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Most Viewed
Characteristics of Geriatric Patients Diagnosed With Multiple Sclerosis Taking Disease Modifying Agents In The United States.
Novel antiepileptic drug lacosamide exerts neuroprotective effects by decreasing glial activation in the hippocampus of a gerbil model of ischemic stroke.
Pre-Existing Mature Oligodendrocytes Do Not Contribute to Remyelination following Toxin-Induced Spinal Cord Demyelination.
Cerebral venous thrombosis after high dose steroid in multiple sclerosis: a case report.
Anti-Aquaporin-1 Autoantibodies in Patients with Neuromyelitis Optica Spectrum Disorders.
Multiple sclerosis: IL-12p40-an early biomarker for multiple sclerosis?
Inner Nuclear Layer Thickening Is Inversley Proportional to Retinal Ganglion Cell Loss in Optic Neuritis.
A case of neuromyelitis optica spectrum disorder associated with a limited cutaneous systemic sclerosis and Sjögren syndrome.
Evaluation of gelatinases and IL-6 in the cerebrospinal fluid of patients with optic neuritis, multiple sclerosis and other inflammatory neurological diseases.
Interhemispheric cooperation in global-local visual processing in pediatric multiple sclerosis.
TGF-beta1 regulates human brain pericyte inflammatory processes involved in neurovasculature function.
▼Teriflunomide for multiple sclerosis.
Lymphocytic hypophysitis associated with pediatric multiple sclerosis.
Signal transduction and epigenetic mechanisms in the control of microglia activation during neuroinflammation.
Perception of muscular effort during dynamic elbow extension in multiple sclerosis.
Microglia regulate hippocampal neurogenesis during chronic neurodegeneration.
Influence of the LILRA3 Deletion on Multiple Sclerosis Risk: Original Data and Meta-Analysis.
A simple procedure for the extraction of DNA from long-term formalin-preserved brain tissues for the detection of EBV by PCR.
A study of retinal parameters measured by optical coherence tomography in patients with multiple sclerosis.
What lies beneath grey matter atrophy in multiple sclerosis?
Short-term effects of prolonged fasting on multiple sclerosis.
Mosaicism for GJB1 mutation causes milder Charcot-Marie-Tooth X1 phenotype in a heterozygous man than in a manifesting heterozygous woman.
Neurovascular unit dysfunction with blood-brain barrier hyperpermeability contributes to major depressive disorder: a review of clinical and experimental evidence.
In vivo dentate nucleus MRI relaxometry correlates with previous administration of Gadolinium-based contrast agents.
Can we prevent or treat multiple sclerosis by individualised vitamin D supply?
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