Results 131 to 140 of about 63,827 (265)
Journal of Arrhythmia, Volume 42, Issue 3, June 2026.We report a case of MEPPC syndrome presenting with severe dilated cardiomyopathy due to a pathogenic SCN5A p.Arg814Trp variant. Genetic diagnosis enabled precision pharmacotherapy with hydroquinidine, which suppressed multifocal Purkinje‐origin ectopy resistant to catheter ablation and led to marked improvement in left ventricular function.
Jonathan L. Ciofani +2 more
wiley +1 more source
Journal of Arrhythmia, Volume 42, Issue 3, June 2026.In the prospective multicenter study, left bundle branch area pacing using stylet‐driven pacing leads demonstrated a high procedural success rate and showed stable lead performance during long‐term follow‐up. ABSTRACT Background Right ventricular pacing increases the risk of dyssynchrony, which raises the need for more physiological pacing strategies ...
Ga‐In Yu +12 more
wiley +1 more source
Primitive hepatic venous plexus in a child with scimitar syndrome and pulmonary sequestration [PDF]
, 2013 This article reports a case of scimitar syndrome with pulmonary sequestration, persistent primitive hepatic venous plexus and stenosis of the inferior vena cava in a child presenting with failure to thrive.
Morrison, M.L. +2 more
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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 +5 more
wiley +1 more source
, 2015 Atrial septal defect (ASD) is a hole in the atrial septum that allows blood flow to shunt between the left and right atria. These defects are generally characterized as secundum type (hole in the septum primum) and sinus venosus type (hole in the atrial septum that is associated with the superior vena cava/inferior vena cava and accompanying anomalous ...
openaire +2 more sources
Advanced Science, Volume 13, Issue 26, 8 May 2026.Lipid overload suppresses SREBF2‐mediated FNTB expression, leading to defective Lamin A maturation and nuclear envelope instability. This nuclear catastrophe triggers a pro‐fibrotic senescence program in cardiomyocytes. Notably, restoring nuclear integrity via AAV9‐based gene therapy effectively attenuates cardiac remodeling, identifying the ...
Yuxiao Chen +16 more
wiley +1 more source
The morphologic variability in atrioventricular valvar atresia [PDF]
, 2008 Anderson, RH, Ho, SY, Rigby, ML
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Genetic and Phenotypic Features of the Five Known Polyaminopathies: A Critical Narrative Review
American Journal of Medical Genetics Part A, Volume 200, Issue 5, Page 993-1003, May 2026.ABSTRACT Polyaminopathies are a recently described family of rare genetic neurodevelopmental disorders. Polyaminopathies disrupt the biosynthesis of the primary polyamines: putrescine, spermidine, and spermine. Snyder–Robinson syndrome results from hemizygous loss‐of‐function variants in the spermine synthase (SMS) gene, resulting in decreased or ...
Elizabeth A. VanSickle +26 more
wiley +1 more source
P5486Vestibular atrial septal defects: a novel atrial septal defect [PDF]
European Heart Journal, 2018 R Loomba, D E Spicer, R H Anderson
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