Disease | pulmonary fibrosis |
Phenotype | C0032285|pneumonitis |
Sentences | 7 |
PubMedID- 22778574 | Chest ct revealed pulmonary fibrosis consistent with typical interstitial pneumonitis (uip pattern) showing reticular opacity at the subpleural area in both lungs, especially in the right lower lobe. |
PubMedID- 20861649 | Background: chronic hypersensitivity pneumonitis (hp) can lead to irreversible pulmonary fibrosis. |
PubMedID- 24429272 | Chronic hypersensitivity pneumonitis in patients diagnosed with idiopathic pulmonary fibrosis: a prospective case-cohort study. |
PubMedID- 25889053 | Specifically, kk/hij, c57bl/6j, 129s1/svimj mice all had significant pulmonary fibrosis, with pneumonitis, when in distress and mice of the c3h/hej, a/j and akr/j strains succumbed with pneumonitis and no fibrosis. |
PubMedID- 20882179 | By distinction to drug-induced pulmonary pneumonitis that may lead to pulmonary fibrosis, ncpe can be reversed upon prompt recognition, following immediate discontinuation of the offensive drug and start of intensive supportive treatment although fatalities have been reported. |
PubMedID- 20855643 | The pathogenesis of chronic hypersensitivity pneumonitis in common with idiopathic pulmonary fibrosis: expression of apoptotic markers. |
PubMedID- 22037258 | A role for the highly inflammatory il-17 has been implicated in human asthma (39, 42), copd (43), experimental hypersensitivity pneumonitis (44), murine models of pulmonary fibrosis (11), and all autoimmune diseases that have been tested for its presence (45). |
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