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Serial CT analysis in idiopathic pulmonary fibrosis: comparison of visual features that determine patient outcome

AIMS: Patients with idiopathic pulmonary fibrosis (IPF) receiving antifibrotic medication and patients with non-IPF fibrosing lung disease often demonstrate rates of annualised forced vital capacity (FVC) decline within the range of measurement variation (5.0%–9.9%). We examined whether change in vi...

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Detalles Bibliográficos
Autores principales:	Jacob, Joseph, Aksman, Leon, Mogulkoc, Nesrin, Procter, Alex J, Gholipour, Bahareh, Cross, Gary, Barnett, Joseph, Brereton, Christopher J, Jones, Mark G, van Moorsel, Coline H, van Es, Wouter, van Beek, Frouke, Veltkamp, Marcel, Desai, Sujal R, Judge, Eoin, Burd, Teresa, Kokosi, Maria, Savas, Recep, Bayraktaroglu, Selen, Altmann, Andre, Wells, Athol U
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	BMJ Publishing Group 2020
Materias:	Interstitial Lung Disease
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7402558/ https://www.ncbi.nlm.nih.gov/pubmed/32345689 http://dx.doi.org/10.1136/thoraxjnl-2019-213865

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