PedAM
Pediatric Disease Annotations & Medicines
| Disease | pulmonary fibrosis |
| Phenotype | C0011644|scleroderma |
| Sentences | 7 |
| PubMedID- 26027239 | [clinical value of surfactant protein d as a biomarker of pulmonary fibrosis in patients with scleroderma systematica in relation to the presence of gastroesophageal reflux]. |
| PubMedID- 25505696 | Ger disease (gerd) has been associated with ipf and with pulmonary fibrosis in patients with systemic sclerosis (scleroderma), and ger with aspiration may play a role in triggering and/or driving lung inflammation and fibrosis in ipf and scleroderma, and it has been linked to acute exacerbations in patients with ipf [15, 16]. |
| PubMedID- 26464848 | Lower ratios were demonstrated in scleroderma and in patients with idiopathic pulmonary fibrosis. |
| PubMedID- 21050542 | Objectives: to evaluate an improved quantitative lung fibrosis score based on a computer-aided diagnosis (cad) system that classifies ct pixels with the visual semi-quantitative pulmonary fibrosis score in patients with scleroderma-related interstitial lung disease (ssc-ild). |
| PubMedID- 23244779 | Study explored the association of gerd and pulmonary fibrosis in patients with scleroderma with and without pulmonary fibrosis. |
| PubMedID- 25279305 | A case of pulmonary fibrosis associated with rheumatoid arthritis, scleroderma sine scleroderma and anca associated vasculitis. |
| PubMedID- 21923916 | For example, anti-tgf-β has been successfully shown to reduce skin and pulmonary fibrosis in mice with sclerodermatous graft-versus-host disease, a mouse model of the systemic fibrotic condition scleroderma [235]. |
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