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

A population-based study of coarctation of the aorta: comparisons of infants with and without associated ventricular septal defect.

Teratology - 1 Nov 2001

Wollins D S, Ferencz C, Boughman J A, Loffredo C A

Abstract excerpt

BACKGROUND: Coarctation of the aorta (CoA) is a congenital cardiovascular malformation (CCVM) sometimes associated with ventricular septal defect (VSD). Although the phenotypic association is well documented, little research exists on the epidemiological features distinguishing CoA with and witho...

Read the complete abstract on PubMed

Topics

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

Share to Age Factors
Share to Aorta
Share to Gestational Age

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Heart Defects, Congenital

Share to Heart Septal Defects, Ventricular

Share to Infant, Newborn

Share to Multivariate Analysis

Share to Pregnancy

Source

Identifiers

PMID: 11745829
DOI: 10.1002/tera.1069

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-11745829-2026-09-02.2. Manifest publication-graph-cohort-2026-09-02.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 2 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

A population-based study of coarctation of the aorta: comparisons of infants with and without associated ventricular septal defect.PMID 11745829Read ↗

Prevalence of congenital cardiovascular malformations among relatives of infants with hypoplastic left heart, coarctation of the aorta, and d‐transposition of the great arteriesSemantic proximity Read ↗

Interrupted aortic arch: An epidemiologic studySemantic proximity Read ↗

Troponin T Mutation as a Cause of Left Ventricular Systolic Dysfunction in a Young Patient with Previous Surgical Correction of Aortic Coarctation.Semantic proximity Read ↗

Bicuspid aortic valve: different clinical profiles for subjects with versus without repaired aortic coarctation.Semantic proximity Read ↗

Coarctation of the aorta: are genes relevant?Semantic proximity Read ↗

Sustained maternal hyperoxygenation improves aortic arch dimensions in fetuses with coarctationSemantic proximity Read ↗

Variants in the NOTCH1 gene in patients with aortic coarctation.Semantic proximity Read ↗

Assessment of vascular phenotype using a novel very-high-resolution ultrasound technique in adolescents after aortic coarctation repair and/or stent implantation: relationship to central haemodynamics and left ventricular mass.Semantic proximity Read ↗

[Coarctation of the aorta with aortic arch hypoplasia in newborn with partial trisomy 11q associated to 4q interstitial deletion].Semantic proximity Read ↗

Atrioventricular septal defects: Possible etiologic differences between complete and partial defectsSemantic proximity Read ↗

Cornelia de Lange syndrome in a preterm infant presenting with coarctation of aorta and perimembranous ventricular septal defect.Semantic proximity Read ↗

Prenatal diagnosis of coarctation of the aorta improves survival and reduces morbidity: Table 1Semantic proximity Read ↗

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