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Measuring what matters to rare disease patients – reflections on the work by the IRDiRC taskforce on patient-centered outcome measures

Abstract Our ability to evaluate outcomes which genuinely reflect patients’ unmet needs, hopes and concerns is of pivotal importance. However, much current clinical research and practice falls short of this objective by selecting outcome measures which do not capture patient value to the fullest. In...

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Detalhes bibliográficos
Principais autores: Thomas Morel, Stefan J. Cano
Formato: Artigo
Idioma:Inglês
Publicado em: BMC 2017-11-01
coleção:Orphanet Journal of Rare Diseases
Assuntos:
Acesso em linha:http://link.springer.com/article/10.1186/s13023-017-0718-x
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