Idiopathic Pulmonary Fibrosis: A Comprehensive Clinical Guide ...
WEBThis book is a comprehensive guide to our current understanding of idiopathic pulmonary fibrosis (IPF), its disease pathogenesis, genetic underpinnings, diagnosis, and management. New topics include: classification of interstitial lung disease, pulmonary function tests in IPF, and biomarkers.
Idiopathic Pulmonary Fibrosis: A Comprehensive Clinical Guide ...
WEBJan 4, 2019 · This book is a comprehensive guide to our current understanding of idiopathic pulmonary fibrosis (IPF), its disease pathogenesis, genetic underpinnings, diagnosis, and management.
- Reviews: 5
Idiopathic Pulmonary Fibrosis 1st Edition - amazon.com
WEBAug 27, 2018 · Covers the process of making the diagnosis of idiopathic pulmonary fibrosis, as well as IPF look-alikes: uncharacterized PF, CTD-ILD, and cHP. Details today’s available therapeutics, including Rx, rehabilitation, O2, Tx, …
- Reviews: 1
- Author: Jeffrey Swigris, Kevin K Brown MD
Idiopathic pulmonary fibrosis in adults: diagnosis and management
WEBMay 1, 2017 · Idiopathic pulmonary fibrosis is a chronic, progressive fibrotic interstitial lung disease of unknown origin. It is a difficult disease to diagnose and often requires the collaborative expertise of a consultant respiratory physician, radiologist and histopathologist to reach a consensus diagnosis.
Idiopathic Pulmonary Fibrosis: A Comprehensive Clinical Guide ...
WEBAug 23, 2016 · 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.
Idiopathic Pulmonary Fibrosis - Google Books
WEBDec 14, 2018 · This book is a comprehensive guide to our current understanding of idiopathic pulmonary fibrosis (IPF), its disease pathogenesis, genetic underpinnings, diagnosis, and management.
Idiopathic Pulmonary Fibrosis - ScienceDirect
WEBIdiopathic pulmonary fibrosis (IPF) is a complex disease that is limited to the lungs. The natural history of IPF is one of slow and progressive decline in lung function with most patients dying from respiratory failure within 2–5 years of diagnosis.
Idiopathic Pulmonary Fibrosis: Advances in Diagnostic Tools
WEBFrom epidemiology and pathogenesis to disease management, this book reviews our current understanding of and provides up-to-date information of Idiopathic Pulmonary Fibrosis (IPF).
Idiopathic Pulmonary Fibrosis - Google Books
WEBOct 16, 2013 · Idiopathic Pulmonary Fibrosis: A Comprehensive Clinical Guide delivers a concise review of our current understanding of disease pathogenesis and provides current evidence in the...
Idiopathic Pulmonary Fibrosis - European Respiratory Society
WEBIdiopathic pulmonary fibrosis (IPF) is a steadily progressive and ultimately fatal disease of unknown origin. Recent years have seen advances in our understanding of IPF and a number of guidelines have been published. But many questions remain unanswered, particularly surrounding probable versus definite IPF.