Search research articles
Contact Us
Filters
Showing results (71-80 of 83) with videos related to
Page
of 9
Sort By:
Neurology
|
April 28, 2012
Phenotype and genotype analysis in amyotrophic lateral sclerosis with TARDBP gene mutations
P Corcia, P Valdmanis, S Millecamps, et al.
Neurology
|
September 11, 2009
Mutations in FUS cause FALS and SALS in French and French Canadian populations
V 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 factor
A 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 study
J 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 assay
I 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 study
N Collongues, R Marignier, H Zéphir, et al.
Neurology
|
May 13, 2009
Chromosome 9p-linked families with frontotemporal dementia associated with motor neuron disease
I 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 cohort
O Outteryck, J C Ongagna, B Brochet, et al.
Neurology
|
March 3, 2010
Neuromyelitis optica in France: a multicenter study of 125 patients
N 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.
Page
of 9
Search research articles
Search
Showing results (71-80 of 83) with videos related to
Sort By:
Page
of 9
Neurology
|
April 28, 2012
Phenotype and genotype analysis in amyotrophic lateral sclerosis with TARDBP gene mutations
P Corcia, P Valdmanis, S Millecamps, et al.
Neurology
|
September 11, 2009
Mutations in FUS cause FALS and SALS in French and French Canadian populations
V 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 factor
A 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 study
J 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 assay
I 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 study
N Collongues, R Marignier, H Zéphir, et al.
Neurology
|
May 13, 2009
Chromosome 9p-linked families with frontotemporal dementia associated with motor neuron disease
I 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 cohort
O Outteryck, J C Ongagna, B Brochet, et al.
Neurology
|
March 3, 2010
Neuromyelitis optica in France: a multicenter study of 125 patients
N 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.
Page
of 9