Results 181 to 190 of about 50,118 (258)

Exploring hemodynamic alterations in gastroschisis: insights into fetal growth restriction using prenatal MRI

Ultrasound in Obstetrics &Gynecology, Volume 67, Issue 6, Page 795-805, June 2026.
Abstract Objective Despite the high incidence of fetal growth restriction (FGR) in gastroschisis (GS) associated with placental fetal vascular malperfusion (FVM), the underlying mechanism remains unclear. We aimed to investigate whether umbilical vein (UV) stenosis at the abdominal wall defect impairs fetoplacental circulation, leading to FGR.
H. Shi, D. Prayer, P. Kienast, R. Stepponat, C. Mitter, J. Tischer, X. Li, J. Binder, G. Kasprian   +8 more
wiley   +1 more source

A Delayed Approach to Ventricular Septal Defect Repair After Myocardial Infarction. [PDF]

JACC Case Rep
Al Kindi S, Al-Jabri A, Maddali MM, Al Abri Q.   +3 more
europepmc   +1 more source

Cardiovascular Health in Women—Across the Lifespan

Clinical Endocrinology, Volume 104, Issue 6, Page 539-555, June 2026.
ABSTRACT Cardiovascular disease (CVD) remains the leading cause of mortality and morbidity among women worldwide. However, CVD continues to be perceived as a predominantly male issue. CVD in women therefore remains understudied, underrecognized and undertreated.
Jaya Chandrasekhar, Jessica Yao, Simone Gong, Madhuka Wijayarathne, Monique Watts, Swati Mukherjee   +5 more
wiley   +1 more source

Pregnancy with Doubly Committed Subarterial Ventricular Septal Defect: Management Challenges and Delayed Maternal Risk Stratification. [PDF]

Int Med Case Rep J
Roseli A, Setiawan D, Cool CJ.
europepmc   +1 more source

Expanding the Phenotypic Spectrum Associated With Loss‐of‐Function SMARCA4 Variants to Eye Developmental Anomalies

Clinical Genetics, Volume 109, Issue 6, Page 1064-1069, June 2026.
This study expands the clinical spectrum of SMARCA4 by describing a novel phenotype in three unrelated individuals with truncating variants. Distinct from Coffin–Siris syndrome and rhabdoid tumor predisposition, this new association is characterized by ocular malformations, specifically microphthalmia and coloboma.
Bertrand Chesneau, Marjolaine Willems, Abdelhakim Bouazzaoui, Léopoldine Lequeux, Julie Plaisancié, Salima El Chehadeh, Hélène Dollfus, Nicolas Chassaing   +7 more
wiley   +1 more source

Expanding Phenotype of GINS1 Deficiency: A Case Report and Review of the Literature

Clinical Genetics, Volume 109, Issue 6, Page 1076-1080, June 2026.
The authors present a novel case and review of individuals with GINS1 deficiency, causing severe growth restriction and combined immunodeficiency. Only the ninth case of this ultrarare disorder, it highlights the role of these variants in disease, glaucoma as a feature, and the possibility of immunodeficiency without infections in affected individuals.
Michael P. Mackley, Rae Brager, Hannah Geddie, Vicky Breakey, Rebecca Hough, Dimitrios J. Stavropoulos, Vanda McNiven   +6 more
wiley   +1 more source

Kinetics of spontaneous residual shunt closure: a comparative analysis between two surgical procedures for perimembranous ventricular septal defect. [PDF]

J Thorac Dis
Xiang M, Pan Z, Xi L.
europepmc   +1 more source

Aortic Root Replacement in Patients With Ventricular Septal Defect. [PDF]

Ann Thorac Surg Short Rep
Takahashi R, Munakata H, Okada K, Hayashi T, Seto T, Suda H, Okita Y.   +6 more
europepmc   +1 more source

Survival of a Large Traumatic Ventricular Septal Defect Caused by a Firework Explosion. [PDF]

Eur J Cardiothorac Surg
Freystaetter K, Finster A, Karner M, Valicek G, Wiedemann D, Bergmann P.   +5 more
europepmc   +1 more source