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Showing results (51-60 of 83) with videos related to

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Multiple Sclerosis (Houndmills, Basingstoke, England)|September 21, 2007
Erythema nodosum and glatiramer acetate treatment in relapsing-remitting multiple sclerosisE Thouvenot, D Hillaire-Buys, M A Bos-Thompson, et al.
Annals of Neurology|February 28, 2001
Compound heterozygous D90A and D96N SOD1 mutations in a recessive amyotrophic lateral sclerosis familyC K Hand, V Mayeux-Portas, J Khoris, et al.
The Canadian Journal of Neurological Sciences. Le Journal Canadien Des Sciences Neurologiques|August 26, 1998
Identification of six novel SOD1 gene mutations in familial amyotrophic lateral sclerosisY Boukaftane, J Khoris, B Moulard, et al.
Neurology|October 29, 2003
Very early onset AD with a de novo mutation in the presenilin 1 gene (Met 233 Leu)F Portet, Y Dauvilliers, D Campion, et al.
Journal of Medical Genetics|October 22, 2008
Contribution of TARDBP mutations to sporadic amyotrophic lateral sclerosisH Daoud, P N Valdmanis, E Kabashi, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|March 30, 2020
Autosomal dominant SPG9: intrafamilial variability and onset during pregnancyC Marelli, S Badiou, S Genestet, et al.
Revue Neurologique|August 24, 2010
[Longitudinal study of health related quality of life in multiple sclerosis: correlation with MRI parameters]M Cohen, C Lebrun, D Aufauvre, et al.
European Journal of Neurology|January 22, 2011
APOE ε4 allele is associated with an increased risk of bulbar-onset amyotrophic lateral sclerosis in menJ Praline, H Blasco, P Vourc'h, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|June 22, 2010
Respiratory onset in an ALS family with L144F SOD1 mutationP Corcia, P Petiot, Z Stevic, et al.
European Journal of Neurology|May 16, 2000
Coexistence of dominant and recessive familial amyotrophic lateral sclerosis with the D90A Cu,Zn superoxide dismutase mutation within the same countryJ Khoris, B Moulard, V Briolotti, et al.
Pageof 9

Showing results (51-60 of 83) with videos related to

Sort By:
Pageof 9
Multiple Sclerosis (Houndmills, Basingstoke, England)|September 21, 2007
Erythema nodosum and glatiramer acetate treatment in relapsing-remitting multiple sclerosisE Thouvenot, D Hillaire-Buys, M A Bos-Thompson, et al.
Annals of Neurology|February 28, 2001
Compound heterozygous D90A and D96N SOD1 mutations in a recessive amyotrophic lateral sclerosis familyC K Hand, V Mayeux-Portas, J Khoris, et al.
The Canadian Journal of Neurological Sciences. Le Journal Canadien Des Sciences Neurologiques|August 26, 1998
Identification of six novel SOD1 gene mutations in familial amyotrophic lateral sclerosisY Boukaftane, J Khoris, B Moulard, et al.
Neurology|October 29, 2003
Very early onset AD with a de novo mutation in the presenilin 1 gene (Met 233 Leu)F Portet, Y Dauvilliers, D Campion, et al.
Journal of Medical Genetics|October 22, 2008
Contribution of TARDBP mutations to sporadic amyotrophic lateral sclerosisH Daoud, P N Valdmanis, E Kabashi, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|March 30, 2020
Autosomal dominant SPG9: intrafamilial variability and onset during pregnancyC Marelli, S Badiou, S Genestet, et al.
Revue Neurologique|August 24, 2010
[Longitudinal study of health related quality of life in multiple sclerosis: correlation with MRI parameters]M Cohen, C Lebrun, D Aufauvre, et al.
European Journal of Neurology|January 22, 2011
APOE ε4 allele is associated with an increased risk of bulbar-onset amyotrophic lateral sclerosis in menJ Praline, H Blasco, P Vourc'h, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|June 22, 2010
Respiratory onset in an ALS family with L144F SOD1 mutationP Corcia, P Petiot, Z Stevic, et al.
European Journal of Neurology|May 16, 2000
Coexistence of dominant and recessive familial amyotrophic lateral sclerosis with the D90A Cu,Zn superoxide dismutase mutation within the same countryJ Khoris, B Moulard, V Briolotti, et al.
Pageof 9