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Showing results (71-80 of 83) with videos related to

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Neurology|April 28, 2012
Phenotype and genotype analysis in amyotrophic lateral sclerosis with TARDBP gene mutationsP Corcia, P Valdmanis, S Millecamps, et al.
Neurology|September 11, 2009
Mutations in FUS cause FALS and SALS in French and French Canadian populationsV V Belzil, P N Valdmanis, P A Dion, et al.
Human Molecular Genetics|November 18, 1998
Recessive amyotrophic lateral sclerosis families with the D90A SOD1 mutation share a common founder: evidence for a linked protective factorA Al-Chalabi, P M Andersen, B Chioza, 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.
Clinical Immunology (Orlando, Fla.)|December 31, 2010
Strategy for anti-aquaporin-4 auto-antibody identification and quantification using a new cell-based assayI De Vidi, G Boursier, N Delouche, et al.
Multiple Sclerosis (Houndmills, Basingstoke, England)|January 18, 2011
High-risk syndrome for neuromyelitis optica: a descriptive and comparative studyN Collongues, R Marignier, H Zéphir, 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.
European Journal of Neurology|July 31, 2013
A prospective observational post-marketing study of natalizumab-treated multiple sclerosis patients: clinical, radiological and biological features and adverse events. The BIONAT cohortO Outteryck, J C Ongagna, B Brochet, et al.
Neurology|March 3, 2010
Neuromyelitis optica in France: a multicenter study of 125 patientsN Collongues, R Marignier, H Zéphir, 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.
Pageof 9

Showing results (71-80 of 83) with videos related to

Sort By:
Pageof 9
Neurology|April 28, 2012
Phenotype and genotype analysis in amyotrophic lateral sclerosis with TARDBP gene mutationsP Corcia, P Valdmanis, S Millecamps, et al.
Neurology|September 11, 2009
Mutations in FUS cause FALS and SALS in French and French Canadian populationsV V Belzil, P N Valdmanis, P A Dion, et al.
Human Molecular Genetics|November 18, 1998
Recessive amyotrophic lateral sclerosis families with the D90A SOD1 mutation share a common founder: evidence for a linked protective factorA Al-Chalabi, P M Andersen, B Chioza, 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.
Clinical Immunology (Orlando, Fla.)|December 31, 2010
Strategy for anti-aquaporin-4 auto-antibody identification and quantification using a new cell-based assayI De Vidi, G Boursier, N Delouche, et al.
Multiple Sclerosis (Houndmills, Basingstoke, England)|January 18, 2011
High-risk syndrome for neuromyelitis optica: a descriptive and comparative studyN Collongues, R Marignier, H Zéphir, 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.
European Journal of Neurology|July 31, 2013
A prospective observational post-marketing study of natalizumab-treated multiple sclerosis patients: clinical, radiological and biological features and adverse events. The BIONAT cohortO Outteryck, J C Ongagna, B Brochet, et al.
Neurology|March 3, 2010
Neuromyelitis optica in France: a multicenter study of 125 patientsN Collongues, R Marignier, H Zéphir, 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.
Pageof 9