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The RUDY study platform – a novel approach to patient driven research in rare musculoskeletal diseases
BACKGROUND: Research into rare diseases is becoming more common, with recognition of the significant diagnostic and therapeutic care gaps. Registries are considered a key research methodology to address rare diseases. This report describes the structure of the Rare UK Diseases Study (RUDY) platform...
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Pubblicato in: | Orphanet J Rare Dis |
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Autori principali: | , , , , , , , , , , , , , , , , , |
Natura: | Artigo |
Lingua: | Inglês |
Pubblicazione: |
BioMed Central
2016
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Soggetti: | |
Accesso online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5101709/ https://ncbi.nlm.nih.gov/pubmed/27825362 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s13023-016-0528-6 |
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