Features of the clinical picture and quality of life in patients with idiopathic pulmonary fibrosis and hypersensitivity pneumonitis
Background. Idiopathic pulmonary fibrosis (IPF) and hypersensitivity pneumonitis (HP) are interstitial lung diseases with similar symptoms: dyspnea and cough, which determine disease severity and serve as prognostic markers. Aim. To compare clinical and functional characteristics and their dynami...
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| Principais autores: | , , , , , |
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| Formato: | Artigo |
| Idioma: | Russo |
| Publicado em: |
ZAO "Consilium Medicum"
2025-01-01
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| coleção: | Consilium Medicum |
| Assuntos: | |
| Acesso em linha: | https://consilium.orscience.ru/2075-1753/article/viewFile/678792/200410 |
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