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Blood Biomarkers in Idiopathic Pulmonary Fibrosis

Blood Biomarkers in Idiopathic Pulmonary Fibrosis

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_5437192

Blood Biomarkers in Idiopathic Pulmonary Fibrosis

About this item

Full title

Blood Biomarkers in Idiopathic Pulmonary Fibrosis

Publisher

New York: Springer US

Journal title

Lung, 2017-06, Vol.195 (3), p.273-280

Language

English

Formats

Publication information

Publisher

New York: Springer US

More information

Scope and Contents

Contents

Purpose
Idiopathic pulmonary fibrosis (IPF) is a progressive and lethal lung disease of unknown origin whose incidence has been increasing over the latest decade partly as a consequence of population ageing. New anti-fibrotic therapy including pirfenidone and nintedanib have now proven efficacy in slowing down the disease. Nevertheless, diagnosi...

Alternative Titles

Full title

Blood Biomarkers in Idiopathic Pulmonary Fibrosis

Identifiers

Primary Identifiers

Record Identifier

TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_5437192

Permalink

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_5437192

Other Identifiers

ISSN

0341-2040,1432-1750

E-ISSN

1432-1750

DOI

10.1007/s00408-017-9993-5

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