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Idiopathic pulmonary fibrosis (IPF) is a chronic lung disease characterised by progressive scarring (fibrosis) of the lungs which leads to respiratory failure This review aims at describing the multiple ways by which IPF impacts lung function.
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This page is a summary of: Physiology of the lung in idiopathic pulmonary fibrosis, European Respiratory Review, January 2018, European Respiratory Society (ERS),
DOI: 10.1183/16000617.0062-2017.
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