Abstract

Idiopathic pulmonary fibrosis (IPF) is an irreversible and progressive lung disease with limited life expectancy after diagnosis. Histopathological studies of IPF lungs reveal the typical “Usual Interstitial Pneumonia” (UIP) pattern,...

Full Text
Paper version not known

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call