CT-measured pulmonary artery diameter as an independent predictor of pulmonary hypertension in cystic fibrosis

PURPOSE: The role of computed tomography (CT) scan, as a promising prognostic imaging modality in cystic fibrosis (CF), has been widely investigated, focusing on parenchymal abnormalities. The aim of the present study was to evaluate the diagnostic performance of thoracic vascular parameters on CT t...

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Detalles Bibliográficos
Publicado en:Pol J Radiol
Main Authors: Bakhshayeshkaram, Mehrdad, Aghahosseini, Farahnaz, Vaezi, Fatemeh, Kahkooei, Shahram, Salehi, Yalda, Hassanzad, Maryam, Jamaati, Hamid Reza, Velayati, Ali Akbar
Formato: Artigo
Idioma:Inglês
Publicado: Termedia Publishing House 2018
Assuntos:
Original Paper
Acceso en liña:https://ncbi.nlm.nih.gov/pmc/articles/PMC6334125/
https://ncbi.nlm.nih.gov/pubmed/30655917
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.5114/pjr.2018.79204
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