Multiple Sclerosis Discovery Forum

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Mitochondrial dysfunctions in 7-ketocholesterol-treated 158N oligodendrocytes without or with α-tocopherol: Impacts on the cellular profil of tricarboxylic cycle-associated organic acids, long chain saturated and unsaturated fatty acids, oxysterols, chol
Editorial: Glial Cells: Managers of Neuro-Immunity.
Allelic imbalance of multiple sclerosis susceptibility genes IKZF3 and IQGAP1 in human peripheral blood.
Label free analysis of human cerebrospinal fluid addressing various normalization strategies and revealing protein groups affected by multiple sclerosis.
Neuroprotective effect of melatonin in experimental optic neuritis in rats.
Development of a Short Version of MSQOL-54 Using Factor Analysis and Item Response Theory.
Estrogen treatment of experimental autoimmune encephalomyelitis requires E2 receptor positive B cells that upregulate PD-1 on CD4(+) Foxp3(+) Treg cells.
Multiple sclerosis: Fatigue-a warning sign for multiple sclerosis?
[Semaphorin 4 in multiple sclerosis].
The Emerging Role of MitomiRs in the Pathophysiology of Human Disease.
The BICAMS Battery for Assessment of Lithuanian-Speaking Multiple Sclerosis Patients: Relationship with Age, Education, Disease Disability, and Duration.
CCRL2 regulates M1/M2 polarization during EAE recovery phase.
Nurse-led clinics for patients with chronic diseases in hospital and transmural care organizations.
Correction: Treatment with Vitamin D/MOG Association Suppresses Experimental Autoimmune Encephalomyelitis.
Randomized phase 1b trial of MOR103, a human antibody to GM-CSF, in multiple sclerosis.
Increased activation of the epidermal growth factor receptor in transgenic mice overexpressing epigen causes peripheral neuropathy.
Influence of multiple sclerosis, age and degree of disability, in the position of the contrast sensitivity curve peak.
More on JC viremia in natalizumab-treated patients with multiple sclerosis.
Erythrocytes' antioxidative capacity as a potential marker of oxidative stress intensity in neuroinflammation.
Charcot-Marie-Tooth disease: frequency of genetic subtypes and guidelines for genetic testing.
A Novel MPZ Gene Mutation in Exon 2 Causing Late-Onset Demyelinating Charcot-Marie-Tooth Disease.
Combining Double Fluorescence In Situ Hybridization with Immunolabelling for Detection of the Expression of Three Genes in Mouse Brain Sections.
Combination therapy with lenalidomide and nanoceria ameliorates CNS autoimmunity.
Case report of transverse myelitis in a patient receiving etanercept for rheumatoid arthritis.
Interferon-β therapy and risk of thrombocytopenia in multiple sclerosis patients.

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