Titlebook: Idiopathic Pulmonary Fibrosis; A Comprehensive Clin Keith C. Meyer,Steven D. Nathan Book 2019Latest edition Springer Nature Switzerland AG

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2197-7372 de., Second Edition is an invaluable resource for clinicians who desire a deeper understanding of IPF in order to better help their patients..978-3-319-99975-3Series ISSN 2197-7372 Series E-ISSN 2197-7380

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Christopher S. King,Shambhu Aryal,Steven D. Nathan

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Michael P. Mohning,Jeffrey J. Swigris,Amy L. Olsontion efficiency, and is motivated by the ultimate goal of developing a high-power terahertz radiation source for time-domain terahertz spectroscopy and imaging systems..978-1-4614-2827-5978-1-4419-8198-1Series ISSN 2190-5053 Series E-ISSN 2190-5061

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Classification and Nomenclature of Interstitial Lung Disease,specific entity characterized by a usual interstitial pneumonia (UIP) histopathologic pattern that is not explained by the presence of lung involvement due to a connective tissue disorder (CTD), a non-IPF form of idiopathic interstitial pneumonia (IIP), or other causes of interstitial pneumonia such

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The Role of Immunity and Inflammation in IPF Pathogenesis,has been linked to vascular remodelling in the disease. Subsets of circulating monocytes, including fibrocytes and segregated-nucleus-containing atypical monocytes (SatM), have been identified that may facilitate progression of fibrosis, and apoptosis-resistant pulmonary macrophages have been shown

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