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• W2000565423 abstract "Idiopathic pulmonary fibrosis (IPF) is a chronic, progressive, and ultimately fatal disease of the lung with an unknown etiology and few treatment options. Recognition of patients who fall into phenotypic subsets may provide earlier opportunities for initiation of therapy or referral to transplant. In addition, identification and management of comorbidities may improve quality of life, and this may be more important to some patients than extending survival. This chapter updates prior summaries of proposed phenotypes and comorbidities in IPF (Fell, 2012)." @default.
• W2000565423 created "2016-06-24" @default.
• W2000565423 creator A5070747341 @default.
• W2000565423 creator A5074594962 @default.
• W2000565423 date "2018-01-01" @default.
• W2000565423 modified "2023-10-17" @default.
• W2000565423 title "Idiopathic Pulmonary Fibrosis" @default.
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• W2000565423 doi "https://doi.org/10.1016/b978-0-323-48024-6.00010-0" @default.
• W2000565423 hasPublicationYear "2018" @default.
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