Multiple Sclerosis Discovery Forum

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Most Viewed Papers

Functioning assessment vs. conventional medical assessment: a comparative study on health professionals' clinical decision-making and the fit with patient's own perspective of health.
MOG transmembrane and cytoplasmic domains contain highly stimulatory T-cell epitopes in MS.
Wheelchair design for people with neuromuscular disability.
[(18)F]-fluorodeoxyglucose-positron emission tomography in patients with active myelopathy.
Switching Therapies in Multiple Sclerosis.
A longitudinal study of cortical grey matter lesion subtypes in relapse-onset multiple sclerosis.
Gender influence on schizophrenia-relevant abnormalities in a cuprizone demyelination model.
Abnormal distribution of AQP5 in labial salivary glands is associated with poor saliva secretion in patients with Sjögren's syndrome including neuromyelitis optica complicated patients.
Clinical neurophysiology of multiple sclerosis.
Expanding spectrum of neurologic manifestations in patients with NLRP3 low-penetrance mutations.
TLR2 and TLR4 in Autoimmune Diseases: a Comprehensive Review.
Antibodies to MOG have a demyelination phenotype and affect oligodendrocyte cytoskeleton.
Cortical lesions in multiple sclerosis: inflammation versus neurodegeneration.
Level of mobility limitations and falls status in persons with multiple sclerosis.
VIP and PACAP: Neuropeptide modulators of CNS inflammation, injury, and repair.
The Promoter SNP, but not the Alternative Splicing SNP, is Linked to Multiple Sclerosis Among Jordanian Patients.
AKP-11 - A Novel S1P1 Agonist with Favorable Safety Profile Attenuates Experimental Autoimmune Encephalomyelitis in Rat Model of Multiple Sclerosis.
Clinical association of intrathecal and mirrored oligoclonal bands in paediatric neurology.
Analytical performances of SPAPLUS® turbidimeter for the quantification of albumin and IgG in serum and cerebrospinal fluid.
Obturator neurolysis using 65% alcohol for adductor muscle spasticity.
Multimodal neurophysiological evaluation of primary progressive multiple sclerosis - An increasingly valid biomarker, with limits.
X-linked Charcot-Marie-Tooth disease type 6 (CMTX6) patients with a p.R158H mutation in the pyruvate dehydrogenase kinase isoenzyme 3 gene.
Synthesis and Evaluation of Fluorinated Fingolimod (FTY720) Analogues for Sphingosine-1-Phosphate Receptor Molecular Imaging by Positron Emission Tomography.
Disease-modifying drugs for multiple sclerosis in pregnancy: A systematic review.
Multiple sclerosis: Grey matter atrophy in the thoracic spinal cord is associated with disability in patients with multiple sclerosis.

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