Cargando…
The Minimum Data Set for Rare Diseases: Systematic Review
BACKGROUND: The minimum data set (MDS) is a collection of data elements to be grouped using a standard approach to allow the use of data for clinical and research purposes. Health data are typically voluminous, complex, and sometimes too ambiguous to generate indicators that can provide knowledge an...
Autores principales: | Bernardi, Filipe Andrade, Mello de Oliveira, Bibiana, Bettiol Yamada, Diego, Artifon, Milena, Schmidt, Amanda Maria, Machado Scheibe, Victória, Alves, Domingos, Félix, Têmis Maria |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
JMIR Publications
2023
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10415943/ https://www.ncbi.nlm.nih.gov/pubmed/37498666 http://dx.doi.org/10.2196/44641 |
Ejemplares similares
-
Epidemiology of rare diseases in Brazil: protocol of the Brazilian Rare Diseases Network (RARAS-BRDN)
por: Félix, Têmis Maria, et al.
Publicado: (2022) -
Mapping, Infrastructure, and Data Analysis for the Brazilian Network of Rare Diseases: Protocol for the RARASnet Observational Cohort Study
por: Alves, Domingos, et al.
Publicado: (2021) -
Data Quality in Health Research: Integrative Literature Review
por: Bernardi, Filipe Andrade, et al.
Publicado: (2023) -
Availability of Genetic Tests in Public Health Services in Brazil: Data from the Brazilian Rare Diseases Network
por: de Oliveira, Bibiana Mello, et al.
Publicado: (2023) -
Ontology-Based Inference for Supporting Clinical Decisions in Mental Health
por: Yamada, Diego Bettiol, et al.
Publicado: (2020)