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Human Immunology
|
December 18, 2007
The autoimmune disease-associated IL12B and IL23R polymorphisms in multiple sclerosis
Ann B Begovich, Monica Chang, Stacy J Caillier, et al.
Annals of Neurology
|
October 17, 2020
Retinal INL Thickness in Multiple Sclerosis: A Mere Marker of Neurodegeneration?
Christian Cordano, Hao H Yiu, Frederike C Oertel, et al.
Multiple Sclerosis (Houndmills, Basingstoke, England)
|
September 11, 2023
Efficacy and safety of four-year ofatumumab treatment in relapsing multiple sclerosis: The ALITHIOS open-label extension
Stephen L Hauser, Ronald Zielman, Ayan Das Gupta, et al.
Multiple Sclerosis (Houndmills, Basingstoke, England)
|
December 20, 2018
Slowly expanding/evolving lesions as a magnetic resonance imaging marker of chronic active multiple sclerosis lesions
Colm Elliott, Jerry S Wolinsky, Stephen L Hauser, et al.
American Journal of Human Genetics
|
December 8, 2004
The R620W polymorphism of the protein tyrosine phosphatase PTPN22 is not associated with multiple sclerosis
Ann B Begovich, Stacy J Caillier, Heather C Alexander, et al.
European Journal of Neurology
|
March 16, 2021
Risk of requiring a walking aid after 6.5 years of ocrelizumab treatment in patients with relapsing multiple sclerosis: Data from the OPERA I and OPERA II trials
Gavin Giovannoni, Ludwig Kappos, Jerome de Seze, et al.
Annals of Neurology
|
January 13, 2018
Thalamic atrophy in multiple sclerosis: A magnetic resonance imaging marker of neurodegeneration throughout disease
Christina J Azevedo, Steven Y Cen, Sankalpa Khadka, et al.
Annals of Neurology
|
January 23, 2014
Quo vadis? Peering into the future
Stephen L Hauser, S Claiborne Johnston, Donna M Ferriero, et al.
Journal of Neuroimaging : Official Journal of the American Society of Neuroimaging
|
October 2, 2019
Intersubject Variability and Normalization Strategies for Spinal Cord Total Cross-Sectional and Gray Matter Areas
Nico Papinutto, Carlo Asteggiano, Antje Bischof, et al.
Human Molecular Genetics
|
December 3, 2005
Association of the truncating splice site mutation in BTNL2 with multiple sclerosis is secondary to HLA-DRB1*15
James A Traherne, Lisa F Barcellos, Stephen J Sawcer, et al.
Page
of 33
Search research articles
Search
Showing results (131-140 of 322) with videos related to
Sort By:
Page
of 33
Human Immunology
|
December 18, 2007
The autoimmune disease-associated IL12B and IL23R polymorphisms in multiple sclerosis
Ann B Begovich, Monica Chang, Stacy J Caillier, et al.
Annals of Neurology
|
October 17, 2020
Retinal INL Thickness in Multiple Sclerosis: A Mere Marker of Neurodegeneration?
Christian Cordano, Hao H Yiu, Frederike C Oertel, et al.
Multiple Sclerosis (Houndmills, Basingstoke, England)
|
September 11, 2023
Efficacy and safety of four-year ofatumumab treatment in relapsing multiple sclerosis: The ALITHIOS open-label extension
Stephen L Hauser, Ronald Zielman, Ayan Das Gupta, et al.
Multiple Sclerosis (Houndmills, Basingstoke, England)
|
December 20, 2018
Slowly expanding/evolving lesions as a magnetic resonance imaging marker of chronic active multiple sclerosis lesions
Colm Elliott, Jerry S Wolinsky, Stephen L Hauser, et al.
American Journal of Human Genetics
|
December 8, 2004
The R620W polymorphism of the protein tyrosine phosphatase PTPN22 is not associated with multiple sclerosis
Ann B Begovich, Stacy J Caillier, Heather C Alexander, et al.
European Journal of Neurology
|
March 16, 2021
Risk of requiring a walking aid after 6.5 years of ocrelizumab treatment in patients with relapsing multiple sclerosis: Data from the OPERA I and OPERA II trials
Gavin Giovannoni, Ludwig Kappos, Jerome de Seze, et al.
Annals of Neurology
|
January 13, 2018
Thalamic atrophy in multiple sclerosis: A magnetic resonance imaging marker of neurodegeneration throughout disease
Christina J Azevedo, Steven Y Cen, Sankalpa Khadka, et al.
Annals of Neurology
|
January 23, 2014
Quo vadis? Peering into the future
Stephen L Hauser, S Claiborne Johnston, Donna M Ferriero, et al.
Journal of Neuroimaging : Official Journal of the American Society of Neuroimaging
|
October 2, 2019
Intersubject Variability and Normalization Strategies for Spinal Cord Total Cross-Sectional and Gray Matter Areas
Nico Papinutto, Carlo Asteggiano, Antje Bischof, et al.
Human Molecular Genetics
|
December 3, 2005
Association of the truncating splice site mutation in BTNL2 with multiple sclerosis is secondary to HLA-DRB1*15
James A Traherne, Lisa F Barcellos, Stephen J Sawcer, et al.
Page
of 33