Why the study?
Systematic recording of data into national MS registries is needed to optimize treatment and define the pathogenesis of multiple sclerosis.
Population
Patients with multiple sclerosis in Norway
Design
Registry and biobank for systematic collection of clinical, epidemiological data and biological samples
Key result
The Norwegian Multiple Sclerosis Registry and Biobank was established to systematically collect clinical, epidemiological, and biological data to facilitate research and improve MS health care.
Authors
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Registry enables systematic MS data collection for treatment optimization; leaves open whether it improves outcomes pending prospective analyses.
Describes the establishment and purpose of the Norwegian Multiple Sclerosis Registry and Biobank for facilitating research and improving healthcare in MS.
Myhr et al. (2015) studied Multiple sclerosis. Norwegian Multiple Sclerosis Registry and Biobank was evaluated. The Norwegian Multiple Sclerosis Registry and Biobank was established to systematically collect clinical, epidemiological, and biological data to facilitate research and improve MS health care.
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