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Idiopathic Pulmonary Fibrosis and Lung Cancer: Mechanisms and Molecular Targets
Idiopathic pulmonary fibrosis (IPF) is the most common idiopathic interstitial pulmonary disease with a median survival of 2–4 years after diagnosis. A significant number of IPF patients have risk factors, such as a history of smoking or concomitant emphysema, both of which can predispose the patien...
| Autores principales: | , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
MDPI
2019
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| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6387034/ https://www.ncbi.nlm.nih.gov/pubmed/30704051 http://dx.doi.org/10.3390/ijms20030593 |