A PATCH FOR VENTRICULAR SEPTAL DEFECTS DESIGNED TO AVOID HEART BLOCK [PDF]
openaire +2 more sources
Diagnostic value of synchronized phonocardiogram-electrocardiogram monitoring in children with ventricular septal defect. [PDF]
Zhang Y +7 more
europepmc +1 more source
American Journal of Medical Genetics Part A, Volume 200, Issue 6, Page 1427-1430, June 2026.
Alberto De Rosa +7 more
wiley +1 more source
Early Outcomes of Real‐World Aortic Valve Replacement With RESILIA Tissue in the Chinese Population
In this real‐world study of 250 Chinese patients scheduled for elective aortic valve replacement, the INSPIRIS RESILIA aortic valve demonstrated favorable 1‐year safety, with a 98.0% rate of freedom from all‐cause mortality and no observed structural valve deterioration, alongside stable hemodynamic performance.
Haitao Xu +4 more
wiley +1 more source
Totally Endoscopic Patch Repair for Ruptured Sinus of Valsalva Aneurysm Associated With Ventricular Septal Defect. [PDF]
Maeda S, Kato R, Ito T.
europepmc +1 more source
This work presents a novel computational simulation framework for the study of pulmonary venous hemodynamics that integrates a closed‐loop lumped parameter model (LPM) of the cardiovascular system with a computational fluid dynamics (CFD) model of the pulmonary veins and left atrium. Coupling of the LPM and CFD models was accomplished through surrogate
Alessia Di Nardo +3 more
wiley +1 more source
Congenital Pericardial Agenesis: An Innocent Finding or Clinically Significant Condition? A Case Series and Literature Review. [PDF]
Groudeva V +3 more
europepmc +1 more source
Percutaneous closure of ventricular septal rupture after myocardial infarction: a case report of competing timelines in multifactorial shock. [PDF]
Cook TA +4 more
europepmc +1 more source
Prosthesis-Free Repair of Partial Atrioventricular Septal Defect in Down Syndrome: A Valve-Sparing Technique. [PDF]
Jonjev ŽS +4 more
europepmc +1 more source
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

