Idiopathic pulmonary fibrosis (IPF): Diagnostic routes using novel biomarkers
Idiopathic pulmonary fibrosis (IPF) diagnosis is still the diagnosis of exclusion. Differentiating from other forms of interstitial lung diseases (ILDs) is essential, given the various therapeutic approaches. The IPF course is now unpredictable for individual patients, although some genetic factors...
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| Hlavní autoři: | , , , , |
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| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
Elsevier
2024-08-01
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| Edice: | Biomedical Journal |
| Témata: | |
| On-line přístup: | http://www.sciencedirect.com/science/article/pii/S2319417024000325 |
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