TY - BOOK ID - 14199991 TI - Idiopathic Pulmonary Fibrosis : A Comprehensive Clinical Guide AU - Meyer, Keith C. AU - Nathan, Steven D. PY - 2014 SN - 1627036814 1627036822 PB - Totowa, NJ : Humana Press : Imprint: Humana, DB - UniCat KW - Fibrosis. KW - Pulmonary fibrosis. KW - Alveolitis, Fibrosing KW - Diffuse fibrosing alveolitis KW - Diffuse interstitial pulmonary fibrosis KW - Fibrosing alveolitis KW - Hamman-Rich syndrome KW - Interstitial fibrosis of the lung KW - Interstitial pneumonia KW - Interstitial pneumonitis KW - Lungs KW - Pneumonia, Interstitial KW - Pneumonitis, Interstitial KW - Fibrosis KW - Medicine. KW - Internal medicine. KW - Respiratory organs KW - Primary care (Medicine). KW - Medicine & Public Health. KW - Pneumology/Respiratory System. KW - Internal Medicine. KW - Primary Care Medicine. KW - Diseases. KW - Primary medical care KW - Medical care KW - Respiratory diseases KW - Medicine, Internal KW - Medicine KW - Clinical sciences KW - Medical profession KW - Human biology KW - Life sciences KW - Medical sciences KW - Pathology KW - Physicians KW - Collagen diseases KW - Diseases KW - Pneumology. KW - Emergency medicine. KW - Medicine, Emergency KW - Critical care medicine KW - Disaster medicine KW - Medical emergencies KW - Respiratory organs—Diseases. KW - Primary care (Medicine) UR - https://www.unicat.be/uniCat?func=search&query=sysid:14199991 AB - 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. ER -