| Literature DB >> 31120376 |
Tomas Kalincik1, Helmut Butzkueven2.
Abstract
Over the last decade, clinical registries have significantly contributed to the pool of evidence that supports management decisions in patients with multiple sclerosis. Being the largest international registry of multiple sclerosis and neuroimmunological disorders, MSBase collects demographic, clinical and limited paraclinical information from patients managed in different regions and under various circumstances. In this review, we will provide an overview of its published output, with focus on the information with impact on the management of multiple sclerosis.Entities:
Keywords: MSBase; Observational data; registry; relapses; therapy
Mesh:
Year: 2019 PMID: 31120376 DOI: 10.1177/1352458519848965
Source DB: PubMed Journal: Mult Scler ISSN: 1352-4585 Impact factor: 6.312