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Emmanuel Roze

Showing results (301-310 of 332) with videos related to

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The Journal of Clinical Investigation|September 26, 2017
Mutations in the netrin-1 gene cause congenital mirror movementsAurélie Méneret, Elizabeth A Franz, Oriane Trouillard, et al.
Movement Disorders Clinical Practice|February 11, 2022
Current Guidelines for Classifying and Diagnosing Cervical Dystonia: Empirical Evidence and RecommendationsGamze Kilic-Berkmen, Sarah Pirio Richardson, Joel S Perlmutter, et al.
Human Mutation|October 26, 2017
DCC mutation update: Congenital mirror movements, isolated agenesis of the corpus callosum, and developmental split brain syndromeAshley P L Marsh, Timothy J Edwards, Charles Galea, et al.
Neurology|May 9, 2014
Congenital mirror movements: mutational analysis of RAD51 and DCC in 26 casesAurélie Méneret, Christel Depienne, Florence Riant, et al.
Neurology|November 16, 2021
Dopaminergic Therapy for Motor Symptoms in Early Parkinson Disease Practice Guideline Summary: A Report of the AAN Guideline SubcommitteeTamara Pringsheim, Gregory S Day, Don B Smith, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|July 2, 2026
Gene Therapy for Amino Acid Decarboxylase Deficiency: Clinical and Imaging Outcomes in a French CohortClément Dunoyer, Gaëtan Poulen, Marie-Céline François-Heude, et al.
Annals of Neurology|October 13, 2020
Characterization of Recessive Parkinson Disease in a Large Multicenter StudySuzanne Lesage, Ariane Lunati, Marion Houot, et al.
Annals of Neurology|April 24, 2012
Sepiapterin reductase deficiency: a treatable mimic of cerebral palsyJennifer Friedman, Emmanuel Roze, Jose E Abdenur, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|November 17, 2020
Fosmetpantotenate Randomized Controlled Trial in Pantothenate Kinase-Associated NeurodegenerationThomas Klopstock, Aleksandar Videnovic, Almut Turid Bischoff, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|May 1, 2026
Distinct Brain Drivers and Shared Cerebello-Cortical Input in ADCY5 and SGCE Hyperkinetic MovementsClément Tarrano, Cécile Galléa, Asya Ekmen, et al.
Pageof 34

Showing results (301-310 of 332) with videos related to

Sort By:
Pageof 34
The Journal of Clinical Investigation|September 26, 2017
Mutations in the netrin-1 gene cause congenital mirror movementsAurélie Méneret, Elizabeth A Franz, Oriane Trouillard, et al.
Movement Disorders Clinical Practice|February 11, 2022
Current Guidelines for Classifying and Diagnosing Cervical Dystonia: Empirical Evidence and RecommendationsGamze Kilic-Berkmen, Sarah Pirio Richardson, Joel S Perlmutter, et al.
Human Mutation|October 26, 2017
DCC mutation update: Congenital mirror movements, isolated agenesis of the corpus callosum, and developmental split brain syndromeAshley P L Marsh, Timothy J Edwards, Charles Galea, et al.
Neurology|May 9, 2014
Congenital mirror movements: mutational analysis of RAD51 and DCC in 26 casesAurélie Méneret, Christel Depienne, Florence Riant, et al.
Neurology|November 16, 2021
Dopaminergic Therapy for Motor Symptoms in Early Parkinson Disease Practice Guideline Summary: A Report of the AAN Guideline SubcommitteeTamara Pringsheim, Gregory S Day, Don B Smith, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|July 2, 2026
Gene Therapy for Amino Acid Decarboxylase Deficiency: Clinical and Imaging Outcomes in a French CohortClément Dunoyer, Gaëtan Poulen, Marie-Céline François-Heude, et al.
Annals of Neurology|October 13, 2020
Characterization of Recessive Parkinson Disease in a Large Multicenter StudySuzanne Lesage, Ariane Lunati, Marion Houot, et al.
Annals of Neurology|April 24, 2012
Sepiapterin reductase deficiency: a treatable mimic of cerebral palsyJennifer Friedman, Emmanuel Roze, Jose E Abdenur, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|November 17, 2020
Fosmetpantotenate Randomized Controlled Trial in Pantothenate Kinase-Associated NeurodegenerationThomas Klopstock, Aleksandar Videnovic, Almut Turid Bischoff, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|May 1, 2026
Distinct Brain Drivers and Shared Cerebello-Cortical Input in ADCY5 and SGCE Hyperkinetic MovementsClément Tarrano, Cécile Galléa, Asya Ekmen, et al.
Pageof 34