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Multiple sclerosis registries in Europe – An updated mapping survey

Published:October 03, 2018DOI:https://doi.org/10.1016/j.msard.2018.09.032

      Highlights

      • Nineteen questionnaires from European MS registries were analysed.
      • Aim and focus as well as number of patients and inclusion criteria vary considerably.
      • Most of the MS registries collect data within common general categories.
      • There are more pronounced differences regarding specific subcategories.
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