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

高度

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

抵消

anthesis

感染

propose

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

即席

Paraplegia

locus-ceruleus

營養(yǎng)

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