Multiple Sclerosis Discovery Forum

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Bilateral optic neuritis in a boy - More than the eyes.
Amelioration of EAE by a cryptic epitope of myelin oligodendrocyte glycoprotein.
[Melatonin as an inducing factor for multiple sclerosis].
Ionotropic glutamate receptor expression in human white matter.
White matter correlates of episodic memory encoding and retrieval in schizophrenia.
Quantification of Gait Abnormalities in Healthy-Looking Multiple Sclerosis Patients (with Expanded Disability Status Scale 0-1.5).
The influence of gut-derived CD39 regulatory T cells in CNS demyelinating disease.
Myelin Basic Protein Regulates Primitive and Definitive Neural Stem Cell Proliferation from the Adult Spinal Cord.
Coping with multiple sclerosis-the role of social support.
Psychosocial difficulties of individuals with multiple sclerosis: the PARADISE-24 questionnaire.
Glucocorticoid receptor haplotypes conferring increased sensitivity (BclI and N363S) are associated with faster progression of multiple sclerosis.
The Inflammatory Role of Platelets: Translational Insights from Experimental Studies of Autoimmune Disorders.
Vitamin D and Alzheimer's Disease: Neurocognition to Therapeutics.
The Adaptor Protein Rai/ShcC Promotes Astrocyte-Dependent Inflammation during Experimental Autoimmune Encephalomyelitis.
The contribution of neutrophils to CNS autoimmunity.
The Experience of Men Caring for a Partner With Multiple Sclerosis.
Influence of a low dose of silver nanoparticles on cerebral myelin and behavior of adult rats.
B Cell Malignancies Frequently Target the Autoreactive B Cell Repertoire.
Study design of PANGAEA 2.0, a non-interventional study on RRMS patients to be switched to fingolimod.
Perspiration Functions in Different Ethnic, Age, and Sex Populations: Modification of Sudomotor Function.
Prevalence of multiple sclerosis in Health District III, Murcia, Spain.
CSF β-amyloid as a putative biomarker of disease progression in multiple sclerosis.
Case-Control Studies Are Not Familial Studies.
[A treatment of neuromyelitis optica (Devic's disease) during pregnancy].
Gitelman syndrome, familial seizures, and demyelinating neuropathy: Rare association may be due to sodium potassium cotransporter genes.

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