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The Diagnosis and Treatment of Idiopathic Pulmonary Fibrosis
BACKGROUND: Idiopathic pulmonary fibrosis (IPF) is the most common idiopathic interstitial disease of the lung and has the worst prognosis of all such diseases, with a median survival time of three to four years. Its prevalence is 2–29 per 100 000 persons and its incidence approximately 10 per 100 0...
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| Format: | Artigo |
| Langue: | Inglês |
| Publié: |
Deutscher Arzte Verlag
2013
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| Accès en ligne: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3928534/ https://ncbi.nlm.nih.gov/pubmed/24529303 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3238/arztebl.2013.0875 |
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