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Idiopathic pulmonary fibrosis: Early detection and referral
Idiopathic pulmonary fibrosis (IPF), a devastating progressive interstitial lung disease (ILD) with no known cause or cure, is the most common and deadly of the idiopathic interstitial pneumonias. With a median survival of 3–5 years following diagnosis, IPF is characterized by a progressive decline...
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| 出版年: | Respir Med |
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| 主要な著者: | , |
| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
2014
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| 主題: | |
| オンライン･アクセス: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4785031/ https://ncbi.nlm.nih.gov/pubmed/24746629 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.rmed.2014.03.008 |
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