Idiopathic pulmonary fibrosis is defined as a chronic fibrosing interstitial pneumonia limited
to the lung, of unknown cause, with poor prognosis and few treatment options. In recent …

Idiopathic pulmonary fibrosis is a rare interstitial lung disease included in the Idiopathic
Interstitial Pneumonias group. Although several potential risk factors have been described, it …

Idiopathic pulmonary fibrosis is defined as chronic fibrosing interstitial pneumonia limited to
the lung, with poor prognosis. The incidence has been rising in recent years probably due to …

Idiopathic pulmonary fibrosis (IPF) is a specific type of fibrosing interstitial pneumonia of
unknown cause. It is usually chronic and progressive, tends to affect mainly adults over age …

Idiopathic pulmonary fibrosis is defined as a chronic progressive fibrosing interstitial
pneumonia of unknown etiology. There are intrinsic and extrinsic risk factors that could favor …

Idiopathic pulmonary fibrosis (IPF) is the most frequent chronic idiopathic interstitial
pneumonia in adults. The management of rare diseases in France has been organised by a …

Introduction Idiopathic pulmonary fibrosis (IPF) is a progressive, irreversible and frequently
fatal disease. Currently there are national and multinational registries in Europe, United …

Idiopathic pulmonary fibrosis (IPF) is the most prevalent of the idiopathic interstitial
pneumonias and its incidence seems to be increasing [1–4]. IPF is generally considered to …

This document is an international evidence-based guideline on the diagnosis and
management of idiopathic pulmonary fibrosis, and is a collaborative effort of the American …

Idiopathic pulmonary fibrosis (IPF) is a rare disease characterized by chronic, progressive,
and irreversible interstitial lung fibrosis of unknown cause [1, 2]. Main symptoms and signs …