Results 71 to 80 of about 76,255 (251)

First description of partial atrioventricular septal defect in a rabbit [PDF]

, 2018
Congenital heart diseases have rarely been described in rabbits. The purpose of the present case report is to describe the clinical, radiographic, echocardiographic, and pathological features of a partial atrioventricular septal defect in a pet rabbit. A
Baron Toaldo, Marco, Marco Baron Toaldo, Toaldo, Marco Baron, Annalisa Nicoletti, Spattini, Giliola, Palmieri, Chiara, Zeyen, Ulrich, Paolo Selleri, Di Girolamo, Nicola, Ulrich Zeyen, Selleri, Paolo, Nicola Di Girolamo, Nicoletti, Annalisa, Giliola Spattini, Chiara Palmieri   +14 more
core   +1 more source

Contemporary outcomes of complete atrioventricular septal defect repair: Analysis of the Society of Thoracic Surgeons Congenital Heart Surgery Database

Journal of Thoracic and Cardiovascular Surgery, 2014
Objective Contemporary outcomes data for complete atrioventricular septal defect (CAVSD) repair are limited. We sought to describe early outcomes of CAVSD repair across a large multicenter cohort, and explore potential associations with patient ...
J. S. St. Louis, Upinder Jodhka, J. Jacobs, Xia He, K. Hill, S. Pasquali, M. Jacobs   +6 more
semanticscholar   +1 more source

Chd4 and ThPOK cooperate to preserve structural and electrophysiological integrity of the adult heart through Sprr1a repression

The FEBS Journal, EarlyView.
Chd4/NuRD and ThPOK cooperate to maintain transcriptional repression and nuclear organization in adult cardiomyocytes. Chd4 loss reduces miR‐150‐5p, relieving repression of Sprr1a, while ThPOK loss further enhances Sprr1a activation, possibly through altered chromatin–lamina interactions.
Fadoua El Abdellaoui‐Soussi, Apolonia Novillo, Rocío Brea, Marta Ysbert, Lorena Cussó, Gonzalo Pizarro‐Sánchez, Manuel Desco, Iván Hernández, Ángel Luis Armesilla, Ignacio Pérez de Castro, Alicia R. Folgueras, Juan Miguel Redondo, Pablo Gómez‐del Arco   +12 more
wiley   +1 more source

Robotic surgery for atrial septal defect closure in a case of Kabuki syndrome

Türk Kardiyoloji Derneği Arşivi, 2017
Summary– Kabuki syndrome is a rare congenital malformation syndrome characterized by mental retardation, skeletal deformities, auditory dysfunction, cardiac defects, and distinctive facial appearance. Although complex cardiovascular malformations present
Burak Onan, Ünal Aydın, Zeynep Kahraman, İhsan Bakır   +3 more
doaj   +1 more source

Understanding atrioventricular septal defect: Anatomoechocardiographic correlation-12

, 2011
Lar septum and the interchordal spaces (asterisks) that create the ventricular septal defect. (B) The two-dimensional echocardiographic 4-chamber image shows the same features as in the anatomic specimen.
Luis Muñoz-Castellanos (39502), Magdalena Kuri-Nivón (39504), Candace Keirns (39505), Nilda Espinola-Zavaleta (39503)   +3 more
core   +1 more source

Dilemmas in atrioventricular septal defect repair

, 2020
This thesis reports upon clinical outcomes of atrioventricular septal defect (AVSD) repair and of left atrioventricular valve (LAVV) replacement in neonates, infants and adults and reports upon outcomes hypoplastic left heart complex (HLHC) repair ...
IJsselhof, Rinske Johanna
core   +1 more source

Cyclin‐dependent kinase 13 is indispensable for normal mouse heart development

Journal of Anatomy, Volume 246, Issue 4, Page 616-630, April 2025.
Congenital heart disease (CHD) is the most common defect in live births. The role of cyclin‐dependent kinase (CDK13) in cardiogenesis and CHD was studied using a transgenic mouse model (Cdk13tm1b) carrying deletion of exons 3 and 4, causing loss of function.
Qazi Waheed‐Ullah, Anna Wilsdon, Aseel Abbad, Sophie Rochette, Frances Bu'Lock, Asma Ali Saed, Marc‐Phillip Hitz, J. David Brook, Siobhan Loughna   +8 more
wiley   +1 more source

The current surgical perspective to repair of atrioventricular septal defect with common atrioventricular junction

, 2010
Atrioventricular septal defect with common atrioventricular junction is a relatively common congenital cardiac malformation. It sometimes presents challenging surgical problems, especially when seen in combination with tetralogy of Fallot.
Anderson, Robert H., Sylvio C. J. Provenzano, Provenzano, Sylvio C. J., Nunn, Graham R., Karl, Tom R., Tom R. Karl, Robert H. Anderson, Graham R. Nunn   +7 more
core   +1 more source

The Evolving Landscape of CHD Genetics: A Contemporary Guide to Genetic Testing and Management

Journal of Paediatrics and Child Health, EarlyView.
ABSTRACT Congenital heart disease (CHD) is the most common birth defect, affecting an estimated 9.4/1000 infants globally. The genetics of CHD is complex, with most cases thought to have multifactorial aetiology, implicating both genetic and environmental factors.
Bridget R. O'Malley, Gary F. Sholler, Janine Smith, Gillian M. Blue   +3 more
wiley   +1 more source

Familial secundum atrial septal defect with dysrhythmia associated with web neck

The Turkish Journal of Pediatrics, 2002
Most cases of atrial septal defect occur sporadically, but a few families have the defect as a genetic abnormality. A family having familial type secundum atrial septal defect with dysrhythmia associated with web neck is reported.
Zübeyir Kiliç, Birsen Uçar, Ferruh Baş, Ener Cağri Dinleyici, Ersin Sari   +4 more
doaj