Skip to main content
Multiple Sclerosis Discovery Forum
Inspiring Connections
Utility Navigation
Feedback
Newsletter
RSS
Twitter
User Top Menu
Welcome, guest
Log In
Join
Why Join?
Search form
Search
About Us
Overview
Who We Are
Contact
Fan Mail
How to Cite
News & Future Directions
New Findings
News Briefs
Podcasts
News Synthesis
Essays & Opinions
Blogs
Papers
Editors' Picks
Classic Papers
Archive
Forums
Discussions
Webinars
Professional Resources
Meetings & Events
Past Meetings
Funding Opportunities
Jobs
Member Directory
Bulletin Board
Useful Links
Research Resources
Data Visualizations
Clinical Trials - Public Availability of Results
World Map
MS trials baseline
NMO History
NMO Galaxy
Map of MS Prevalence
Progressive MS Authors Galaxy
Word Cloud
MSLine
Ongoing Clinical Trials in MS
MRI-Related Clinical Trials
RRMS and CIS
Immunopathogenesis of MS
The MS Galaxy
ARR in Placebo Groups
Symptoms Prevalence
Scientific Literature TreeMap
Clinical Trials in MS
Drug-Development Pipeline
Tissue Repositories
MSGene
Animal Models
Clinical Trials
Click Here to Support MSDF
You are here
Home
Most Viewed
Founder mutations in NDRG1 and HK1 genes are common causes of inherited neuropathies among Roma/Gypsies in Slovakia.
Delayed Recovery of Leg Fatigue Symptoms Following a Maximal Exercise Session in People With Multiple Sclerosis.
Pediatric Inflammatory Diseases. Part II: Acute Post-Infectious Immune Disorders.
Myelin damage due to local quantitative abnormalities in normal prion levels: evidence from subacute combined degeneration and multiple sclerosis.
Anti-myelin antibodies play an important role in the susceptibility to develop PLP-induced EAE.
Cost-utility analysis of disease-modifying drugs in relapsing-remitting multiple sclerosis in Iran.
HINT1 peptide/Hsp70 complex induces NK cell-dependent immunoregulation in a model of autoimmune demyelination.
How do we manage and treat a patient with multiple sclerosis at risk of tuberculosis?
Multiple sclerosis for nurse practitioners.
Alemtuzumab in the treatment of multiple sclerosis: key clinical trial results and considerations for use.
Blocking GluR2-GAPDH ameliorates experimental autoimmune encephalomyelitis.
Detecting deoxyhemoglobin in spinal cord vasculature of the experimental autoimmune encephalomyelitis mouse model of multiple sclerosis using susceptibility MRI and hyperoxygenation.
The choroid plexus is modulated by various peripheral stimuli: implications to diseases of the central nervous system.
Comment on "Fingolimod effects on left ventricular function in multiple sclerosis" Mult Scler 2015.
EphB3 receptors function as dependence receptors to mediate oligodendrocyte cell death following contusive spinal cord injury.
T1- Thresholds in Black Holes Increase Clinical-Radiological Correlation in Multiple Sclerosis Patients.
Levels and actions of neuroactive steroids in the nervous system under physiological and pathological conditions: Sex-specific features.
Expression of DNA methylation genes in secondary progressive multiple sclerosis.
Improving reporting of multiple sclerosis relapse.
Acute Disseminated Encephalomyelitis in Children and Adolescents: A Single Center Experience.
Decoding movement intent of patient with multiple sclerosis for the powered lower extremity exoskeleton.
Diabetes insipidus as a rare cause of acute cognitive impairment in multiple sclerosis.
Towards patient collaboration in cognitive assessment: Specificity, sensitivity, and incremental validity of self-report.
Interferon alpha association with neuromyelitis optica.
Polyreactive monoclonal autoantibodies in multiple sclerosis: functional selection from phage display library and characterization by deep sequencing analysis.
Pages
« first
‹ previous
…
576
577
578
579
580
581
582
583
584
…
next ›
last »