Idiopathic Pulmonary Fibrosis
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Since December, 2019, Wuhan, China, has… Expand The most common signs and symptoms of idiopathic pulmonary fibrosis are shortness of breath and a persistent dry, hacking cough… Expand BACKGROUND
In two of three phase 3 trials, pirfenidone, an oral antifibrotic therapy, reduced disease progression, as measured by… Expand BACKGROUND
Blockade of programmed death 1 (PD-1), an inhibitory receptor expressed by T cells, can overcome immune resistance. We… Expand This document is an international evidence-based guideline on the diagnosis and management of idiopathic pulmonary fibrosis, and… Expand BACKGROUND
Idiopathic pulmonary fibrosis is a progressive and fatal lung disease with inevitable loss of lung function. The… Expand Idiopathic pulmonary fibrosis is a specific form of chronic fibrosing interstitial pneumonia limited to the lung. Although its… Expand Many acute and chronic lung disorders with variable degrees of pulmonary inflammation and fibrosis are collectively referred to… Expand Background Pathologic Classification of Idiopathic Pulmonary Fibrosis UIP DIP/Respiratory Bronchiolitis Interstitial Lung Disease… Expand The role and limitations of retrospective investigations of factors possibly associated with the occurrence of a disease are… Expand