Abstract
Idiopathic pulmonary fibrosis (IPF) is a common form of interstitial lung disease and usually results in progressive respiratory insufficiency and death. Steady progress has been made in understanding the pathogenesis of IPF and multiple clinical trials are ongoing, but effective therapy remains elusive.
Original language | English (US) |
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Article number | 28 |
Journal | F1000 Medicine Reports |
Volume | 2 |
Issue number | 1 |
DOIs | |
State | Published - Apr 12 2010 |
ASJC Scopus subject areas
- Medicine(all)