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Research priorities for rare neurological diseases: a representative view of patient representatives and healthcare professionals from the European Reference Network for Rare Neurological Diseases

Abstract Background Patient involvement in research increases the impact of research and the likelihood of adoption in clinical practice. A first step is to know which research themes are important for patients. We distributed a survey on research priorities to ERN-RND members, both patient represen...

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Principais autores: Annemarie E. M. Post, Thomas Klockgether, G. Bernhard Landwehrmeyer, Massimo Pandolfo, Astri Arnesen, Carola Reinhard, Holm Graessner
Format: Artigo
Jezik:Inglês
Izdano: BMC 2021-03-01
Serija:Orphanet Journal of Rare Diseases
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Online dostop:https://doi.org/10.1186/s13023-020-01641-z
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