Idiopathic pulmonary fibrosis (IPF) is a progressive and irreversible fibrosing interstitial
pneumonia of unknown aetiology that usually leads to respiratory failure and death within 5 …

Idiopathic pulmonary fibrosis (IPF) is a unique type of chronic fibrosing lung disease of
unknown etiology. The sequence of the pathogenic mechanisms is unknown, but the …

Idiopathic pulmonary fibrosis (IPF) is a chronic, progressive, and usually fatal pulmonary
disease for which there are no proven drug therapies. Anti-inflammatory and …

Idiopathic pulmonary fibrosis (IPF) is a progressive scarring disease of the lung with poor
survival. The incidence and mortality of IPF are rising, but treatment remains limited …

Idiopathic pulmonary fibrosis (IPF) is a fibrosing interstitial lung disease associated with
aging that is characterized by the histopathological pattern of usual interstitial pneumonia …

Idiopathic pulmonary fibrosis (IPF), also termed cryptogenic fibrosing alveolitis, is a
clinicopathological syndrome characterised by cough, exertional dyspneoa, basilar crackles …

Idiopathic pulmonary fibrosis is a chronic and usually progressive lung disorder of unknown
etiology. A growing body of evidence suggests that, in contrast to other interstitial lung …

Abstract Background and Aim Idiopathic pulmonary fibrosis (IPF) is characterized by
hyperplasia of type II alveolar epithelial cells, aggregation of activated (myo) fibroblasts and …

Idiopathic pulmonary fibrosis (IPF) is the most common and lethal form of idiopathic
interstitial pneumonia. The disease is thought to arise following an aberrant reparative …

Numerous studies have been published investigating the pathologic alterations in various
interstitial pneumonias, particularly in idiopathic pulmonary fibrosis (IPF). However, the few …