Multiple Sclerosis Discovery Forum

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Gain of Olig2 function in oligodendrocyte progenitors promotes remyelination.
Co-occurrence of multiple sclerosis and Thomsen's myotonia: a report of two cases.
Scale Adjustments to Facilitate Two-Dimensional Measurements in OCT Images.
Myelination: Actin Disassembly Leads the Way.
Substrate stiffness of endothelial cells directs LFA-1/ICAM-1 interaction: A physical trigger of immune-related diseases?
Molecular alterations of the blood-brain barrier under inflammatory conditions: The role of endothelial to mesenchymal transition.
VDJtools: Unifying Post-analysis of T Cell Receptor Repertoires.
Anatomical and functional retinal changes in multiple sclerosis.
A role for sex chromosome complement in the female bias in autoimmune disease.
Meningoencephalitis-like onset of post-infectious AQP4-IgG-positive optic neuritis complicated by GM1-IgG-positive acute polyneuropathy.
Cervical spinal cord volume loss is related to clinical disability progression in multiple sclerosis.
Increased thalamic intrinsic oscillation amplitude in relapsing-remitting multiple sclerosis associated with the slowed cognitive processing.
The potential of epigenetic therapies in neurodegenerative diseases.
Diagnosing MS: recognizing common symptoms and interpreting MRI results.
HINT1 peptide/Hsp70 complex induces NK cell-dependent immunoregulation in a model of autoimmune demyelination.
How do we manage and treat a patient with multiple sclerosis at risk of tuberculosis?
Demographic and clinical profile of myelopathy patients.
Selective upregulation of scavenger receptors in and around demyelinating areas in multiple sclerosis.
[Multiple sclerosis: a comprehensive treatment and rehabilitation].
Promising New Approaches to Assess Cognitive Functioning in People with Multiple Sclerosis.
Role of regulatory T cells in pathogenesis and biological therapy of multiple sclerosis.
PRISM: A Novel Research Tool to Assess the Prevalence of Pseudobulbar Affect Symptoms across Neurological Conditions.
Founder mutations in NDRG1 and HK1 genes are common causes of inherited neuropathies among Roma/Gypsies in Slovakia.
Delayed Recovery of Leg Fatigue Symptoms Following a Maximal Exercise Session in People With Multiple Sclerosis.
Pediatric Inflammatory Diseases. Part II: Acute Post-Infectious Immune Disorders.

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