Article
A novel protein signature from plasma extracellular vesicles for non-invasive differential diagnosis of idiopathic pulmonary fibrosis
2021-05-14
Abstract excerpt
<h4>Background</h4> Idiopathic pulmonary fibrosis (IPF) is a fibrosing interstitial pneumonia of unknown etiology often leading to respiratory failure. Over half of IPF patients present with discordant features of usual interstitial pneumonia on high-resolution computed tomography at diagnosis which warrants surgical lung biopsy to exclude the possibility of other interstitial lung diseases (ILDs). Therefore, ther...
Topics
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- COVID-19 Clinical Research Studies
- Extracellular vesicles in disease
- Interstitial Lung Diseases and Idiopathic Pulmonary Fibrosis
- Long-Term Effects of COVID-19
- Medical Imaging and Pathology Studies
- MicroRNA in disease regulation
- Pulmonary Hypertension Research and Treatments
- SARS-CoV-2 and COVID-19 Research
Identifiers and source
- Literature Corpus work
- 512f0034-2cd6-52f4-a9af-c65754c9701a
- DOI
- 10.1101/2021.05.07.21256811
