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Pulmonary hypertension secondary to congenital diaphragmatic hernia: factors and pathways involved i...

Pulmonary hypertension secondary to congenital diaphragmatic hernia: factors and pathways involved i...

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_proquest_miscellaneous_2184141239

Pulmonary hypertension secondary to congenital diaphragmatic hernia: factors and pathways involved in pulmonary vascular remodeling

About this item

Full title

Pulmonary hypertension secondary to congenital diaphragmatic hernia: factors and pathways involved in pulmonary vascular remodeling

Publisher

New York: Nature Publishing Group US

Journal title

Pediatric research, 2019-05, Vol.85 (6), p.754-768

Language

English

Formats

Publication information

Publisher

New York: Nature Publishing Group US

More information

Scope and Contents

Contents

Congenital diaphragmatic hernia (CDH) is a severe birth defect that is characterized by pulmonary hypoplasia and pulmonary hypertension (PHTN). PHTN secondary to CDH is a result of vascular remodeling, a structural alteration in the pulmonary vessel wall that occurs in the fetus. Factors involved in vascular remodeling have been reported in several...

Alternative Titles

Full title

Pulmonary hypertension secondary to congenital diaphragmatic hernia: factors and pathways involved in pulmonary vascular remodeling

Authors, Artists and Contributors

Identifiers

Primary Identifiers

Record Identifier

TN_cdi_proquest_miscellaneous_2184141239

Permalink

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_proquest_miscellaneous_2184141239

Other Identifiers

ISSN

0031-3998

E-ISSN

1530-0447

DOI

10.1038/s41390-019-0345-4

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