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Alteration of cystic airway mesenchyme in congenital pulmonary airway malformation

Alteration of cystic airway mesenchyme in congenital pulmonary airway malformation

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_6439218

Alteration of cystic airway mesenchyme in congenital pulmonary airway malformation

About this item

Full title

Alteration of cystic airway mesenchyme in congenital pulmonary airway malformation

Publisher

London: Nature Publishing Group UK

Journal title

Scientific reports, 2019-03, Vol.9 (1), p.5296, Article 5296

Language

English

Formats

Publication information

Publisher

London: Nature Publishing Group UK

More information

Scope and Contents

Contents

Congenital pulmonary airway malformation (CPAM) is the most common congenital lesion detected in the neonatal lung, which may lead to respiratory distress, infection, and pneumothorax. CPAM is thought to result from abnormal branching morphogenesis during fetal lung development, arising from different locations within the developing respiratory tra...

Alternative Titles

Full title

Alteration of cystic airway mesenchyme in congenital pulmonary airway malformation

Identifiers

Primary Identifiers

Record Identifier

TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_6439218

Permalink

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_6439218

Other Identifiers

ISSN

2045-2322

E-ISSN

2045-2322

DOI

10.1038/s41598-019-41777-y

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