about
Incorporating genetics into the identification and treatment of Idiopathic Pulmonary FibrosisThe Anti-fibrotic Effects and Mechanisms of MicroRNA-486-5p in Pulmonary FibrosisNintedanib: A Review of Its Use in Patients with Idiopathic Pulmonary Fibrosis.The histone deacetylase inhibitor, romidepsin, as a potential treatment for pulmonary fibrosis.Novel Drug Targets For Idiopathic Pulmonary Fibrosis.Pirfenidone Reduces Respiratory-related Hospitalizations in Idiopathic Pulmonary Fibrosis.Pulmonary fibrosis, part I: epidemiology, pathogenesis, and diagnosis.Idiopathic Interstitial Pneumonia Associated With Autoantibodies: A Large Case Series Followed Over 1 Year.Taking the "I" out of IPF.Clarity on Endpoints for Clinical Trials in Idiopathic Pulmonary Fibrosis.
P2860
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P2860
description
2014 nî lūn-bûn
@nan
2014 թուականի Սեպտեմբերին հրատարակուած գիտական յօդուած
@hyw
2014 թվականի սեպտեմբերին հրատարակված գիտական հոդված
@hy
2014年の論文
@ja
2014年論文
@yue
2014年論文
@zh-hant
2014年論文
@zh-hk
2014年論文
@zh-mo
2014年論文
@zh-tw
2014年论文
@wuu
name
IPF clinical trial design and endpoints
@ast
IPF clinical trial design and endpoints
@en
IPF clinical trial design and endpoints
@nl
type
label
IPF clinical trial design and endpoints
@ast
IPF clinical trial design and endpoints
@en
IPF clinical trial design and endpoints
@nl
prefLabel
IPF clinical trial design and endpoints
@ast
IPF clinical trial design and endpoints
@en
IPF clinical trial design and endpoints
@nl
P2860
P1476
IPF clinical trial design and endpoints
@en
P2093
Keith C. Meyer
Steven D. Nathan
P2860
P304
P356
10.1097/MCP.0000000000000091
P407
P577
2014-09-01T00:00:00Z