics. Part A|June 11, 2005
Dentatorubral-pallidoluysian atrophy in three generations, with clinical courses from nearly asymptomatic elderly to severe juvenile, in an Australian family of Macedonian descentAnita Vinton, Michael C Fahey, Terence J O'Brien, et al.Brain Sciences|July 15, 2017
Cognitive Changes in the Spinocerebellar Ataxias Due to Expanded Polyglutamine Tracts: A Survey of the LiteratureEvelyn Lindsay, Elsdon StoreyJournal of Clinical Neuroscience : Official Journal of the Neurosurgical Society of Australasia|January 11, 2005
Increased T2 signal in the middle cerebellar peduncles on MRI is not specific for fragile X premutation syndromeElsdon Storey, Phiroz BillimoriaPageof 18