Towards a better diagnosis of idiopathic pulmonary fibrosis
Idiopathic pulmonary fibrosis (IPF) is the most common of the idiopathic interstitial pneumonias, and poses significant clinical challenges. IPF diagnosis is based on clear-cut computed tomography (CT) and histopathological criteria, in an appropriate clinical context. The diagnostic criteria includ...
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| Format: | Artigo |
| Jezik: | Inglês |
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European Respiratory Society
2011-06-01
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| Serija: | European Respiratory Review |
| Teme: | |
| Online dostop: | http://err.ersjournals.com/content/20/120/108.full.pdf+html |
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