Titlebook: Idiopathic Pulmonary Fibrosis; A Comprehensive Clin Keith C. Meyer,Steven D. Nathan Book 2019Latest edition Springer Nature Switzerland AG

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Evolving Genomics of Pulmonary Fibrosis,uch technologies have been applied to lungs and cells of patients and animal models of disease with the goal of identifying key molecules with a role in pathogenesis or to develop biomarkers of disease presence, progression, and outcome as well as to identify potential drug targets. Genomics profili

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Debrief

Mimics of Idiopathic Pulmonary Fibrosis,te thoracic imaging, which in many cases may be sufficient to attain a confident diagnosis. In other cases, however, sampling of lung tissue might be necessary to confirm a usual interstitial pneumonia (UIP) histopathologic pattern if high-resolution computed tomography (HRCT) does not reveal a UIP

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Lung Transplantation for Idiopathic Pulmonary Fibrosis,to resolve fibrosis or improve lung function in IPF. Lung transplantation therefore remains the only lifesaving therapy available to treat patients with IPF. A shortage of suitable donor organs limits the number of affected individuals who can undergo this procedure, highlighting the need to allocat