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Idiopathic pulmonary fibrosis: pathogenesis and management

Idiopathic pulmonary fibrosis: pathogenesis and management

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_doaj_primary_oai_doaj_org_article_ca7311210c99444785dbc12e2154d9e1

Idiopathic pulmonary fibrosis: pathogenesis and management

About this item

Full title

Idiopathic pulmonary fibrosis: pathogenesis and management

Publisher

England: BioMed Central Ltd

Journal title

Respiratory research, 2018-02, Vol.19 (1), p.32-32, Article 32

Language

English

Formats

Publication information

Publisher

England: BioMed Central Ltd

More information

Scope and Contents

Contents

Idiopathic pulmonary fibrosis (IPF) is a chronic, progressive disease characterized by the aberrant accumulation of fibrotic tissue in the lungs parenchyma, associated with significant morbidity and poor prognosis. This review will present the substantial advances achieved in the understanding of IPF pathogenesis and in the therapeutic options that...

Alternative Titles

Full title

Idiopathic pulmonary fibrosis: pathogenesis and management

Identifiers

Primary Identifiers

Record Identifier

TN_cdi_doaj_primary_oai_doaj_org_article_ca7311210c99444785dbc12e2154d9e1

Permalink

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_doaj_primary_oai_doaj_org_article_ca7311210c99444785dbc12e2154d9e1

Other Identifiers

ISSN

1465-993X,1465-9921

E-ISSN

1465-993X

DOI

10.1186/s12931-018-0730-2

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