Cargando…
The Quality Evaluation of Rare Disease Registries—An Assessment of the Essential Features of a Disease Registry
Rare disease (RD) registries aim to promote data collection and sharing, and facilitate multidisciplinary collaboration with the overall aim of improving patient care. Recommendations relating to the minimum standards necessary to develop and maintain high quality registries are essential to ensure...
Autores principales: | Ali, Salma Rashid, Bryce, Jillian, Kodra, Yllka, Taruscio, Domenica, Persani, Luca, Ahmed, Syed Faisal |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8620980/ https://www.ncbi.nlm.nih.gov/pubmed/34831724 http://dx.doi.org/10.3390/ijerph182211968 |
Ejemplares similares
-
The EuRRECa Project as a Model for Data Access and Governance Policies for Rare Disease Registries That Collect Clinical Outcomes
por: Ali, Salma R., et al.
Publicado: (2020) -
Recommendations for Improving the Quality of Rare Disease Registries
por: Kodra, Yllka, et al.
Publicado: (2018) -
Reflections on the Importance of Cost of Illness Analysis in Rare Diseases: A Proposal
por: Armeni, Patrizio, et al.
Publicado: (2021) -
Primary Sclerosing Cholangitis: Burden of Disease and Mortality Using Data from the National Rare Diseases Registry in Italy
por: Carbone, Marco, et al.
Publicado: (2020) -
The Occurrence of 275 Rare Diseases and 47 Rare Disease Groups in Italy. Results from the National Registry of Rare Diseases
por: Taruscio, Domenica, et al.
Publicado: (2018)