Multiple Sclerosis Discovery Forum

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Natalizumab in the pediatric MS population: results of the Italian registry.
The association between olfactory bulb volume, cognitive dysfunction, physical disability and depression in multiple sclerosis.
Evidence for classic complement activity in neuromyelitis optica.
Potassium channel KIR4.1-specific antibodies in children with acquired demyelinating CNS disease.
Lingo-1 Inhibited by RNA Interference Promotes Functional Recovery of Experimental Autoimmune Encephalomyelitis.
Mesenchymal Stem Cell-Based Therapy in a Mouse Model of Experimental Autoimmune Encephalomyelitis (EAE).
Low and High CD8 Positive T cells in Multiple Sclerosis Patients.
Observational Study Assessing Demographic, Economic and Clinical Factors Associated with Access and Utilization of Health Care Services of Patients with Multiple Sclerosis under Treatment with Interferon Beta-1b (EXTAVIA).
Cognitive impairment in Chinese neuromyelitis optica.
Enrichment of Oligodendrocyte Progenitors from Differentiated Neural Precursors by Clonal Sphere Preparations.
[Translation and cross-cultural adaptation of the Multiple Sclerosis Walking Scale (MSWS-12) into Brazilian Portuguese].
[Neuromyelitis optica in children. Two case reports.]
What is needed to keep persons with multiple sclerosis vitamin D-sufficient throughout the year?
The impact of osteopontin gene variations on multiple sclerosis development and progression.
Hemianopia and visual loss due to progressive multifocal leukoencephalopathy in natalizumab-treated multiple sclerosis.
Distress associated with patients' symptoms and depression in a sample of Mexican caregivers of individuals with MS.
Expansion of Functional Human Mucosal-Associated Invariant T Cells via Reprogramming to Pluripotency and Redifferentiation.
Management of Secondary Progressive Multiple Sclerosis: Prophylactic Treatment-Past, Present, and Future Aspects.
Procedural Variations in the Stroop and the Symbol Digit Modalities Test: Impact on Patients with Multiple Sclerosis.
Risk of relapse phenotype recurrence in multiple sclerosis.
Role of p38MAPK in S1P receptor-mediated differentiation of human oligodendrocyte progenitors.
Disability Identity Predicts Lower Anxiety and Depression in Multiple Sclerosis.
Epigenetic changes in neurology: DNA methylation in multiple sclerosis.
CENTENARIAN RATES AND LIFE EXPECTANCY RELATED TO THE DEATH RATES OF MULTIPLE SCLEROSIS, ASTHMA AND RHEUMATOID ARTHRITIS AND THE INCIDENCE OF TYPE 1 DIABETES IN CHILDREN.
The Latest Innovations in the Drug Pipeline for Multiple Sclerosis.

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