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Aberrant innate immune sensing leads to the rapid progression of idiopathic pulmonary fibrosis
Novel approaches are needed to define subgroups of patients with Idiopathic pulmonary fibrosis (IPF) at risk for acute exacerbations and/or accelerated progression of this generally fatal disease. Progression of disease is an integral component of IPF with a median survival of 3 to 5 years. Converse...
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| Main Authors: | , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado: |
BioMed Central
2012
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| Assuntos: | |
| Acceso en liña: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3368762/ https://ncbi.nlm.nih.gov/pubmed/23259678 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1755-1536-5-S1-S3 |
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