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Emmanuel Roze

Showing results (281-290 of 332) with videos related to

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Brain : a Journal of Neurology|June 4, 2009
Exhaustive analysis of BH4 and dopamine biosynthesis genes in patients with Dopa-responsive dystoniaFabienne Clot, David Grabli, Cécile Cazeneuve, et al.
Brain : a Journal of Neurology|December 21, 2023
Biallelic BORCS8 variants cause an infantile-onset neurodegenerative disorder with altered lysosome dynamicsRaffaella De Pace, Reza Maroofian, Adeline Paimboeuf, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|August 27, 2020
Clinical and Demographic Characteristics of Upper Limb DystoniaScott A Norris, Hyder A Jinnah, Christine Klein, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|March 12, 2026
Missense Variants in the A Isoform of FGF13 as a Novel Cause of Paroxysmal DyskinesiaCyril Mignot, Matthildi Athina Papathanasiou Terzi, Claudia Ravelli, et al.
Brain Communications|April 11, 2024
Association of abnormal explicit sense of agency with cerebellar impairment in myoclonus-dystoniaClément Tarrano, Cécile Galléa, Cécile Delorme, et al.
Brain : a Journal of Neurology|March 27, 2015
PMPCA mutations cause abnormal mitochondrial protein processing in patients with non-progressive cerebellar ataxiaRebekah K Jobling, Mirna Assoum, Oleksandr Gakh, et al.
American Journal of Human Genetics|February 7, 2012
RAD51 haploinsufficiency causes congenital mirror movements in humansChristel Depienne, Delphine Bouteiller, Aurélie Méneret, et al.
Scientific Reports|August 20, 2020
Dissociation in reactive and proactive inhibitory control in Myoclonus dystoniaCyril Atkinson-Clement, Clement Tarrano, Camille-Albane Porte, et al.
Movement Disorders Clinical Practice|May 19, 2023
Transitional Care for Young People with Movement Disorders: Consensus-Based Recommendations from the MDS Task Force on PediatricsTamara Pringsheim, Amit Batla, Ali Shalash, et al.
Orphanet Journal of Rare Diseases|October 30, 2013
Phenotypic variability in ARCA2 and identification of a core ataxic phenotype with slow progressionCyril Mignot, Emmanuelle Apartis, Alexandra Durr, et al.
Pageof 34

Showing results (281-290 of 332) with videos related to

Sort By:
Pageof 34
Brain : a Journal of Neurology|June 4, 2009
Exhaustive analysis of BH4 and dopamine biosynthesis genes in patients with Dopa-responsive dystoniaFabienne Clot, David Grabli, Cécile Cazeneuve, et al.
Brain : a Journal of Neurology|December 21, 2023
Biallelic BORCS8 variants cause an infantile-onset neurodegenerative disorder with altered lysosome dynamicsRaffaella De Pace, Reza Maroofian, Adeline Paimboeuf, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|August 27, 2020
Clinical and Demographic Characteristics of Upper Limb DystoniaScott A Norris, Hyder A Jinnah, Christine Klein, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|March 12, 2026
Missense Variants in the A Isoform of FGF13 as a Novel Cause of Paroxysmal DyskinesiaCyril Mignot, Matthildi Athina Papathanasiou Terzi, Claudia Ravelli, et al.
Brain Communications|April 11, 2024
Association of abnormal explicit sense of agency with cerebellar impairment in myoclonus-dystoniaClément Tarrano, Cécile Galléa, Cécile Delorme, et al.
Brain : a Journal of Neurology|March 27, 2015
PMPCA mutations cause abnormal mitochondrial protein processing in patients with non-progressive cerebellar ataxiaRebekah K Jobling, Mirna Assoum, Oleksandr Gakh, et al.
American Journal of Human Genetics|February 7, 2012
RAD51 haploinsufficiency causes congenital mirror movements in humansChristel Depienne, Delphine Bouteiller, Aurélie Méneret, et al.
Scientific Reports|August 20, 2020
Dissociation in reactive and proactive inhibitory control in Myoclonus dystoniaCyril Atkinson-Clement, Clement Tarrano, Camille-Albane Porte, et al.
Movement Disorders Clinical Practice|May 19, 2023
Transitional Care for Young People with Movement Disorders: Consensus-Based Recommendations from the MDS Task Force on PediatricsTamara Pringsheim, Amit Batla, Ali Shalash, et al.
Orphanet Journal of Rare Diseases|October 30, 2013
Phenotypic variability in ARCA2 and identification of a core ataxic phenotype with slow progressionCyril Mignot, Emmanuelle Apartis, Alexandra Durr, et al.
Pageof 34