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Idiopathic pulmonary fibrosis [electronic resource] : a comprehensive clinical guide / Keith C. Meyer, Steven D. Nathan, editors.

Meyer, Keith C., editor.; Nathan, Steven D., editor.
2014
RC776.F5 I35 2014
Available Online
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Title
Idiopathic pulmonary fibrosis [electronic resource] : a comprehensive clinical guide / Keith C. Meyer, Steven D. Nathan, editors.
ISBN
9781627036825 electronic book
1627036822 electronic book
9781627036818
DOI
https://doi.org/10.1007/978-1-62703-682-5
Published
New York : Humana Press, 2014.
Language
English
Description
1 online resource (xv, 451 pages) : illustrations (some color).
Item Number
10.1007/978-1-62703-682-5 doi
Call Number
RC776.F5 I35 2014
Dewey Decimal Classification
616.2/4
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.
Note
Includes index.
Access Note
Access limited to authorized users.
Source of Description
Online resource; title from PDF title page (SpringerLink, viewed October 21, 2013).
Added Author
Meyer, Keith C., editor.
Nathan, Steven D., editor.
Series
Respiratory medicine (New York, N.Y.) ; 9.
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Online Access
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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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