Rationale for and design of the Idiopathic Pulmonary Fibrosis–PRospective Outcomes (IPF-PRO) registry

BACKGROUND: Idiopathic pulmonary fibrosis (IPF) is a chronic interstitial lung disease characterised by progressive loss of lung function. Its clinical course is variable but ultimately fatal. There is a need for a multicentre patient registry incorporating longitudinal clinical data and biological...

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Detaylı Bibliyografya
Yayımlandı:BMJ Open Respir Res
Asıl Yazarlar: O'Brien, Emily C, Durheim, Michael T, Gamerman, Victoria, Garfinkel, Sandy, Anstrom, Kevin J, Palmer, Scott M, Conoscenti, Craig S
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: BMJ Publishing Group 2016
Konular:
Interstitial Lung Disease
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC4716211/
https://ncbi.nlm.nih.gov/pubmed/26835134
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1136/bmjresp-2015-000108
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