PedAM
Pediatric Disease Annotations & Medicines
| Disease | pulmonary fibrosis |
| Phenotype | C0009782|connective tissue disease |
| Sentences | 5 |
| PubMedID- 24791173 | [789] only recently has it been considered a valid method for the assessment of interstitial pulmonary fibrosis in patients with connective tissue diseases[1011] compared with hrct as the concurrent gold standard. |
| PubMedID- 23997057 | Pulmonary hypertension (ph) is a common complication of interstitial lung diseases (ilds), particularly in idiopathic pulmonary fibrosis and ild associated with connective tissue disease. |
| PubMedID- 25307273 | Background and aims: information regarding autoimmune symptoms that do not meet the diagnostic criteria for connective tissue disease in patients with idiopathic pulmonary fibrosis (ipf) is limited. |
| PubMedID- 23247773 | Idiopathic pulmonary fibrosis (ipf), fibrosis associated with connective tissue disease, asbestosis, end-stage sarcoidosis or chronic hypersensitivity pneumonitis (hp) may present with lower zone, subpleural reticular pattern associated with honeycombing. |
| PubMedID- 21924888 | Does the presence of connective tissue disease modify survival in patients with pulmonary fibrosis. |
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