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Continually improving standards of care: The UK Renal Registry as a translational public health tool
A disease registry uses observational study methods to collect defined data on patients with a particular condition for a predetermined purpose. By providing comprehensive standardised data on patients with kidney disease, renal registries aim to provide a ‘real world’ representation of practice pat...
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| Publicat a: | Pediatr Nephrol |
|---|---|
| Autors principals: | , , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
Springer Berlin Heidelberg
2017
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5799353/ https://ncbi.nlm.nih.gov/pubmed/28642999 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s00467-017-3688-2 |
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