Multiple Sclerosis Discovery Forum

Inspiring Connections

Most Viewed Papers

Working memory network dysfunction in relapse-onset multiple sclerosis phenotypes: A clinical-imaging evaluation.
Significant Functional Improvement in a Person with Multiple Sclerosis Utilizing Dynamic Neuromuscular Stabilization: 1333 June 2, 8: 00 AM - 8: 20 AM.
Zeb2 is essential for Schwann cell differentiation, myelination and nerve repair.
IL-10 Modulates Th17 Pathogenicity during Autoimmune Diseases.
Cutaneous and Mixed Nerve Silent Period Recordings in Symptomatic Paroxysmal Kinesigenic Dyskinesia.
Successful surgical treatment of scoliosis secondary to Guillain-Barré syndrome: Case report.
Dimethyl fumarate may still have a role in progressive multiple sclerosis.
A new approach to follow a single extracellular vesicle-cell interaction using optical tweezers.
Use of natalizumab in multiple sclerosis: current perspectives.
Parasites and immunotherapy: with or against?
Fampridine and quality of life in individuals with multiple sclerosis.
Refractory trigeminal neuralgia responsive to nabiximols in a patient with multiple sclerosis.
Eosinophilic gastroenteritis in a woman with multiple sclerosis on dimethyl fumarate.
Clinical Features of Patients with Multiple Sclerosis and Neuromyelitis Optica Spectrum Disorders.
Upregulation of CD4+T-Cell Derived MiR-223 in The Relapsing Phase of Multiple Sclerosis Patients.
Neuromyelitis optica spectrum disorder coinciding with hematological immune disease: A case report.
Women's experiences of menopause in an online MS cohort: A case series.
Improvement of neurological disorders in postmenopausal model rats by administration of royal jelly.
Rifampicin attenuates experimental autoimmune encephalomyelitis by inhibiting pathogenic Th17 cells responses.
Non-Gaussian Diffusion Imaging Shows Brain Myelin and Axonal Changes in Obstructive Sleep Apnea.
Mannose-binding Lectin Mediated Complement Pathway in Autoimmune Neurological Disorders.
Increased regional gray matter atrophy and enhanced functional connectivity in male multiple sclerosis patients.
Familial amyotrophic lateral sclerosis with an I104F mutation in the SOD1 gene: Multisystem degeneration with neurofilamentous aggregates and SOD1 inclusions.
New oral drugs for the treatment of multiple sclerosis.
Scattering the spotlight on microparticles.

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