Time to diagnosis of idiopathic pulmonary fibrosis in the IPF-PRO Registry

BACKGROUND: Idiopathic pulmonary fibrosis (IPF) is a progressive disease with high mortality. Patient characteristics associated with diagnostic delays are not well described. METHODS: Subjects who had not been diagnosed with IPF prior to referral and received a new diagnosis of IPF at an enrolling...

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Bibliografski detalji
Izdano u:BMJ Open Respir Res
Glavni autori: Snyder, Laurie D, Mosher, Christopher, Holtze, Colin H, Lancaster, Lisa H, Flaherty, Kevin R, Noth, Imre, Neely, Megan L, Hellkamp, Anne S, Bender, Shaun, Conoscenti, Craig S, de Andrade, Joao A, Whelan, Timothy PM
Format: Artigo
Jezik:Inglês
Izdano: BMJ Publishing Group 2020
Teme:
Interstitial Lung Disease
Online pristup:https://ncbi.nlm.nih.gov/pmc/articles/PMC7337884/
https://ncbi.nlm.nih.gov/pubmed/32624493
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1136/bmjresp-2020-000567
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