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Most Viewed
An Observational Study of the Impact of Systemic B-cell Depletion on Cervicovaginal Mucosal Environment.
[Age-related aspects of multiple sclerosis].
Efficacy of Sativex® on pain, spasticity, and disability in patients with multiple sclerosis: A systematic review and meta-analysis.
Therapeutic effect of T-cell engager in two patients with autoimmune neuropathy.
Optic Nerve Lesion Volume, White Matter Hyperintensities, and Brain Volumetrics in Multiple Sclerosis: A Multi-Sequence MRI-Based Analysis.
Nonbrachial Plexopathy Diagnoses Seen in a Brachial Plexus Injury Specialty Clinic.
Disruption to TFEB signaling and autophagy in newly formed oligodendrocytes leads to aberrant generation of CNS myelin.
The genetic architecture of fibromyalgia across 2.5 million individuals.
A Structured Aerobic Exercise Program Increases Physical Activity in People With Parkinson's Disease: A Secondary Analysis of the CYCLE-II Trial.
Unmasking the invisible: Correlates and impact of cognitive complaints in MS.
An Exploratory Cross-Sectional Study of the Association Between Regular Cigarette Smoking and Level of Disability, Hand Dexterity, Cognitive Impairment, Fatigue, and Markers of Oxidative Stress in Male Patients With Relapsing-Remitting Multiple Sclerosis.
Corrigendum to "Sample size estimation for AQP4-IgG seropositive optic neuritis: retinal damage detection by optical coherence tomography".
High early mortality and contributing factors in seropositive neuromyelitis optica spectrum disorder at a tertiary hospital in Zambia.
[Disease associated with anti-myelin oligodendrocyte glycoprotein (MOGAD)].
[When Guillain-Barré syndrome is not monophasic: Distinguishing recurrent Guillain-Barré syndrome from acuteonset chronic inflammatory demyelinating polyneuropathy and nodopathies].
Reduced FOXP3 expression and its association with genetic ancestry in neuromyelitis Optica spectrum disorder: a Colombian cohort.
Long-term safety, tolerability, and efficacy of subcutaneous efgartigimod PH20 in generalized myasthenia gravis: final results from a phase 3 open-label extension study (ADAPT-SC+).
A Rare Case of Fatty Acid Hydroxylase-Associated Neurodegeneration in a Pakistani Boy With a Homozygous FA2H Variant.
Steroid Refractory and Plasma Exchange Partially Responsive Longitudinally Extensive Transverse Myelitis Due to Tumor Necrosis Factor-Alpha (Etanercept): A Case Report.
Co-administration of quercetin and NLRP3 inhibitor attenuates inflammation and oxidative stress in cuprizone-induced demyelination model.
Early Myelination Supports the Establishment of Consistent Handedness.
Diffusion-relaxation MRI as virtual histology: separable microstructural signatures of AD pathology in ex vivo human brain.
Autoimmune nodopathy associated with Sjögren's disease and nephrotic syndrome: a case report and literature review.
MS phenotypes should be abandoned in favour of a continuous disease spectrum model - 'Commentary'.
New Onset Myelin Oligodendrocyte Glycoprotein-Related Optic Neuritis During Peripartum Period.
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