Comparison of the quantitative CT imaging biomarkers of idiopathic pulmonary fibrosis at baseline and early change with an interval of 7 months.

Rationale and Objectives: Median survival of patients with idiopathic pulmonary fibrosis (IPF) is 2-5 years. Sensitive imaging metrics can play a role in detecting early changes in therapeutic development. The aim of the present study was to compare known computed tomography (CT) histogram kurtosis...

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Detalles Bibliográficos
Publicado en:Academic Radiology Vol. 22; no. 1; pp. 70 - 81
Autores principales: Kim, Hyun J, Brown, Matthew S, Chong, Daniel, Gjertson, David W, Lu, Peiyun, Kim, Hak J, Coy, Heidi, Goldin, Jonathan G
Formato: research Journal Article
Publicado: Elsevier B.V. Jan2015
Acceso en línea:Ver este registro en EBSCOhost