The Swiss Multiple Sclerosis Registry (SMSR): study protocol of a participatory, nationwide registry to promote epidemiological and patient-centered MS research
Abstract Background Multiple sclerosis (MS) is one of the most frequently observed neurological conditions in Switzerland, but data sources for country-wide epidemiological trend monitoring are lacking. Moreover, while clinical and laboratory MS research are generally well established, there is a ga...
Main Authors: | Nina Steinemann, Jens Kuhle, Pasquale Calabrese, Jürg Kesselring, Giulio Disanto, Doron Merkler, Caroline Pot, Vladeta Ajdacic-Gross, Stephanie Rodgers, Milo Alan Puhan, Viktor von Wyl, the Swiss Multiple Sclerosis Registry |
---|---|
Format: | Article |
Language: | English |
Published: |
BMC
2018-08-01
|
Series: | BMC Neurology |
Subjects: | |
Online Access: | http://link.springer.com/article/10.1186/s12883-018-1118-0 |
Similar Items
-
A digitally facilitated citizen-science driven approach accelerates participant recruitment and increases study population diversity
by: Milo A. Puhan, et al.
Published: (2018-05-01) -
Emergency medicine training: is undergraduate training sufficient for the Swiss health-care system?
by: Swiss Medical Weekly
Published: (2009-07-01) -
Measuring the Coverage Bias in Landline Telephone Surveys by Comparison of Swiss Registry Data with Commercially Available Telephone Number Databases
by: Stefan Klug, et al.
Published: (2016-11-01) -
Swiss profiles [kasetvideo] /
by: Richardet, Claude
Published: (1991) -
The Effect of Depression on Health-Related Quality of Life Is Mediated by Fatigue in Persons with Multiple Sclerosis
by: Stephanie Rodgers, et al.
Published: (2021-06-01)