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Idiopathic Pulmonary Fibrosis: A Comprehensive Clinical Guide

Keith C. Meyer, Steven D. Nathan, editors
Format
EBook; Book; Online
Published
New York : Humana Press, 2014.
Language
English
Series
Respiratory Medicine
Respiratory Medicine (New York, N.Y.)
ISBN
9781627036825, 1627036822, 9781627036818
Access Restriction
Electronic access is available for UVA students, faculty, staff, and affiliates only. IP address verification required.
Summary
Idiopathic Pulmonary Fibrosis: A Comprehensive Clinical Guide delivers a concise review of our current understanding of disease pathogenesis and provides current evidence in the medical literature regarding its diagnosis and management. Each chapter includes key points and a summary aiming to update clinicians about various issues concerning the diagnosis and management of IPF. In addition to outlining the current state of knowledge, each chapter also provides a summary of ongoing research and identifies the needs for future research in the field. Idiopathic Pulmonary Fibrosis: A Comprehensive Clinical Guide is an important new text that provides its readers with a better understanding of the pathobiology and natural history of IPF as it continues to evolve.
Contents
  • Chapter 1: Idiopathic Pulmonary Fibrosis: A Historical Perspective
  • Chapter 2: Idiopathic Pulmonary Fibrosis: The Epidemiology and Natural History of Disease
  • Chapter 3: Histopathology of IPF and Related Disorders
  • Chapter 4: Imaging of Idiopathic Pulmonary Fibrosis
  • Chapter 5: The Keys to Making a Confident Diagnosis of IPF
  • Chapter 6: Pulmonary Function Tests in Idiopathic Pulmonary Fibrosis
  • Chapter 7: The Role of Adaptive Immunity in Idiopathic Pulmonary Fibrosis: Hiding in Plain Sight
  • Chapter 8: Mechanisms of Fibrosis in IPF
  • Chapter 9: The Emerging Genetics of Interstitial Lung Disease
  • Chapter 10: Idiopathic Pulmonary Fibrosis Phenotypes
  • Chapter 11: Idiopathic Interstitial Pneumonia and Connective Tissue Disease-Associated Interstitial Lung Disease: Similarities and Differences
  • Chapter 12: Aging and IPF: What Is the Link?
  • Chapter 13: Gastroesophageal Reflux and IPF
  • Chapter 14: Pharmacological Treatment of Idiopathic Pulmonary Fibrosis
  • Chapter 15: Recognizing and Treating Comorbidities of IPF
  • Chapter 16: The Role of Pulmonary Rehabilitation and Supplemental Oxygen Therapy in the Treatment of Patients with Idiopathic Pulmonary Fibrosis
  • Chapter 17: Acute Exacerbation of Idiopathic Pulmonary Fibrosis
  • Chapter 18: Lung Transplantation for Idiopathic Pulmonary Fibrosis
  • Chapter 19: Evolving Genomics of Pulmonary Fibrosis
  • Chapter 20: Idiopathic Pulmonary Fibrosis Clinical Trials: Evolving Concepts
  • Chapter 21: Future Directions in Basic and Clinical Science.
Description
1 online resource (xv, 451 pages) : illustrations (some color).
Notes
Includes bibliographical references and index.
Series Statement
Respiratory Medicine ; 9
Respiratory medicine (New York, N.Y.) 9
Copyright Not EvaluatedCopyright Not Evaluated
Technical Details
  • Access in Virgo Classic
  • Staff View

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    a| Chapter 1: Idiopathic Pulmonary Fibrosis: A Historical Perspective -- Chapter 2: Idiopathic Pulmonary Fibrosis: The Epidemiology and Natural History of Disease -- Chapter 3: Histopathology of IPF and Related Disorders -- Chapter 4: Imaging of Idiopathic Pulmonary Fibrosis -- Chapter 5: The Keys to Making a Confident Diagnosis of IPF -- Chapter 6: Pulmonary Function Tests in Idiopathic Pulmonary Fibrosis -- Chapter 7: The Role of Adaptive Immunity in Idiopathic Pulmonary Fibrosis: Hiding in Plain Sight -- Chapter 8: Mechanisms of Fibrosis in IPF -- Chapter 9: The Emerging Genetics of Interstitial Lung Disease -- Chapter 10: Idiopathic Pulmonary Fibrosis Phenotypes -- Chapter 11: Idiopathic Interstitial Pneumonia and Connective Tissue Disease-Associated Interstitial Lung Disease: Similarities and Differences -- Chapter 12: Aging and IPF: What Is the Link? -- Chapter 13: Gastroesophageal Reflux and IPF -- Chapter 14: Pharmacological Treatment of Idiopathic Pulmonary Fibrosis -- Chapter 15: Recognizing and Treating Comorbidities of IPF -- Chapter 16: The Role of Pulmonary Rehabilitation and Supplemental Oxygen Therapy in the Treatment of Patients with Idiopathic Pulmonary Fibrosis -- Chapter 17: Acute Exacerbation of Idiopathic Pulmonary Fibrosis -- Chapter 18: Lung Transplantation for Idiopathic Pulmonary Fibrosis -- Chapter 19: Evolving Genomics of Pulmonary Fibrosis -- Chapter 20: Idiopathic Pulmonary Fibrosis Clinical Trials: Evolving Concepts -- Chapter 21: Future Directions in Basic and Clinical Science.
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    a| Includes bibliographical references and index.
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    a| Idiopathic Pulmonary Fibrosis: A Comprehensive Clinical Guide delivers a concise review of our current understanding of disease pathogenesis and provides current evidence in the medical literature regarding its diagnosis and management. Each chapter includes key points and a summary aiming to update clinicians about various issues concerning the diagnosis and management of IPF. In addition to outlining the current state of knowledge, each chapter also provides a summary of ongoing research and identifies the needs for future research in the field. Idiopathic Pulmonary Fibrosis: A Comprehensive Clinical Guide is an important new text that provides its readers with a better understanding of the pathobiology and natural history of IPF as it continues to evolve.
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