Results 151 to 160 of about 69,400 (250)

Congenital heart disease in pregnancy and severe maternal morbidity: A distributed data network study

Pregnancy, Volume 2, Issue 5, September 2026.
Abstract Introduction Pregnant people with congenital heart disease (CHD) are a growing patient population in obstetrics, yet evidence on the risk for severe maternal morbidity (SMM) has largely been limited to studies that lack specificity for CHD. We conducted this study to demonstrate the utility of distributed data networks for obstetric research ...
Elizabeth B. Sherwin, Benjamin Martin, Xiao Xu, Anna Booman, Alyssa Howren, Kimberlee McKay, Sadaf Kazi, Sean O'Reilly, Katie S. Kolla, Khyzer Aziz, Katherine Bianco, Stephanie A. Leonard   +11 more
wiley   +1 more source

Transcatheter Tricuspid Valve Embolization: Revealing Critical Limitations of Contemporary Valve Design. [PDF]

JACC Case Rep
Aalaei-Andabili SH, Anderson D, Kwiatkowski SG, Chahal DS.   +3 more
europepmc   +1 more source

Society for Maternal‐Fetal Medicine Special Statement: Quality metrics to assess prenatal detection of congenital heart defects—Updated 2026

Pregnancy, Volume 2, Issue 5, September 2026.
Abstract Congenital heart defects (CHDs) are a leading cause of neonatal morbidity and mortality. Accurate prenatal diagnosis of CHDs can reduce morbidity and mortality by improving prenatal care, facilitating predelivery pediatric cardiology consultation, and directing delivery to facilities with resources to manage the complex medical and surgical ...
Society for Maternal‐Fetal Medicine (SMFM), Adina Kern‐Goldberger, C. Andrew Combs, Afshan B. Hameed, Iffath Abbasi Hoskins, SMFM Patient Safety and Quality Committee   +5 more
wiley   +1 more source

Tricuspid Valve Regurgitation Manifesting in Gastrointestinal Symptoms. [PDF]

JACC Case Rep
Pérez-Soto N, Fregoso-Sánchez A, Miguel-González JJ, Everding-Rodríguez AG, Pacheco-Bouthiller AD, Ferreira-Piña B, González-Martínez A, Lomelí-Sánche ÓS.   +7 more
europepmc   +1 more source

Placental pathology in fetuses with and without congenital heart defects

Pregnancy, Volume 2, Issue 5, September 2026.
Abstract Introduction Placental histopathologic evaluation of pregnancies affected by congenital heart defects (CHDs) can provide insight into the mechanism connecting placental and fetal vascular systems. The objective of this study was to evaluate the prevalence of maternal vascular malperfusion (MVM) and fetal vascular malperfusion (FVM) lesions of ...
Tucker E. Doiron, Sherri Besmer, Jessenia Guerrero, Joanne Salas, Lauren Fox, Emily Zantow, Niraj R. Chavan   +6 more
wiley   +1 more source

Persistent Hypoxia After Tricuspid Valve Replacement. [PDF]

JACC Case Rep
Nguyen J, Merino T, Kandula V, Castillo Kontak L, Mercado Garcia R, Caldera A, Shankar A, Gonzalez R, Neravetla S, Condado JF.   +9 more
europepmc   +1 more source

The Tricuspid Valve

Journal of the American College of Cardiology, 2021
openaire   +1 more source

Multiple Modelling Methods Suggest That Grain‐Free Diets Are Not Predictive of New Owner‐Reported Cardiac Diagnoses Over Two Years in the Dog Aging Project, Despite Owner Misclassification of Diet

Veterinary Medicine and Science, Volume 12, Issue 5, September 2026.
ABSTRACT Background Grain‐free diets have been potentially linked to dilated cardiomyopathy (DCM) in several studies in dogs, although the underlying mechanisms for this potential link, if present, are unclear. Additionally, some studies have found no association between grain‐free diets and DCM in dogs.
Janice O'Brien, Morgan Bishop, Dog Aging Project Consortium, M. Katherine Tolbert, Audrey Ruple   +4 more
wiley   +1 more source

Valve-in-Valve Implantation for Early Failure of a Transcatheter Tricuspid Valve. [PDF]

JACC Case Rep
Boukantar M, Aouate D, Chiaroni PM, Zamora P, Truong T, Molho A, Labidi O, Boyer C, Teiger E, Gallet R.   +9 more
europepmc   +1 more source

Novel Postzygotic Variants Associated With Hypomelanosis of Ito Expand the ACTB‐Related Neurocutaneous Disease Spectrum

Clinical Genetics, Volume 110, Issue 3, Page 369-373, September 2026.
We describe a previously unreported phenotype related to postzygotic ACTB variants with hypomelanosis of Ito, characterized by hypopigmentation associated or not with neurodevelopmental features, distinct from Becker presentations, bridging constitutional neurodevelopmental and somatic cutaneous phenotypes.
Estella Castillon, Paul Rollier, Didier Bessis, Laurent Pasquier, Caroline Racine, Alexis Praga, Pierre Vabres, Bertille Bonniaud, Paul Kuentz, Laurence Faivre   +9 more
wiley   +1 more source