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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Detalles Bibliográficos
Autores principales: Kalankesh, Leila R, Dastgiri, Saeed, Rafeey, Mandana, Rasouli, Narmin, Vahedi, Leila
Formato: Online Artículo Texto
Lenguaje:English
Publicado: AVICENA, d.o.o., Sarajevo 2015
Materias:
Original Paper
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4384873/
https://www.ncbi.nlm.nih.gov/pubmed/25870486
http://dx.doi.org/10.5455/aim.2015.23.18-21

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4384873/
https://www.ncbi.nlm.nih.gov/pubmed/25870486
http://dx.doi.org/10.5455/aim.2015.23.18-21

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