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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Vydáno v:BMJ Open Respir Res
Hlavní autoři: 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
Médium: Artigo
Jazyk:Inglês
Vydáno: BMJ Publishing Group 2020
Témata:
Interstitial Lung Disease
On-line přístup: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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