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Challenges, facilitators and barriers to the adoption and use of a web-based national IRD registry: lessons learned from the IRD-PT registry
Rare disease registries increase research accessibility for patients, while providing clinicians/investigators with a coherent data ecosystem necessary to boost research and patient care. The IRD-PT registry is a national, web-based, interoperable registry for inherited retinal degenerations (IRDs)...
Autores principales: | Marques, João Pedro, Vaz-Pereira, Sara, Costa, José, Marta, Ana, Henriques, José, Silva, Rufino |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9419370/ https://www.ncbi.nlm.nih.gov/pubmed/36028864 http://dx.doi.org/10.1186/s13023-022-02489-1 |
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