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Prognosis and Follow-Up of Idiopathic Pulmonary Fibrosis
Idiopathic pulmonary fibrosis (IPF), a devastating progressive interstitial lung disease (ILD) with no known cause, 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 in lung...
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| Vydáno v: | Med Sci (Basel) |
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| Hlavní autoři: | , , , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
MDPI
2018
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6024649/ https://ncbi.nlm.nih.gov/pubmed/29904028 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3390/medsci6020051 |
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