The Swiss Multiple Sclerosis Registry (SMSR): study protocol of a participatory, nationwide registry to promote epidemiological and patient-centered MS research

by 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
Published 2018-08-01

60/30: 60% of the Morbidity-Associated Multiple Sclerosis Disease Burden Comes From the 30% of Persons With Higher Impairments

by Marco Kaufmann, Milo Alan Puhan, Anke Salmen, Christian P. Kamm, Christian P. Kamm, Zina-Mary Manjaly, Zina-Mary Manjaly, Pasquale Calabrese, Sven Schippling, Sven Schippling, Stefanie Müller, Jens Kuhle, Caroline Pot, Claudio Gobbi, Claudio Gobbi, Nina Steinemann, Viktor von Wyl, Swiss Multiple Sclerosis Registry (SMSR)
Published 2020-03-01