Multiple Sclerosis Discovery Forum

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Pharmacological treatments for fatigue associated with palliative care.
Status epilepticus associated with dalfampridine in a patient with multiple sclerosis.
Oligodendrocyte N-Methyl-D-aspartate Receptor Signaling: Insights into Its Functions.
Concomitant neuromyelitis optica and cytomegalovirus-associated retinitis in an immunocompetent female.
The amyloid state of proteins in human diseases.
Chemokine receptor expression by inflammatory T cells in EAE.
B-61Impact of Sleep Quality, Depression, Daytime Sleepiness, and Fatigue on Cognition in Multiple Sclerosis.
Coenzyme Q10 supplementation and multiple sclerosis.
Neutrophils Mediate Blood-Spinal Cord Barrier Disruption in Demyelinating Neuroinflammatory Diseases.
Seminal vesicle fluid ameliorates experimental autoimmune encephalomyelitis by increasing FoxP3(+) regulatory T-cell numbers.
How do we manage and treat a patient with multiple sclerosis at risk of tuberculosis?
Hit-to-lead evaluation of a novel class of sphingosine 1-phosphate lyase inhibitors.
Is the Relationship between Cortical and White Matter Pathologic Changes in Multiple Sclerosis Spatially Specific? A Multimodal 7-T and 3-T MR Imaging Study with Surface and Tract-based Analysis.
Translating CESD-20 and PHQ-9 Scores to PROMIS Depression.
Therapeutic promises of 2-methoxyestradiol and its drug disposition challenges.
Isolated and persistent cognitive dysfunction in a patient with acute disseminated encephalomyelitis.
Comparative Effects of Human Neural Stem Cells and Oligodendrocyte Progenitor Cells on the Neurobehavioral Disorders of Experimental Autoimmune Encephalomyelitis Mice.
Monitoring interferon β treatment response with magnetic resonance spectroscopy in relapsing remitting multiple sclerosis.
Treatment-resistant immune thrombocytopenic purpura associated with LDN use in a patient with MS.
Can meditation influence quality of life, depression, and disease outcome in multiple sclerosis? Findings from a large international web-based study.
Susceptibility genes are enriched in those of the HSV-1/host interactome in psychiatric and neurological disorders.
Founder mutations in NDRG1 and HK1 genes are common causes of inherited neuropathies among Roma/Gypsies in Slovakia.
Change in quality of life and predictors of change among patients with multiple sclerosis: a prospective cohort study.
Central motor conduction time.
Attributional style and depression in multiple sclerosis: the learned helplessness model.

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