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Emmanuel Roze

Showing results (251-260 of 332) with videos related to

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Journal of Neurology, Neurosurgery, and Psychiatry|February 10, 2021
Quality of life in isolated dystonia: non-motor manifestations matterJohanna Junker, Brian D Berman, James Hall, et al.
Parkinsonism & Related Disorders|May 24, 2025
A delphi consensus statement about French practical management of continuous apomorphine infusion in patients with Parkinson's disease and motor fluctuationsFabienne Ory Magne, Sophie Drapier, Ana-Raquel Marques, et al.
Science Translational Medicine|May 4, 2021
COVID-19-related anosmia is associated with viral persistence and inflammation in human olfactory epithelium and brain infection in hamstersGuilherme Dias de Melo, Françoise Lazarini, Sylvain Levallois, et al.
Neurology|June 30, 2012
PRRT2 mutations: a major cause of paroxysmal kinesigenic dyskinesia in the European populationAurélie Méneret, David Grabli, Christel Depienne, et al.
European Journal of Neurology|October 6, 2022
Movement disorders in valine métabolism diseases caused by HIBCH and ECHS1 deficienciesMarie-Céline François-Heude, Elise Lebigot, Emmanuel Roze, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|September 5, 2025
Abnormal Connectivity of the Head Neural Integrator in Cervical DystoniaGiuseppe A Zito, Emmanuel Roze, Clément Tarrano, et al.
Neurology|April 28, 2019
Long-term outcome in neuroZika: When biological diagnosis mattersAnnie Lannuzel, Jean-Louis Fergé, Quentin Lobjois, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|October 2, 2019
Visual sensory processing is altered in myoclonus dystoniaClément Tarrano, Nicolas Wattiez, Cécile Delorme, et al.
Brain : a Journal of Neurology|September 24, 2013
RAD51 deficiency disrupts the corticospinal lateralization of motor controlCécile Gallea, Traian Popa, Cécile Hubsch, et al.
Orphanet Journal of Rare Diseases|October 5, 2018
Adult Niemann-Pick disease type C in France: clinical phenotypes and long-term miglustat treatment effectYann Nadjar, Ana Lucia Hütter-Moncada, Philippe Latour, et al.
Pageof 34

Showing results (251-260 of 332) with videos related to

Sort By:
Pageof 34
Journal of Neurology, Neurosurgery, and Psychiatry|February 10, 2021
Quality of life in isolated dystonia: non-motor manifestations matterJohanna Junker, Brian D Berman, James Hall, et al.
Parkinsonism & Related Disorders|May 24, 2025
A delphi consensus statement about French practical management of continuous apomorphine infusion in patients with Parkinson's disease and motor fluctuationsFabienne Ory Magne, Sophie Drapier, Ana-Raquel Marques, et al.
Science Translational Medicine|May 4, 2021
COVID-19-related anosmia is associated with viral persistence and inflammation in human olfactory epithelium and brain infection in hamstersGuilherme Dias de Melo, Françoise Lazarini, Sylvain Levallois, et al.
Neurology|June 30, 2012
PRRT2 mutations: a major cause of paroxysmal kinesigenic dyskinesia in the European populationAurélie Méneret, David Grabli, Christel Depienne, et al.
European Journal of Neurology|October 6, 2022
Movement disorders in valine métabolism diseases caused by HIBCH and ECHS1 deficienciesMarie-Céline François-Heude, Elise Lebigot, Emmanuel Roze, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|September 5, 2025
Abnormal Connectivity of the Head Neural Integrator in Cervical DystoniaGiuseppe A Zito, Emmanuel Roze, Clément Tarrano, et al.
Neurology|April 28, 2019
Long-term outcome in neuroZika: When biological diagnosis mattersAnnie Lannuzel, Jean-Louis Fergé, Quentin Lobjois, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|October 2, 2019
Visual sensory processing is altered in myoclonus dystoniaClément Tarrano, Nicolas Wattiez, Cécile Delorme, et al.
Brain : a Journal of Neurology|September 24, 2013
RAD51 deficiency disrupts the corticospinal lateralization of motor controlCécile Gallea, Traian Popa, Cécile Hubsch, et al.
Orphanet Journal of Rare Diseases|October 5, 2018
Adult Niemann-Pick disease type C in France: clinical phenotypes and long-term miglustat treatment effectYann Nadjar, Ana Lucia Hütter-Moncada, Philippe Latour, et al.
Pageof 34