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Most Viewed Papers
Connectivity-based parcellation of the thalamus in multiple sclerosis and its implications for cognitive impairment: A multicenter study.
Quantitative sensory and motor measures detect change over time and correlate with walking speed in individuals with multiple sclerosis.
Experimental Autoimmune Encephalomyelitis in Marmosets.
Therapeutic Advances and Future Prospects in Progressive Forms of Multiple Sclerosis.
Retinoic acid suppresses IL-17 production and pathogenic activity of γδ T cells in CNS autoimmunity.
A Reversible and Selective Inhibitor of Monoacylglycerol Lipase Ameliorates Multiple Sclerosis.
Acupuncture and multiple sclerosis: a review of the evidence.
Expression and Genetic Analysis of MicroRNAs Involved in Multiple Sclerosis.
White-matter lesions drive deep gray-matter atrophy in early multiple sclerosis: support from structural MRI.
The rehabilitation of the multiple sclerosis patient.
Polyarteritis nodosa with central nervous system involvement mimicking relapsing-remitting multiple sclerosis.
Treating prolactinoma can prevent autoimmune diseases.
Corneal confocal microscopy in chronic inflammatory demyelinating polyneuropathy.
Validation of the PASAT in Argentina.
Translation, cross-cultural adaptation and validation of the Portuguese version of the DYMUS questionnaire for the assessment of dysphagia in multiple sclerosis.
Cytokine-Defined B Cell Responses as Therapeutic Targets in Multiple Sclerosis.
ACTH protects mature oligodendroglia from excitotoxic and inflammation-related damage in vitro.
Endogenous and synthetic MMP inhibitors in CNS physiopathology.
Oligoclonal bands in multiple sclerosis patients: worse prognosis?
Onion-shaped white matter disease?
MAL Overexpression Leads to Disturbed Expression of Genes That Influence Cytoskeletal Organization and Differentiation of Schwann Cells.
Smoking and risk of treatment-induced neutralizing antibodies to interferon β-1a.
Genome-Wide DNA Methylation Profiles Indicate CD8+ T Cell Hypermethylation in Multiple Sclerosis.
Theiler's murine encephalomyelitis virus as an experimental model system to study the mechanism of blood-brain barrier disruption.
A case of hereditary diffuse leukoencephalopathy with axonal spheroids caused by a de novo mutation in CSF1R masquerading as primary progressive multiple sclerosis.
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