Multiple Sclerosis Discovery Forum

Inspiring Connections

Most Viewed

Erythropoietin reduces white matter damage in two-day-old rats exposed to hypoxic/ischemia injury.
Treatment of the osmotic demyelination syndrome: the earlier the better?
Clinical insights for early detection of acute transverse myelitis in the emergency department.
Anti-MAG autoantibodies are increased in Parkinson's disease but not in atypical parkinsonism.
Should the symptomatic region be included in dissemination in space in MRI criteria for MS?
Identification of the Kappa-Opioid Receptor as a Therapeutic Target for Oligodendrocyte Remyelination.
Metabolic profiling reveals biochemical pathways and potential biomarkers associated with the pathogenesis of Krabbe disease.
Percutaneous Endoscopic Gastrostomy Tube Insertion in Neurodegenerative Disease: A Retrospective Study and Literature Review.
Astrocyte-mediated infantile-onset leukoencephalopathy mouse model.
Major Superficial White Matter Abnormalities in Huntington's Disease.
Expression of IL-1β in rhesus EAE and MS lesions is mainly induced in the CNS itself.
Gray matter-related proteins are associated with childhood-onset multiple sclerosis.
Visual impairment.
Efficacy of Polyvalent Human Immunoglobulins in an Animal Model of Neuromyelitis Optica Evoked by Intrathecal Anti-Aquaporin 4 Antibodies.
Functional Magnetic Resonance Imaging with Concurrent Urodynamic Testing Identifies Brain Structures Involved in Micturition Cycle in Patients with Multiple Sclerosis.
A review of the ethics of the use of placebo in clinical trials for relapsing-remitting multiple sclerosis therapeutics.
[The correlation factor analysis for conversion of clinically isolated syndrome to multiple sclerosis and neuromyelitis optica].
Scrub Typhus Causing Unilateral Optic Neuritis.
Money Management Activities in Persons with Multiple Sclerosis.
Multiple sclerosis and primary vascular dysregulation (Flammer syndrome).
DNA Methylation: a New Player in Multiple Sclerosis.
Levels and Rates of Physical Activity in Older Adults with Multiple Sclerosis.
Longitudinal Study of Retinal Nerve Fiber Layer Thickness and Macular Volume in Patients With Neuromyelitis Optica Spectrum Disorder.
A family with hereditary diffuse leukoencephalopathy with spheroids caused by a novel c.2442+2T>C mutation in the CSF1R gene.
Expanding the range of immunopathology in neuromyelitis optica spectrum disorder.

Pages