Idiopathic Pulmonary Fibrosis
eBook - PDF

Idiopathic Pulmonary Fibrosis

  1. 800 pages
  2. English
  3. PDF
  4. Available on iOS & Android
eBook - PDF

Idiopathic Pulmonary Fibrosis

About this book

A discussion of the epidemiology, clinical features, and differential diagnoses of idiopathic pulmonary fibrosis (IPF). Key topics include the role of polymorphonuclear leukocytes in the pathogenesis of pulmonary fibrosis, and current treatment options, including medical therapy and lung transplantation.

Frequently asked questions

Yes, you can cancel anytime from the Subscription tab in your account settings on the Perlego website. Your subscription will stay active until the end of your current billing period. Learn how to cancel your subscription.
At the moment all of our mobile-responsive ePub books are available to download via the app. Most of our PDFs are also available to download and we're working on making the final remaining ones downloadable now. Learn more here.
Perlego offers two plans: Essential and Complete
  • Essential is ideal for learners and professionals who enjoy exploring a wide range of subjects. Access the Essential Library with 800,000+ trusted titles and best-sellers across business, personal growth, and the humanities. Includes unlimited reading time and Standard Read Aloud voice.
  • Complete: Perfect for advanced learners and researchers needing full, unrestricted access. Unlock 1.4M+ books across hundreds of subjects, including academic and specialized titles. The Complete Plan also includes advanced features like Premium Read Aloud and Research Assistant.
Both plans are available with monthly, semester, or annual billing cycles.
We are an online textbook subscription service, where you can get access to an entire online library for less than the price of a single book per month. With over 1 million books across 1000+ topics, we’ve got you covered! Learn more here.
Look out for the read-aloud symbol on your next book to see if you can listen to it. The read-aloud tool reads text aloud for you, highlighting the text as it is being read. You can pause it, speed it up and slow it down. Learn more here.
Yes! You can use the Perlego app on both iOS or Android devices to read anytime, anywhere — even offline. Perfect for commutes or when you’re on the go.
Please note we cannot support devices running on iOS 13 and Android 7 or earlier. Learn more about using the app.
Yes, you can access Idiopathic Pulmonary Fibrosis by Joseph P. Lynch in PDF and/or ePUB format, as well as other popular books in Medicine & Pulmonary & Thoracic Medicine. We have over one million books available in our catalogue for you to explore.

Information

Publisher
CRC Press
Year
2003
eBook ISBN
9780203913444

Table of contents

  1. Front Cover
  2. INTRODUCTION
  3. PREFACE
  4. CONTRIBUTORS
  5. CONTENTS
  6. Chapter 1. Epidemiology of Idiopathic Pulmonary Fibrosis
  7. Chapter 2. Genetics of Familial Pulmonary Fibrosis and Other Variants
  8. Chapter 3. Clinical Features and Differential Diagnosis of Idiopathic Pulmonary Fibrosis
  9. Chapter 4. Pathology of Usual Interstitial Pneumonia
  10. Chapter 5. Nonspecific Interstitial Pneumonia
  11. Chapter 6. Role of Physiological Assessment in Usual Interstitial Pneumonia
  12. Chapter 7. Role of High-Resolution Thin Section Computed Tomographic Scanning
  13. Chapter 8. Other Imaging Techniques for Idiopathic Interstitial Pneumonias
  14. Chapter 9. Bronchoalveolar Lavage in Interstitial Lung Disease
  15. Chapter 10. Pulmonary Fibrosis in Connective Tissue Disease
  16. Chapter 11. Cytokine Phenotypes and the Progression of Chronic Pulmonary Fibrosis
  17. Chapter 12. CXC Chemokines in Angiogenesis Related to Pulmonary Fibrosis
  18. Chapter 13. Role of Polymorphonuclear Leukocytes in the Pathogenesis of Idiopathic Pulmonary Fibrosis
  19. Chapter 14. Integrins and Pulmonary Fibrosis
  20. Chapter 15. Oxidants and Antioxidants in Idiopathic Pulmonary Fibrosis
  21. Chapter 16. Fibrin Turnover in Pulmonary Fibrosis
  22. Chapter 17. Arachidonic Acid Metabolites: Potential Mediators and Therapeutic Targets in Fibrotic Lung Disease
  23. Chapter 18. Matrix Metalloproteinases and Tissue Inhibitors of Metalloproteinases in Pulmonary Fibrosis
  24. Chapter 19. Extracellular Matrix
  25. Chapter 20. Role of Fibroblasts and Myofibroblasts in Idiopathic Pulmonary Fibrosis
  26. Chapter 21. Peptide and Provisional Matrix Signals in Idiopathic Pulmonary Fibrosis
  27. Chapter 22. Role of Alveolar Type II Epithelial Cells in Pulmonary Fibrosis
  28. Chapter 23. Surfactant Proteins in the Pathophysiology of Pulmonary Fibrosis
  29. Chapter 24. Bronchiolar Epithelium in Idiopathic Pulmonary Fibrosis/Usual Interstitial Fibrosis
  30. Chapter 25. Role of Viruses in the Pathogenesis of Pulmonary Fibrosis
  31. Chapter 26. Current Treatment Options
  32. Chapter 27. Future Directions in the Treatment of Idiopathic Pulmonary Fibrosis
  33. Chapter 28. Future Directions in Genetic Strategies for Understanding and Treating Idiopathic Pulmonary Fibrosis
  34. INDEX
  35. Back Cover