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Minimum Data Set for Cystic Fibrosis Registry: a Case Study in Iran
BACKGROUND: over the last 25 years several national registries of CF have been set up. Such systems can be very useful in providing an integrated resource for improving patient care and conducting research on the disease. Minimum Data Set is a common set of data items that should be used to collect...
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| Foilsithe in: | Acta Inform Med |
|---|---|
| Main Authors: | , , , , |
| Formáid: | Artigo |
| Teanga: | Inglês |
| Foilsithe: |
AVICENA, d.o.o., Sarajevo
2015
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| Ábhair: | |
| Rochtain Ar Líne: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4384873/ https://ncbi.nlm.nih.gov/pubmed/25870486 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.5455/aim.2015.23.18-21 |
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