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The care needs of patients with idiopathic pulmonary fibrosis and their carers (CaNoPy): results of a qualitative study
BACKGROUND: Idiopathic pulmonary fibrosis (IPF) is a chronic, fibrotic interstitial lung disease of unknown origin. It has a median survival of three years but a wide range in survival rate which is difficult to predict at the time of diagnosis. Specialist guidance promotes a patient centred approac...
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| Publicat a: | BMC Pulm Med |
|---|---|
| Autors principals: | , , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
BioMed Central
2015
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4670492/ https://ncbi.nlm.nih.gov/pubmed/26637194 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12890-015-0145-5 |
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