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    Should analyses of large, national palliative care data sets with patient reported outcomes (PROs) be restricted to services with high patient participation? A register-based study

    Should analyses of large, national palliative care data sets with patient reported outcomes (PROs) be restricted to services with high patient participation? A register-based study oleh Maiken Bang Hansen, Morten Aagaard Petersen, Lone Ross, Mogens Groenvold

    Diterbitkan 2020-06-01
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