Related Experiment Video
Updated: Apr 11, 2026
10:46
A Method of Trigonometric Modelling of Seasonal Variation Demonstrated with Multiple Sclerosis Relapse Data
Published on: December 9, 2015
11.2K
The Norwegian Multiple Sclerosis Registry and Biobank
K-M Myhr1,2, N Grytten2,3, Ø Torkildsen2,3
1Norwegian Multiple Sclerosis Registry and Biobank, Department of Neurology, Haukeland University Hospital, Bergen, Norway.
Acta Neurologica Scandinavica
|June 6, 2015
Summary
The Norwegian Multiple Sclerosis Registry and Biobank collects patient data to advance understanding of MS disease mechanisms and improve patient care. This resource facilitates research by providing access to clinical and biological information for scientists.
Area of Science:
- Neurology
- Epidemiology
- Biomedical Research
Background:
- Multiple sclerosis (MS) is a chronic central nervous system inflammatory disease with complex pathogenesis.
- Disease-modifying therapies offer benefits, necessitating optimized treatment strategies.
- Systematic data collection is crucial for advancing MS research and care.
Purpose of the Study:
- To establish and describe the Norwegian Multiple Sclerosis Registry and Biobank.
- To facilitate research into MS pathogenesis and treatment optimization.
- To provide researchers with access to clinical and biological data.
Main Methods:
- Systematic collection of clinical and epidemiological data from MS patients.
- Informed consent obtained from individual patients.
- Recording of data by treating neurologists.
- Collection of biological samples for biobanking.
Main Results:
- The Norwegian MS Registry and Biobank has been established for systematic data collection.
- Access to data and biological samples is available to researchers upon application.
- The registry facilitates collaborative efforts between patients and healthcare professionals.
Conclusions:
- The Norwegian MS Registry and Biobank is a valuable resource for MS research.
- Enhanced understanding of MS disease mechanisms can be achieved through registry data.
- Improved healthcare for MS patients is a key objective facilitated by the registry.
