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J-P Azulay

Showing results (121-130 of 133) with videos related to

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Revue Neurologique|April 3, 2001
[Proximal myotonial myopathy (PROMM): clinical and histology study]G Bassez, S Attarian, P Laforêt, et al.
Revue Neurologique|May 3, 2017
Parkinson's disease associated with 22q11.2 deletion: Clinical characteristics and response to treatmentB Dufournet, K Nguyen, P Charles, et al.
Journal of Medical Genetics|February 1, 1993
Emery-Dreifuss muscular dystrophy: linkage to markers in distal Xq28J R Yates, J P Warner, J A Smith, et al.
Revue Neurologique|March 14, 2020
Prevalence and characterisation of vocal fold motion impairment (VFMI) in patients with Multiple system atrophy compared with Parkinson's diseaseS Grimaldi, M Renaud, D Robert, et al.
Neurology|September 30, 2010
Motor activation in multiple system atrophy and Parkinson disease: a PET studyP Payoux, C Brefel-Courbon, F Ory-Magne, et al.
Revue Neurologique|June 20, 2016
French consensus procedure for assessing cognitive function in Parkinson's diseaseK Dujardin, N Auzou, E Lhommée, et al.
NPJ Parkinson'S Disease|December 15, 2020
A randomized controlled double-blind study of rotigotine on neuropsychiatric symptoms in de novo PDA Castrioto, S Thobois, M Anheim, et al.
Revue Neurologique|December 21, 2005
[Chronic inflammatory demyelinating polyradiculoneuropathy: diagnostic strategy. Guidelines of the French CIDP study group]J C Antoine, J P Azulay, P Bouche, et al.
Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology|March 23, 2006
Towards the molecular elucidation of congenital myasthenic syndromes: identification of mutations in MuSKF Chevessier, B Faraut, A Ravel-Chapuis, et al.
Revue Neurologique|September 27, 2021
Validation of a non-motor fluctuations questionnaire in Parkinson's diseaseF Faggianelli, A Loundou, K Baumstarck, et al.
Pageof 14

Showing results (121-130 of 133) with videos related to

Sort By:
Pageof 14
Revue Neurologique|April 3, 2001
[Proximal myotonial myopathy (PROMM): clinical and histology study]G Bassez, S Attarian, P Laforêt, et al.
Revue Neurologique|May 3, 2017
Parkinson's disease associated with 22q11.2 deletion: Clinical characteristics and response to treatmentB Dufournet, K Nguyen, P Charles, et al.
Journal of Medical Genetics|February 1, 1993
Emery-Dreifuss muscular dystrophy: linkage to markers in distal Xq28J R Yates, J P Warner, J A Smith, et al.
Revue Neurologique|March 14, 2020
Prevalence and characterisation of vocal fold motion impairment (VFMI) in patients with Multiple system atrophy compared with Parkinson's diseaseS Grimaldi, M Renaud, D Robert, et al.
Neurology|September 30, 2010
Motor activation in multiple system atrophy and Parkinson disease: a PET studyP Payoux, C Brefel-Courbon, F Ory-Magne, et al.
Revue Neurologique|June 20, 2016
French consensus procedure for assessing cognitive function in Parkinson's diseaseK Dujardin, N Auzou, E Lhommée, et al.
NPJ Parkinson'S Disease|December 15, 2020
A randomized controlled double-blind study of rotigotine on neuropsychiatric symptoms in de novo PDA Castrioto, S Thobois, M Anheim, et al.
Revue Neurologique|December 21, 2005
[Chronic inflammatory demyelinating polyradiculoneuropathy: diagnostic strategy. Guidelines of the French CIDP study group]J C Antoine, J P Azulay, P Bouche, et al.
Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology|March 23, 2006
Towards the molecular elucidation of congenital myasthenic syndromes: identification of mutations in MuSKF Chevessier, B Faraut, A Ravel-Chapuis, et al.
Revue Neurologique|September 27, 2021
Validation of a non-motor fluctuations questionnaire in Parkinson's diseaseF Faggianelli, A Loundou, K Baumstarck, et al.
Pageof 14