The Minimum Data Set for Rare Diseases: Systematic Review
BackgroundThe 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 and...
Saved in:
Main Authors: | Filipe Andrade Bernardi (Author), Bibiana Mello de Oliveira (Author), Diego Bettiol Yamada (Author), Milena Artifon (Author), Amanda Maria Schmidt (Author), Victória Machado Scheibe (Author), Domingos Alves (Author), Têmis Maria Félix (Author) |
---|---|
Format: | Book |
Published: |
JMIR Publications,
2023-07-01T00:00:00Z.
|
Subjects: | |
Online Access: | Connect to this object online. |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Similar Items
-
Data Quality in Health Research: Integrative Literature Review
by: Filipe Andrade Bernardi, et al.
Published: (2023) -
Establishing a minimum data set for Parkinson's (PMDS) in Iran
by: Ahmad Chitsaz, et al.
Published: (2022) -
Avaliação nutricional e autopercepção corporal associada ao uso de suplementos de praticantes de musculação em municípios da Serra Gaúcha
by: Milena Artifon, et al.
Published: (2016) -
the Development of a Minimum Data Set (MDS) for dental implants registry
by: Roya Naemi, et al.
Published: (2023) -
Development of a minimum data set for cardiac electrophysiology study ablation
by: Hadi Kazemi-Arpanahi, et al.
Published: (2019)