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Scientific Reports|June 2, 2017
Mutation Spectrum in the CACNA1A Gene in 49 Patients with Episodic AtaxiaCèlia Sintas, Oriel Carreño, Noèlia Fernàndez-Castillo, et al.Journal of Neuropathology and Experimental Neurology|December 24, 2008
Early-onset familial lewy body dementia with extensive tauopathy: a clinical, genetic, and neuropathological studyJordi Clarimón, Laura Molina-Porcel, Teresa Gómez-Isla, et al.JAMA Neurology|May 24, 2013
New subtype of spinocerebellar ataxia with altered vertical eye movements mapping to chromosome 1p32Carmen Serrano-Munuera, Marc Corral-Juan, Giovanni Stevanin, et al.Journal of Neurology|March 2, 2025
Late-onset vestibulocerebellar ataxia: clinical and genetic studies in a long follow-up series of 50 patientsDavid Genís, Berta Alemany, David Pellerin, et al.Pageof 2