The Presence of Patent Foramen Ovale in the Superior Type of Sinus Venosus Atrial Septal Defect
, 2020 Niloufar Samiei +4 more
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Assessment of left atrial remodeling using speckle tracking echocardiography after percutaneous atrial septal defect closure in adult patients [PDF]
, 2022 Ji‐Hoon Choi +13 more
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Genetic Diagnoses Among Congenital Anomaly Cases in Europe: Data From the EUROCAT Network
Paediatric and Perinatal Epidemiology, EarlyView.ABSTRACT Background Surveillance of congenital anomaly prevalence over time can identify new teratogens. Anomalies with a genetic cause are excluded from the monitoring. Objectives We examined temporal changes in the proportion of genetic diagnoses among cases with a congenital anomaly.
Jorieke E. H. Bergman +23 more
wiley +1 more source
, 2010 The population of adults with congenital heart disease (CHD) is rapidly growing as a result of improvement in diagnostic techniques, medical and surgical expertise. It is estimated that 85% of infants born with CHD survive into adulthood, some of whom have never had any intervention or surgery.
openaire +2 more sources
Characterization of Atrial Septal Defect Occluders by right and left atrial pull-out forces [PDF]
, 2019 Markus Brudsche, B. Ismer, Nikolaus Haas
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Experimental Physiology, EarlyView.Summary of the timeline of characterized events related to atrial fibrilation (AF) and diastolic dysfunction in a mouse heart failure with preserved ejection fraction (HFpEF) model. Three weeks after the initiation of the diet regimen with high fat diet (HFD) and Nω‐nitro‐l‐arginine methyl ester (l‐NAME) in drinking water to induce HFpEF, significantly
Bernadin Ndongson‐Dongmo +2 more
wiley +1 more source
Pericardial patch for atrial septal defect closure [PDF]
, 1999 Sanjeeth Peter
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Inappropriate shocks from a transvenous implantable defibrillator caused by atrial fibrillation and a missed atrial septal defect in a patient with a modified Bentall procedure [PDF]
, 2021 Άννα Κωστοπούλου +3 more
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Evaluating the Genetic Overlap Between Congenital Heart Disease and Neuroblastoma Risk
Pediatric Blood &Cancer, Volume 73, Issue 2, February 2026.ABSTRACT Children with congenital heart disease (CHD) have elevated neuroblastoma (NB) risk, potentially due to shared neural crest origins. We analyzed rare exonic de novo single‐nucleotide variants in 702 CHD and 454 NB trios from the Neuroblastoma Epidemiology in North America Study, Gabriella Miller Kids First Program, and a published cohort. Seven
Ji Yun Tark +7 more
wiley +1 more source
Difficult pacemaker implantation. Detection of a wrong course due to sinus venosus type atrial septal defect [PDF]
, 2010 Habib Saadat +5 more
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