Disease | vascular disease |
Phenotype | C0034069|lung fibrosis |
Sentences | 1 |
PubMedID- 23697753 | Assessment of the above panel of immunologic markers was performed at the following serial time points: 1) at time of diagnosis as a part of routine work-up in order to exclude collagen vascular diseases as a cause of lung fibrosis, and 2) at regular follow-up every 6 months or earlier than 6 months if clinical signs compatible with autoimmune disease (arthralgia, muscle weakness, dysphagia, raynaud’s phenomenon, photosensitivity) or disease exacerbation (dyspnea deterioration, hemoptysis, hematuria) emerged. |
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