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C Brefel-Courbon

Showing results (41-50 of 47) with videos related to

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Revue Neurologique|August 26, 2023
Impact of therapeutic education on the evolution of social representations of medication in patients with Parkinson's disease: A quantitative and qualitative study (ETPARK REMED)I Faurie, E Harroch, C Scotto d'Apollonia, 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.
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.
American Journal of Human Genetics|February 17, 2001
Origin of the mutations in the parkin gene in Europe: exon rearrangements are independent recurrent events, whereas point mutations may result from Founder effectsM Periquet, C Lücking, J Vaughan, 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.
Human Molecular Genetics|March 11, 1999
A wide variety of mutations in the parkin gene are responsible for autosomal recessive parkinsonism in Europe. French Parkinson's Disease Genetics Study Group and the European Consortium on Genetic Susceptibility in Parkinson's DiseaseN Abbas, C B Lücking, S Ricard, 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 5

Showing results (41-50 of 47) with videos related to

Sort By:
Pageof 5
You have reached the last page of results.This site can display upto 47 results.
Revue Neurologique|August 26, 2023
Impact of therapeutic education on the evolution of social representations of medication in patients with Parkinson's disease: A quantitative and qualitative study (ETPARK REMED)I Faurie, E Harroch, C Scotto d'Apollonia, 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.
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.
American Journal of Human Genetics|February 17, 2001
Origin of the mutations in the parkin gene in Europe: exon rearrangements are independent recurrent events, whereas point mutations may result from Founder effectsM Periquet, C Lücking, J Vaughan, 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.
Human Molecular Genetics|March 11, 1999
A wide variety of mutations in the parkin gene are responsible for autosomal recessive parkinsonism in Europe. French Parkinson's Disease Genetics Study Group and the European Consortium on Genetic Susceptibility in Parkinson's DiseaseN Abbas, C B Lücking, S Ricard, 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 5