Multiple Sclerosis Discovery Forum

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An acute transverse myelitis attack after total body irradiation: a rare case.
Changes in normal appearing spinal cord in multiple sclerosis: another brick in the wall.
Increased Circulating Th17 Cell Populations and Elevated CSF Osteopontin and IL-17 Concentrations in Patients with Guillain-Barré Syndrome.
Nongenomic actions of neurosteroid pregnenolone and its metabolites.
Intestinal Interleukin-17 Receptor Signaling Mediates Reciprocal Control of the Gut Microbiota and Autoimmune Inflammation.
Kappa opioid receptor activation alleviates experimental autoimmune encephalomyelitis and promotes oligodendrocyte-mediated remyelination.
Role of Subventricular Zone Derived Neural Precursor Cells in the Therapy of Experimental Autoimmune Encephalomyelitis.
Grey matter involvement by focal cervical spinal cord lesions is associated with progressive multiple sclerosis.
Phosphodiesterase-5 inhibition promotes remyelination by MCP-1/CCR-2 and MMP-9 regulation in a cuprizone-induced demyelination model.
The ideal healthcare: priorities of people with chronic conditions and their carers.
Anti-CCP Antibody Levels Are Not Associated with MS: Results from a Case-Control Study.
Inhibition of UCH-L1 in oligodendroglial cells results in microtubule stabilization and prevents α-synuclein aggregate formation by activating the autophagic pathway: implications for multiple system atrophy.
Cardiovascular effects of fingolimod: Relevance, detection and approach.
Brain functional plasticity at rest and during action in multiple sclerosis patients.
PDGF is Required for Remyelination-Promoting IgM Stimulation of Oligodendrocyte Progenitor Cell Proliferation.
Low myo-inositol indicating astrocytic damage in a case series of NMO.
Therapeutic Cleavage of Anti-Aquaporin-4 Autoantibody in Neuromyelitis Optica by an Igg-Selective Proteinase.
Risk of multiple sclerosis after a first demyelinating syndrome in an Australian Paediatric cohort: clinical, radiological features and application of the McDonald 2010 MRI criteria.
Regulatory genomic regions active in immune cell types explain a large proportion of the genetic risk of multiple sclerosis.
Heterogeneity of Multiple Sclerosis Lesions in Multislice Myelin Water Imaging.
Toxicity of cuprizone a Cu(2+) chelating agent on isolated mouse brain mitochondria: a justification for demyelination and subsequent behavioral dysfunction.
Increased activation of the epidermal growth factor receptor in transgenic mice overexpressing epigen causes peripheral neuropathy.
A new CSF1R mutation presenting with an extensive white matter lesion mimicking primary progressive multiple sclerosis.
Multiple sclerosis rehabilitation.
Charcot-Marie-Tooth disease: frequency of genetic subtypes and guidelines for genetic testing.

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