Multiple Sclerosis Discovery Forum

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Most Viewed Papers

HLA-DR15 haplotype and multiple sclerosis: a HuGE review.
The hGFAP-driven conditional TSPO knockout is protective in a mouse model of multiple sclerosis.
Hypoxia-inducible factor 1 in autoimmune diseases.
Shifting paradigms in multiple sclerosis: from disease-specific, through population-specific toward patient-specific.
Assessing the Risk Factors for Multiple Sclerosis in Women of Reproductive Age Suffering the Disease in Isfahan Province.
Erratum: Genomic analysis of ERVWE2 locus in patients with Multiple sclerosis: absence of genetic association but potential role of Human Endogenous retrovirus type W elements in molecular mimicry with myelin antigen.
Alphab-crystallin is a target for adaptive immune responses and a trigger of innate responses in preactive multiple sclerosis lesions.
Catalytic autoantibodies against myelin basic protein (MBP) isolated from serum of autistic children impair in vitro models of synaptic plasticity in rat hippocampus.
Sex bias in CNS autoimmune disease mediated by androgen control of autoimmune regulator.
Impacts of education level and employment status on health-related quality of life in multiple sclerosis patients.
Cellulose/soy protein composite-based nerve guidance conduits with designed microstructure for peripheral nerve regeneration.
Endocannabinoid pathways and their role in multiple sclerosis-related muscular dysfunction.
Cortical lesion counts by double inversion recovery should be part of the MRI monitoring process for all MS patients: No.
Molecular dynamics and intracellular signaling of the TNF-R1 with the R92Q mutation.
Bypassing hazard of housekeeping genes: their evaluation in rat granule neurons treated with cerebrospinal fluid of multiple sclerosis subjects.
What do we know about brain contrast enhancement patterns in neuromyelitis optica?
Neurosarcoidosis: Clinical Features, Diagnosis, and Management.
NADPH oxidase 2 (NOX2) enzyme activation in patients with chronic inflammatory demyelinating polyneuropathy.
A promiscuous recognition mechanism between GPR17 and SDF-1: Molecular insights.
Osmotic demyelination syndrome complicating diabetes with anti-glutamic acid decarboxylase antibodies and Graves' disease: A case report.
Tumour suppressor death-associated protein kinase targets cytoplasmic HIF-1α for Th17 suppression.
[Pathology, diagnosis, and treatment of combined central and peripheral demyelination].
A Novel Asp121Asn Mutation of Myelin Protein Zero Is Associated with Late-Onset Axonal Charcot-Marie-Tooth Disease, Hearing Loss and Pupil Abnormalities.
Deep morphea induced by interferon-β1b injection.
X-ray radiation and the risk of multiple sclerosis: Do the site and dose of exposure matter?

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