Multiplex protein profiling of bronchoalveolar lavage in idiopathic pulmonary fibrosis and hypersensitivity pneumonitis

CONTEXT: Idiopathic pulmonary fibrosis (IPF) and chronic hypersensitivity pneumonitis (HP) are diffuse parenchymal lung diseases characterized by a mixture of inflammation and fibrosis, leading to lung destruction and finally death. AIMS: The aim of this study was to compare different pathophysiolog...

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Hlavní autoři: Stijn, Willems, Verleden, Stijn E., Vanaudenaerde, Bart M., Marijke, Wynants, Christophe, Dooms, Jonas, Yserbyt, Jana, Somers, Verbeken, Eric K., Verleden, Geert M., Wuyts, Wim A.
Médium: Artigo
Jazyk:Inglês
Vydáno: Medknow Publications & Media Pvt Ltd 2013
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Original Article
On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC3573557/
https://ncbi.nlm.nih.gov/pubmed/23440593
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4103/1817-1737.105718
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