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Specific Serum Markers of IPF: What Is the Significance of KL-6, SP-A, and SP-D?
Idiopathic pulmonary fibrosis (IPF) is defined as a specific form of chronic, progressive, fibrosing interstitial pneumonia of unknown cause. It is characterized by the progressive worsening of lung function and has a poor prognosis (median survival is approximately 3 years). However, the clinical c...
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| Publicado no: | Idiopathic Pulmonary Fibrosis |
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| Main Authors: | , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2015
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7120645/ https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/978-4-431-55582-7_5 |
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