Results 51 to 60 of about 5,762 (257)

Maternal Myo‐Inositol Intake and Congenital Heart Defects in Offspring: A Population‐Based Case–Control Study

open access: yesBJOG: An International Journal of Obstetrics &Gynaecology, Volume 133, Issue 3, Page 442-453, February 2026.
ABSTRACT Objective To investigate associations between maternal periconceptional (three months prior through the third pregnancy month) myo‐inositol intake and the odds of selected congenital heart defects in offspring. Design A population‐based case–control study using the National Birth Defects Prevention Study (NBDPS) database. Setting United States.
Ruiqi Cen   +16 more
wiley   +1 more source

Pure Duplication of the Distal Long Arm of Chromosome 15 with Ebstein Anomaly and Clavicular Anomaly

open access: yesCase Reports in Genetics, 2011
This report is of a patient with pure trisomy of 15q24-qter who presents with the rare Ebstein anomaly and a previously unreported skeletal anomaly. Chromosome microarray analysis allowed high-resolution identification of the extent of the trisomy and ...
Rachel O'Connor   +7 more
doaj   +1 more source

Diagnóstico ecográfico de la malformación de la válvula tricúspide en un perro [PDF]

open access: yes, 1998
Se describe un caso de diplasia de la válvula tricúspide en un perro macho mestizo de nueve meses de ...
Carretero i Romay, Ana   +4 more
core  

Centered Partition Process: Informative Priors for Clustering

open access: yes, 2019
There is a very rich literature proposing Bayesian approaches for clustering starting with a prior probability distribution on partitions. Most approaches assume exchangeability, leading to simple representations in terms of Exchangeable Partition ...
Dunson, David B.   +3 more
core   +1 more source

Grit in the Workplace Experienced by Taiwanese Adults With Congenital Heart Disease: A Phenomenological Study

open access: yesJournal of Clinical Nursing, Volume 35, Issue 2, Page 866-878, February 2026.
ABSTRACT Aim To explore how adults with congenital heart disease (ACHD) experience and express grit in the workplace. Design Qualitative study using Husserl's descriptive phenomenology. Methods Between March 2022 and June 2023, semi‐structured interviews were administered to 18 ACHD recruited from two medical centre outpatient departments.
Yu‐Shiu Liu   +5 more
wiley   +1 more source

Copy number variants in Ebstein anomaly. [PDF]

open access: yesPLoS ONE, 2017
Ebstein anomaly (EA) is a rare congenital defect characterized by apical displacement of the septal tricuspid leaflets and atrialization of the right ventricle. The etiology of EA is unclear; however, recurrence in families and the association of EA with
Andreas Giannakou   +10 more
doaj   +1 more source

Cardiac MRI predictors of right ventricular dysfunction after the Da Silva cone operation for Ebstein's anomaly

open access: yesInternational Journal of Cardiology Congenital Heart Disease, 2022
Introduction: Despite the clinical benefits of the cone operation for Ebstein's anomaly, significant right ventricular (RV) dysfunction is frequently seen immediately after the procedure and if persistent may portend worse long-term outcomes.
Tarek Alsaied   +14 more
doaj   +1 more source

Management and outcome of Ebstein's anomaly in children [PDF]

open access: yes, 2017
Objectives To assess clinical presentation, treatment, and outcome of children with Ebstein's anomaly. Background Data on long-term outcome of children with Ebstein's anomaly are scarce.
Attenhofer Jost, Christine H.   +8 more
core  

Combining Detailed Fetal Anatomy Scanning in the NT Window Versus Early Second Trimester Scanning at 14–16 Weeks

open access: yesJournal of Ultrasound in Medicine, Volume 45, Issue 1, Page 105-113, January 2026.
Objectives First‐trimester ultrasound has evolved to incorporate a detailed fetal anatomy scan (FAS) with nuchal translucency (NT) screening. Many institutions use a 2‐visit protocol: NT followed by detailed FAS at 14–16 weeks. We aimed to evaluate whether integrating detailed FAS into the NT window (12 + 5 to 13 + 6 weeks) is non‐inferior in ...
Tomer Shwartz   +6 more
wiley   +1 more source

Analysis of enriched rare variants in JPH2-encoded junctophilin-2 among Greater Middle Eastern individuals reveals a novel homozygous variant associated with neonatal dilated cardiomyopathy. [PDF]

open access: yes, 2019
Junctophilin-2 (JPH2) is a part of the junctional membrane complex that facilitates calcium-handling in the cardiomyocyte. Previously, missense variants in JPH2 have been linked to hypertrophic cardiomyopathy; however, pathogenic "loss of function" (LOF)
Allen, HD   +11 more
core   +1 more source

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