B1 Non-refereed article in a scientific journal
Multiple sclerosis registries in Europe - An updated mapping survey
Authors: A. Glaser, A. Stahmann, T. Meissner, P. Flachenecker, D. Horáková, P. Zaratin, G. Brichetto, M. Pugliatti, O. Rienhoff, S. Vukusic, A.C. de Giacomoni, M.A. Battaglia, W. Brola, H. Butzkueven, R. Casey, J. Drulovic, K. Eichstädt, K. Hellwig, P. Iaffaldano, E. Ioannidou, J. Kuhle, K. Lycke, M. Magyari, T. Malbaša, R. Middleton, K.M. Myhr, K. Notas, A. Orologas, S. Otero-Romero, T. Pekmezovic, J. Sastre-Garriga, P. Seeldrayers, M. Soilu-Hänninen, L. Stawiarz, M. Trojano, T. Ziemssen, J. Hillert, C. Thalheim
Publisher: ELSEVIER SCI LTD
Publication year: 2019
Journal: Multiple Sclerosis and Related Disorders
Journal name in source: MULTIPLE SCLEROSIS AND RELATED DISORDERS
Journal acronym: MULT SCLER RELAT DIS
Volume: 27
Issue: January 2019
First page : 171
Last page: 178
Number of pages: 8
ISSN: 2211-0348
DOI: 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.
