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Showing results (61-70 of 69) with videos related to

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Journal of Medical Genetics|June 23, 2009
Penetrance of marked cognitive impairment in older male carriers of the FMR1 gene premutationM Sévin, Z Kutalik, S Bergman, et al.
Advances in Neurology|November 22, 2002
Parkinson's disease is a neuropsychiatric disorderY Agid, I Arnulf, P Bejjani, et al.
Revue Neurologique|February 24, 2026
Simulated shared and supported decision making for amyloid immunotherapy in Alzheimer's disease: A bicentric studyE Burry, F Plumacker, N Villain, 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.
European Journal of Neurology|September 30, 2017
High-dose transdermal nicotine in Parkinson's disease patients: a randomized, open-label, blinded-endpoint evaluation phase 2 studyG Villafane, C Thiriez, E Audureau, et al.
Journal of Medical Genetics|April 10, 2009
Molecular analyses of the LRRK2 gene in European and North African autosomal dominant Parkinson's diseaseS Lesage, C Condroyer, A Lannuzel, 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.
The New England Journal of Medicine|February 15, 2013
Neurostimulation for Parkinson's disease with early motor complicationsW M M Schuepbach, J Rau, K Knudsen, et al.
Pageof 7

Showing results (61-70 of 69) with videos related to

Sort By:
Pageof 7
You have reached the last page of results.This site can display upto 69 results.
Journal of Medical Genetics|June 23, 2009
Penetrance of marked cognitive impairment in older male carriers of the FMR1 gene premutationM Sévin, Z Kutalik, S Bergman, et al.
Advances in Neurology|November 22, 2002
Parkinson's disease is a neuropsychiatric disorderY Agid, I Arnulf, P Bejjani, et al.
Revue Neurologique|February 24, 2026
Simulated shared and supported decision making for amyloid immunotherapy in Alzheimer's disease: A bicentric studyE Burry, F Plumacker, N Villain, 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.
European Journal of Neurology|September 30, 2017
High-dose transdermal nicotine in Parkinson's disease patients: a randomized, open-label, blinded-endpoint evaluation phase 2 studyG Villafane, C Thiriez, E Audureau, et al.
Journal of Medical Genetics|April 10, 2009
Molecular analyses of the LRRK2 gene in European and North African autosomal dominant Parkinson's diseaseS Lesage, C Condroyer, A Lannuzel, 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.
The New England Journal of Medicine|February 15, 2013
Neurostimulation for Parkinson's disease with early motor complicationsW M M Schuepbach, J Rau, K Knudsen, et al.
Pageof 7