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E Roze

Showing results (41-50 of 51) with videos related to

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Neuroimage. Clinical|June 25, 2015
Increased cortico-striatal connectivity during motor practice contributes to the consolidation of motor memory in writer's cramp patientsC Gallea, M Balas, E Bertasi, et al.
Neurology|April 15, 2009
Propriospinal myoclonus revisited: Clinical, neurophysiologic, and neuroradiologic findingsE Roze, P Bounolleau, D Ducreux, et al.
Neurology|January 19, 2011
A novel DCC mutation and genetic heterogeneity in congenital mirror movementsC Depienne, M Cincotta, S Billot, et al.
Revue Neurologique|April 22, 2014
Solitary tuberculous brain lesions: 24 new cases and a review of the literatureD Psimaras, C Bonnet, A Heinzmann, et al.
Journal of Cosmetic Dermatology|July 6, 2023
SAMCEP Society consensus on the treatment of upper facial lines with botulinum neurotoxin type A: A tailored approachF Braccini, I Catoni, F Belfkira, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|February 5, 2008
The adolescent and adult form of cobalamin C disease: clinical and molecular spectrumC Thauvin-Robinet, E Roze, G Couvreur, et al.
Revue Neurologique|December 27, 2025
Deep brain stimulation in patients with mixed movement disorders linked to ADCY5E Retailleau, N Dorison, G Poulen, et al.
Revue Neurologique|February 5, 2017
"De-novo" consultation: Evaluation of an outpatient's clinic dedicated to early diagnosis of parkinsonian syndromesJ Ruggeri, L-L Mariani, S Aix, et al.
Journal of Medical Genetics|October 18, 2005
Epsilon sarcoglycan mutations and phenotype in French patients with myoclonic syndromesS Tezenas du Montcel, F Clot, M Vidailhet, et al.
Neurology|March 26, 2008
Myoclonus-dystonia: clinical and electrophysiologic pattern related to SGCE mutationsE Roze, E Apartis, F Clot, et al.
Pageof 6

Showing results (41-50 of 51) with videos related to

Sort By:
Pageof 6
Neuroimage. Clinical|June 25, 2015
Increased cortico-striatal connectivity during motor practice contributes to the consolidation of motor memory in writer's cramp patientsC Gallea, M Balas, E Bertasi, et al.
Neurology|April 15, 2009
Propriospinal myoclonus revisited: Clinical, neurophysiologic, and neuroradiologic findingsE Roze, P Bounolleau, D Ducreux, et al.
Neurology|January 19, 2011
A novel DCC mutation and genetic heterogeneity in congenital mirror movementsC Depienne, M Cincotta, S Billot, et al.
Revue Neurologique|April 22, 2014
Solitary tuberculous brain lesions: 24 new cases and a review of the literatureD Psimaras, C Bonnet, A Heinzmann, et al.
Journal of Cosmetic Dermatology|July 6, 2023
SAMCEP Society consensus on the treatment of upper facial lines with botulinum neurotoxin type A: A tailored approachF Braccini, I Catoni, F Belfkira, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|February 5, 2008
The adolescent and adult form of cobalamin C disease: clinical and molecular spectrumC Thauvin-Robinet, E Roze, G Couvreur, et al.
Revue Neurologique|December 27, 2025
Deep brain stimulation in patients with mixed movement disorders linked to ADCY5E Retailleau, N Dorison, G Poulen, et al.
Revue Neurologique|February 5, 2017
"De-novo" consultation: Evaluation of an outpatient's clinic dedicated to early diagnosis of parkinsonian syndromesJ Ruggeri, L-L Mariani, S Aix, et al.
Journal of Medical Genetics|October 18, 2005
Epsilon sarcoglycan mutations and phenotype in French patients with myoclonic syndromesS Tezenas du Montcel, F Clot, M Vidailhet, et al.
Neurology|March 26, 2008
Myoclonus-dystonia: clinical and electrophysiologic pattern related to SGCE mutationsE Roze, E Apartis, F Clot, et al.
Pageof 6