Multiple Sclerosis Discovery Forum

Inspiring Connections

Most Viewed Papers

Expanding the range of immunopathology in neuromyelitis optica spectrum disorder.
Tiam1/Rac1 complex controls Il17a transcription and autoimmunity.
Serum BAFF levels, Methypredsinolone therapy, Epstein-Barr Virus and Mycobacterium avium subsp. paratuberculosis infection in Multiple Sclerosis patients.
Spermidine alleviates experimental autoimmune encephalomyelitis through inducing inhibitory macrophages.
Key Points for Issue.
Sunlight exposure: Do health benefits outweigh harm?
Opposite Interplay between PPAR Gamma and Canonical Wnt/Beta-Catenin Pathway in Amyotrophic Lateral Sclerosis.
>CME/CNE ARTICLE: Severity Grading in Multiple Sclerosis: A Proposal.
Myelopathy.
β cell ER stress and the implications for immunogenicity in type 1 diabetes.
Multiple sclerosis and primary vascular dysregulation (Flammer syndrome).
Inhaled Sargramostim Induces Resolution of Pulmonary Alveolar Proteinosis in Lysinuric Protein Intolerance.
Peripheral neuropathies.
Structural brain anomalies in healthy adolescents in the NCANDA cohort: relation to neuropsychological test performance, sex, and ethnicity.
Interferon-β therapy specifically reduces pathogenic memory B cells in Multiple Sclerosis patients by inducing a FAS-mediated apoptosis.
g-Ratio weighted imaging of the human spinal cord in vivo.
Lesson of the month 1: Post-malaria neurological syndromes.
[Transverse myelitis associated with toxocariasis and the importance of locally produced antibodies for diagnosis].
Orofacial evaluation in patients with multiple sclerosis using Nordic Orofacial Test-Screening.
Improved Simulation of Electrodiffusion in the Node of Ranvier by Mesh Adaptation.
Relationship between Visual Dysfunction and Retinal Changes in Patients with Multiple Sclerosis.
Redox Events As Modulators of Pathology and Therapy of Neuroinflammatory Diseases.
In vivo nanoparticle imaging of innate immune cells can serve as a marker of disease severity in a model of multiple sclerosis.
A family with hereditary diffuse leukoencephalopathy with spheroids caused by a novel c.2442+2T>C mutation in the CSF1R gene.
Physician Prescribing Practices of Vitamin D in a Psychiatric Hospital.

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