Hasil Pencarian - the Swiss Multiple Sclerosis Registry

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  1. 1
    A digitally facilitated citizen-science driven approach accelerates participant recruitment and increases study population diversity

    A digitally facilitated citizen-science driven approach accelerates participant recruitment and increases study population diversity oleh Milo A. Puhan, Nina Steinemann, Christian P Kamm, Stefanie Müller, Jens Kuhle, Roland Kurmann, Pasquale Calabrese, Jürg Kesselring, Viktor von Wyl, on behalf of the Swiss Multiple Sclerosis Registry (SMSR)

    Diterbitkan 2018-05-01
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  2. 2
    The Swiss Multiple Sclerosis Registry (SMSR): study protocol of a participatory, nationwide registry to promote epidemiological and patient-centered MS research

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

    Diterbitkan 2018-08-01
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  3. 3
    60/30: 60% of the Morbidity-Associated Multiple Sclerosis Disease Burden Comes From the 30% of Persons With Higher Impairments

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

    Diterbitkan 2020-03-01
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