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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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| Autors principals: | , , |
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| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
BioMed Central
2012
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| Matèries: | |
| Accés en línia: | 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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