Cargando…
Swedish guidelines for registry-based randomized clinical trials
During the last decade Sweden has invested in a national infrastructure for collection of structured clinical data in the form of healthcare registries (in Sweden known as Kvalitetsregister). These data can be combined with other public data using the national personal identifiers that are issued to...
Autores principales: | Nyberg, Karl, Hedman, Peter |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Taylor & Francis
2019
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6450469/ https://www.ncbi.nlm.nih.gov/pubmed/30724666 http://dx.doi.org/10.1080/03009734.2018.1550453 |
Ejemplares similares
-
Predictors of severe COVID-19 in a registry-based Swedish cohort of patients with COPD
por: Stridsman, Caroline, et al.
Publicado: (2021) -
The swedish paediatric JIA-registry
por: Magnusson, Bo
Publicado: (2014) -
Obstetric Thromboprophylaxis: The Swedish Guidelines
por: Lindqvist, Pelle G., et al.
Publicado: (2011) -
The Swedish MS registry – clinical support tool and scientific resource
por: Hillert, J, et al.
Publicado: (2015) -
An Overview of Guidelines for Supplemental Feeding of Infants in Swedish Maternity Clinics
por: Kerstis, Birgitta, et al.
Publicado: (2021)