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Idiopathic Pulmonary Fibrosis

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Cover of 'Idiopathic Pulmonary Fibrosis'

Table of Contents

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    Book Overview
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    Chapter 1 Classification and Nomenclature of Interstitial Lung Disease
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    Chapter 2 Idiopathic Pulmonary Fibrosis: The Epidemiology and Natural History of Disease
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    Chapter 3 Histopathology of IPF and Related Disorders
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    Chapter 4 Imaging of Idiopathic Pulmonary Fibrosis
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    Chapter 5 Pulmonary Function Tests in Idiopathic Pulmonary Fibrosis
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    Chapter 6 The Role of Immunity and Inflammation in IPF Pathogenesis
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    Chapter 7 Mechanisms of Fibrosis in IPF
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    Chapter 8 Genetics of Pulmonary Fibrosis
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    Chapter 9 Evolving Genomics of Pulmonary Fibrosis
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    Chapter 10 Biomarkers in Idiopathic Pulmonary Fibrosis
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    Chapter 11 Idiopathic Pulmonary Fibrosis: Phenotypes and Comorbidities
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    Chapter 12 The Keys to Making a Confident Diagnosis of IPF
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    Chapter 13 Pharmacologic Treatment of IPF
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    Chapter 14 Mimics of Idiopathic Pulmonary Fibrosis
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    Chapter 15 Gastroesophageal Reflux and IPF
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    Chapter 16 The Role of Pulmonary Rehabilitation and Supplemental Oxygen Therapy in the Treatment of Patients with Idiopathic Pulmonary Fibrosis
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    Chapter 17 Acute Exacerbation of Idiopathic Pulmonary Fibrosis
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    Chapter 18 Lung Transplantation for Idiopathic Pulmonary Fibrosis
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    Chapter 19 Clinical Trials in IPF: What Are the Best Endpoints?
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    Chapter 20 Future Directions for IPF Research
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Title
Idiopathic Pulmonary Fibrosis
Published by
Springer International Publishing, January 2019
DOI 10.1007/978-3-319-99975-3
ISBNs
978-3-31-999974-6, 978-3-31-999975-3
Editors

Keith C. Meyer, Steven D. Nathan

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