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Showing results (91-100 of 100) with videos related to

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Revue Neurologique|September 21, 2023
French National Protocol for genetic of amyotrophic lateral sclerosisP Corcia, P Vourc'h, E Bernard, et al.
Neurogenetics|March 25, 2000
Mutations in the X-linked form of Charcot-Marie-Tooth disease in the French populationP Latour, N Lévy, M Paret, et al.
The Journal of Nutrition, Health & Aging|December 2, 2008
Rapid cognitive decline in Alzheimer's disease. Consensus paperM E Soto, S Andrieu, C Arbus, et al.
European Journal of Neurology|February 3, 2016
Evaluation of the application of the European guidelines for the diagnosis and clinical care of amyotrophic lateral sclerosis (ALS) patients in six French ALS centresB Marin, E Beghi, C Vial, et al.
Revue Neurologique|May 21, 2026
Primary Lateral Sclerosis French National Diagnostic and Care ProtocolP Corcia, E Bernard, E de la Cruz, et al.
Neurology|April 28, 2012
Phenotype and genotype analysis in amyotrophic lateral sclerosis with TARDBP gene mutationsP Corcia, P Valdmanis, S Millecamps, et al.
European Journal of Neurology|November 1, 2008
Causes of death amongst French patients with amyotrophic lateral sclerosis: a prospective studyJ Gil, B Funalot, A Verschueren, et al.
Neurology|May 13, 2009
Chromosome 9p-linked families with frontotemporal dementia associated with motor neuron diseaseI Le Ber, A Camuzat, E Berger, et al.
Revue Neurologique|February 17, 2009
[Internet and amyotrophic lateral sclerosis treatment: what is wrong?]V Meininger, J-C Antoine, M C Arne-Bes, et al.
European Journal of Neurology|August 2, 2025
Prevalence of SOD1 and C9orf72 Variants Among French ALS Population: The GENIALS StudyP Corcia, D Erazo, M D M Amador, et al.
Pageof 10

Showing results (91-100 of 100) with videos related to

Sort By:
Pageof 10
You have reached the last page of results.This site can display upto 100 results.
Revue Neurologique|September 21, 2023
French National Protocol for genetic of amyotrophic lateral sclerosisP Corcia, P Vourc'h, E Bernard, et al.
Neurogenetics|March 25, 2000
Mutations in the X-linked form of Charcot-Marie-Tooth disease in the French populationP Latour, N Lévy, M Paret, et al.
The Journal of Nutrition, Health & Aging|December 2, 2008
Rapid cognitive decline in Alzheimer's disease. Consensus paperM E Soto, S Andrieu, C Arbus, et al.
European Journal of Neurology|February 3, 2016
Evaluation of the application of the European guidelines for the diagnosis and clinical care of amyotrophic lateral sclerosis (ALS) patients in six French ALS centresB Marin, E Beghi, C Vial, et al.
Revue Neurologique|May 21, 2026
Primary Lateral Sclerosis French National Diagnostic and Care ProtocolP Corcia, E Bernard, E de la Cruz, et al.
Neurology|April 28, 2012
Phenotype and genotype analysis in amyotrophic lateral sclerosis with TARDBP gene mutationsP Corcia, P Valdmanis, S Millecamps, et al.
European Journal of Neurology|November 1, 2008
Causes of death amongst French patients with amyotrophic lateral sclerosis: a prospective studyJ Gil, B Funalot, A Verschueren, et al.
Neurology|May 13, 2009
Chromosome 9p-linked families with frontotemporal dementia associated with motor neuron diseaseI Le Ber, A Camuzat, E Berger, et al.
Revue Neurologique|February 17, 2009
[Internet and amyotrophic lateral sclerosis treatment: what is wrong?]V Meininger, J-C Antoine, M C Arne-Bes, et al.
European Journal of Neurology|August 2, 2025
Prevalence of SOD1 and C9orf72 Variants Among French ALS Population: The GENIALS StudyP Corcia, D Erazo, M D M Amador, et al.
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