PedAM
Pediatric Disease Annotations & Medicines
| Disease | collagen disease |
| Phenotype | C0034069|pulmonary fibrosis |
| Sentences | 7 |
| 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- 25665185 | The aim of our study is to determine the diagnostic value of lung ultrasound in the detection of interstitial pulmonary fibrosis in patients with a rheumatic disease. |
| 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- 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. |
| PubMedID- 23341836 | The other chronic lung diseases reported in death certificates included pulmonary fibrosis due to connective tissue disease in two cases, and one case each of cryptogenic fibrosing alveolitis, asbestosis and pneumoconiosis, respectively. |
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