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Most Viewed Papers
Gait Profile Score in multiple sclerosis patients with low disability.
Familial amyotrophic lateral sclerosis with an I104F mutation in the SOD1 gene: Multisystem degeneration with neurofilamentous aggregates and SOD1 inclusions.
Loss of Myelin Basic Protein Function Triggers Myelin Breakdown in Models of Demyelinating Diseases.
Relationship of Obesity With Gait and Balance in People With Multiple Sclerosis.
Molecular characterization of biotic and abiotic stress-responsive MAP kinase genes, IbMPK3 and IbMPK6, in sweetpotato.
Symptom Management and Lifestyle Modifications in Multiple Sclerosis.
Alemtuzumab treatment alters circulating innate immune cells in multiple sclerosis.
Glutamate signalling: A multifaceted modulator of oligodendrocyte lineage cells in health and disease.
Ubiquitination of RORγt at Lysine 446 Limits Th17 Differentiation by Controlling Coactivator Recruitment.
IL4I1 augments CNS remyelination and axonal protection by modulating T cell driven inflammation.
Age at onset and seizure frequency affect white matter diffusion coefficient in patients with mesial temporal lobe epilepsy.
[Endogenous retroviruses are associated with autoimmune diseases].
Decreased arylesterase activity of paraoxonase-1 (PON-1) might be a common denominator of neuroinflammatory and neurodegenerative diseases.
Automated multi-objective calibration of biological agent-based simulations.
Pseudo-Foster Kennedy Syndrome as a Rare Presentation of Vitamin B12 Deficiency.
Fampridine and quality of life in individuals with multiple sclerosis.
Erratum to: The PROMESA-protocol: progression rate of multiple system atrophy under EGCG supplementation as anti-aggregation-approach.
Mercy killing in neurology: The beginnings of neurology on screen (II).
Development of rheumatoid arthritis during treatment of multiple sclerosis with interferon beta 1-a. Coincidence of two conditions or a complication of treatment: A case report.
Rebound Syndrome in Multiple Sclerosis After Fingolimod Cessation.
The Effect of Dimethyl Fumarate on Cerebral Gray Matter Atrophy in Multiple Sclerosis.
Weighted-SAMGSR: combining significance analysis of microarray-gene set reduction algorithm with pathway topology-based weights to select relevant genes.
Analysis of multiple sclerosis patients with electrophysiological and structural tests.
Cellular mechanisms of adaptive myelination: bridging the gap between animal studies and human cognition.
[Effect of axonal developmental disorders in the corpus callosum on the neurological function after birth in septic neonatal rats].
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