Multiple Sclerosis Discovery Forum

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Most Viewed Papers

The poor recovery of neuromyelitis optica spectrum disorder is associated with a lower level of CXCL12 in the human brain.
Multiple Sclerosis between Genetics and Infections: Human Endogenous Retroviruses in Monocytes and Macrophages.
Restless legs syndrome in multiple sclerosis.
Long-term remission of CIDP after pulsed dexamethasone or short-term prednisolone treatment.
Interleukin-10 Gene-transfected Mature Dendritic Cells Suppress Murine Experimental Autoimmune Optic Neuritis.
Studies in Experimental Autoimmune Encephalomyelitis Do Not Support Developmental Bisphenol A Exposure as an Environmental Factor in Increasing Multiple Sclerosis Risk.
The Effects of Threonine Phosphorylation on the Stability and Dynamics of the Central Molecular Switch Region of 18.5-kDa Myelin Basic Protein.
Screening for neurotropic viruses in cerebrospinal fluid of patients with multiple sclerosis and other neurological diseases.
Guideline for the diagnosis and management of multiple sclerosis: A Southern African perspective.
Does MOG Ig-positive AQP4-seronegative opticospinal inflammatory disease justify a diagnosis of NMO spectrum disorder?
Attitude towards physical activity in patients with multiple sclerosis: a cohort study.
DOPAMINE AND T CELLS: Receptors, Direct and Potent Effects, Endogenous Production and Abnormalities in Autoimmune, Neurological and Psychiatric Diseases.
XY sex chromosome complement, compared with XX, in the CNS confers greater neurodegeneration during experimental autoimmune encephalomyelitis.
Ischemic Retinal Vasculitis and Its Management.
Methods for identifying subject-specific abnormalities in neuroimaging data.
Human recombinant domain antibodies against multiple sclerosis antigenic peptide CSF114(Glc).
OGR1/GPR68 Modulates the Severity of Experimental Autoimmune Encephalomyelitis and Regulates Nitric Oxide Production by Macrophages.
Differential screening-selected gene aberrative in neuroblastoma (DAN) is increased in the CSF of patients with MS and may be induced by therapy with interferon-β.
Laquinimod in the treatment of multiple sclerosis: a review of the data so far.
Heterogeneity of cortical lesions in multiple sclerosis: an MRI perfusion study.
Genome-wide significant association of ANKRD55 rs6859219 and multiple sclerosis risk.
Critical role of the Mac1/NOX2 pathway in mediating reactive microgliosis-generated chronic neuroinflammation and progressive neurodegeneration.
Clinical variability and female penetrance in X-linked familial FTD/ALS caused by a P506S mutation in UBQLN2.
Depressive syndromes in neurological disorders.
Maintenance percutaneous posterior nerve stimulation for refractory lower urinary tract symptoms in patients with multiple sclerosis.

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