| 書目名稱 | Idiopathic Pulmonary Fibrosis | | 副標題 | A Comprehensive Clin | | 編輯 | Keith C. Meyer,Steven D. Nathan | | 視頻video | http://file.papertrans.cn/462/461073/461073.mp4 | | 概述 | Fully updated information on diagnosis and management of IPF, including six new chapters.Includes new coverage of interstitial lung disease classification, biomarkers in IPF, new concepts in disease p | | 叢書名稱 | Respiratory Medicine | | 圖書封面 |  | | 描述 | .This book is a comprehensive guide to our current understanding of idiopathic pulmonary fibrosis (IPF), its disease pathogenesis, genetic underpinnings, diagnosis, and management. Since the first edition, many new developments have occurred in the understanding and management of this serious disease, revising our understanding of how it presents, manifests, and reacts to certain treatments. This second edition is fully updated with six new chapters by our team of international, expert authors. New topics include: classification of interstitial lung disease, pulmonary function tests in IPF, biomarkers, clinical phenotypes, mimics, and a discussion of clinical trials. Each chapter additionally includes a brief summary of ongoing research and potential future directions. .Idiopathic Pulmonary Fibrosis: A Comprehensive Clinical Guide., Second Edition is an invaluable resource for clinicians who desire a deeper understanding of IPF in order to better help their patients.. | | 出版日期 | Book 2019Latest edition | | 關鍵詞 | idiopathic pulmonary fibrosis; IPF; interstitial lung disease; pulmonary function test; lung transplanta | | 版次 | 2 | | doi | https://doi.org/10.1007/978-3-319-99975-3 | | isbn_ebook | 978-3-319-99975-3Series ISSN 2197-7372 Series E-ISSN 2197-7380 | | issn_series | 2197-7372 | | copyright | Springer Nature Switzerland AG 2019 |
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