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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Bibliografski detalji
Izdano u:Pol J Radiol
Glavni autori: Bakhshayeshkaram, Mehrdad, Aghahosseini, Farahnaz, Vaezi, Fatemeh, Kahkooei, Shahram, Salehi, Yalda, Hassanzad, Maryam, Jamaati, Hamid Reza, Velayati, Ali Akbar
Format: Artigo
Jezik:Inglês
Izdano: Termedia Publishing House 2018
Teme:
Original Paper
Online pristup: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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