Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

ABCA3 mutation and pulmonary hypertension: a link with alveolar capillary dysplasia?

The Journal of pediatrics - 1 Jun 2008

Danhaive Olivier, Peca Donatella, Boldrini Renata

Abstract excerpt

No abstract is available from the source.

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to ATP-Binding Cassette Transporters
Share to Capillaries
Share to Fatal Outcome
Share to ABCA3 gene

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Hypertension, Pulmonary

Share to Infant

Share to Mutation

Share to Pulmonary Alveoli

Source

Identifiers

PMID: 18492541
DOI: 10.1016/j.jpeds.2008.01.019

Genes

ABCA3

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

ABCA3 mutation and pulmonary hypertension: a link with alveolar capillary dysplasia?PMID 18492541Read ↗

A child with severe pneumomediastinum and ABCA3 gene mutation: a puzzling connection.Semantic proximity Read ↗

Combined pulmonary fibrosis and emphysema syndrome associated with ABCA3 mutations.Semantic proximity Read ↗

ABCA3 mutations led to pulmonary fibrosis and emphysema with pulmonary hypertension in an 8-year-old girl.Semantic proximity Read ↗

Phenotypic and genetic spectrum of alveolar capillary dysplasia: a retrospective cohort study.Semantic proximity Read ↗

A homozygous variant in ABCA3 is associated with severe respiratory distress and early neonatal death.Semantic proximity Read ↗

ABCA3 deficiency: neonatal respiratory failure and interstitial lung disease.Semantic proximity Read ↗

ABCA3 mutations in adult pulmonary fibrosis patients: a case series and review of literature.Semantic proximity Read ↗

[A novel compound heterozygous mutation in ABCA3 gene in a child with diffuse parenchymal lung disease].Semantic proximity Read ↗

ABCA3, a key player in neonatal respiratory transition and genetic disorders of the surfactant system.Semantic proximity Read ↗

Bi-allelic missenseABCA3mutations in a patient with childhood ILD who reached adulthoodSemantic proximity Read ↗

A large kindred of pulmonary fibrosis associated with a novel ABCA3 gene variant.Semantic proximity Read ↗

Ultrastructural and molecular analysis in fatal neonatal interstitial pneumonia caused by a novel ABCA3 mutationSemantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.