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Neurotherapeutics : the Journal of the American Society for Experimental Neurotherapeutics|March 17, 2012
Alternative approaches to modeling hereditary dystoniasRachel Fremont, Kamran Khodakhah
Movement Disorders : Official Journal of the Movement Disorder Society|August 27, 2017
It's not just the basal ganglia: Cerebellum as a target for dystonia therapeuticsAmbika Tewari, Rachel Fremont, Kamran Khodakhah
Neurobiology of Disease|June 21, 2015
Aberrant Purkinje cell activity is the cause of dystonia in a shRNA-based mouse model of Rapid Onset Dystonia-ParkinsonismRachel Fremont, Ambika Tewari, Kamran Khodakhah
Elife|February 16, 2017
A role for cerebellum in the hereditary dystonia DYT1Rachel Fremont, Ambika Tewari, Chantal Angueyra, et al.
Focus (American Psychiatric Publishing)|July 5, 2023
Ketamine for Treatment of Posttraumatic Stress Disorder: State of the FieldRachel Fremont, Oneysha Brown, Adriana Feder, et al.
Nature Neuroscience|February 8, 2011
The neural substrates of rapid-onset Dystonia-ParkinsonismD Paola Calderon, Rachel Fremont, Franca Kraenzlin, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|August 29, 2014
Abnormal high-frequency burst firing of cerebellar neurons in rapid-onset dystonia-parkinsonismRachel Fremont, D Paola Calderon, Sara Maleki, et al.
Nature Neuroscience|November 18, 2014
Short latency cerebellar modulation of the basal gangliaChristopher H Chen, Rachel Fremont, Eduardo E Arteaga-Bracho, et al.
Elife|December 24, 2019
Acute cerebellar knockdown of Sgce reproduces salient features of myoclonus-dystonia (DYT11) in miceSamantha Washburn, Rachel Fremont, Maria Camila Moreno-Escobar, et al.
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