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Spinocerebellar ataxia type 2: Measures of saccade changes improve power for clinical trials
Authors:Roberto Rodríguez‐Labrada PhD  Luis Velázquez‐Pérez DSc  Georg Auburger MD  Ulf Ziemann MD  Nalia Canales‐Ochoa BSc  Jacqueline Medrano‐Montero PhD  Yaimeé Vázquez‐Mojena MSc  Yanetza González‐Zaldivar BSc
Affiliation:1. Department of Clinical Neurophysiology, Center for the Research and Rehabilitation of Hereditary Ataxias, Holguín, Cuba;2. Section of Experimental Neurology, Department of Neurology, Goethe University Medical School, Frankfurt am Main, Germany;3. Department of Neurology & Stroke, and Hertie Institute for Clinical Brain Research, University Tübingen, Tübingen, Germany;4. Department of Molecular Neurobiology, Center for the Research and Rehabilitation of Hereditary Ataxias, Holguín, Cuba
Abstract:
Keywords:spinocerebellar ataxias  SCA2  saccadic eye movements  saccade slowing  longitudinal study  clinical trials
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