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Showing results (41-50 of 49) with videos related to

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Neurology|July 14, 2004
Absence of antibodies to glutamate receptor type 3 (GluR3) in Rasmussen encephalitisR Watson, Y Jiang, I Bermudez, et al.
JIMD Reports|May 17, 2017
Ketone Bodies as a Possible Adjuvant to Ketogenic Diet in PDHc Deficiency but Not in GLUT1 DeficiencyF Habarou, N Bahi-Buisson, E Lebigot, et al.
Revue Neurologique|May 17, 2024
French guidelines for the diagnosis and management of Tourette syndromeA Hartmann, S Ansquer, C Brefel-Courbon, 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.
JIMD Reports|May 6, 2016
Chronic Diarrhea in L-Amino Acid Decarboxylase (AADC) Deficiency: A Prominent Clinical Finding Among a Series of Ten French PatientsM A Spitz, M A Nguyen, S Roche, et al.
Revue Neurologique|June 1, 2025
French guidelines for the diagnosis and management of pure hereditary spastic paraplegiaL Mania-Pâris, C Ewenczyk, G Nicolas, et al.
Journal of Medical Genetics|August 30, 2008
Refinement of cortical dysgeneses spectrum associated with TUBA1A mutationsN Bahi-Buisson, K Poirier, N Boddaert, et al.
Neurogenetics|March 7, 2008
Is the early-onset torsion dystonia (EOTD) linked to TOR1A gene as frequent as expected in France?M Y Frédéric, F Clot, L Cif, et al.
European Journal of Neurology|June 20, 2020
Deciphering the natural history of SCA7 in childrenM G Bah, D Rodriguez, C Cazeneuve, et al.
Pageof 5

Showing results (41-50 of 49) with videos related to

Sort By:
Pageof 5
You have reached the last page of results.This site can display upto 49 results.
Neurology|July 14, 2004
Absence of antibodies to glutamate receptor type 3 (GluR3) in Rasmussen encephalitisR Watson, Y Jiang, I Bermudez, et al.
JIMD Reports|May 17, 2017
Ketone Bodies as a Possible Adjuvant to Ketogenic Diet in PDHc Deficiency but Not in GLUT1 DeficiencyF Habarou, N Bahi-Buisson, E Lebigot, et al.
Revue Neurologique|May 17, 2024
French guidelines for the diagnosis and management of Tourette syndromeA Hartmann, S Ansquer, C Brefel-Courbon, 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.
JIMD Reports|May 6, 2016
Chronic Diarrhea in L-Amino Acid Decarboxylase (AADC) Deficiency: A Prominent Clinical Finding Among a Series of Ten French PatientsM A Spitz, M A Nguyen, S Roche, et al.
Revue Neurologique|June 1, 2025
French guidelines for the diagnosis and management of pure hereditary spastic paraplegiaL Mania-Pâris, C Ewenczyk, G Nicolas, et al.
Journal of Medical Genetics|August 30, 2008
Refinement of cortical dysgeneses spectrum associated with TUBA1A mutationsN Bahi-Buisson, K Poirier, N Boddaert, et al.
Neurogenetics|March 7, 2008
Is the early-onset torsion dystonia (EOTD) linked to TOR1A gene as frequent as expected in France?M Y Frédéric, F Clot, L Cif, et al.
European Journal of Neurology|June 20, 2020
Deciphering the natural history of SCA7 in childrenM G Bah, D Rodriguez, C Cazeneuve, et al.
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