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- W3025997144 endingPage "104025" @default.
- W3025997144 startingPage "104025" @default.
- W3025997144 abstract "Idiopathic pulmonary fibrosis (IPF) is a chronic and devastating disease of unknown etiology, characterized by irreversible morphological changes, ultimately leading to lung fibrosis and death. In recent years, significant progress has been achieved in understanding the pathogenesis of IPF. Moreover, we assisted to the conceptual change of the pathogenic hypothesis that currently considers IPF as a primarily fibrotic driven disease. However, despite the undeniable progress, the diagnosis of IPF remains still very complex requiring the presence of a team of experts to achieve the highest level of diagnostic confidence. The advent of antifibrotics has radically changed the treatment landscape of IPF and new promising drugs are currently under evaluation. Furthermore, a more extensive use of non-pharmacological treatments has also to be encouraged in all patients both to reduce symptoms and improve quality of life." @default.
- W3025997144 created "2020-05-21" @default.
- W3025997144 creator A5006969715 @default.
- W3025997144 creator A5008942733 @default.
- W3025997144 creator A5012539336 @default.
- W3025997144 creator A5020173096 @default.
- W3025997144 date "2020-06-01" @default.
- W3025997144 modified "2023-09-30" @default.
- W3025997144 title "Evolution and treatment of idiopathic pulmonary fibrosis" @default.
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