Useful resources |
Immunomodulatory agents for idiopathic pulmonary fibrosis (Cochrane Review) ABSTRACT Background: Idiopathic Pulmonary Fibrosis (IPF) or Usual Interstitial Pneumonia (UIP) is a form of chronic fibrosing interstitial pneumonia of unknown aetiology, with progressively deteriorating respiratory function and ultimately death from respiratory failure. . . . |
Full article: The full article is available on Wiley InterScience at http://www.thecochranelibrary.com |