Results 31 to 40 of about 141,829 (340)

Atrioventricular canal defect and genetic syndromes: the unifying role of sonic hedgehog [PDF]

open access: yes, 2019
The atrioventricular canal defect (AVCD) is a congenital heart defect (CHD) frequently associated with extracardiac anomalies (75%). Previous observations from a personal series of patients with AVCD and "polydactyly syndromes" showed that the distinct ...
Baban, A   +9 more
core   +1 more source

The anatomy of interatrial communications - what does the interventionist need to know? [PDF]

open access: yes, 2008
Increasingly, the interventional cardiologist is seeking to close interatrial communications by inserting devices by means of catheterisation. So as to optimise these procedures, it is adavantageous to have a firm grasp of the anatomy of the normal ...
Anderson, RH, Martins, JDF
core   +1 more source

Unravelling Atrioventricular Block Risk in Inflammatory Diseases: Systemic Inflammation Acutely Delays Atrioventricular Conduction via a Cytokine‐Mediated Inhibition of Connexin43 Expression

open access: yesJournal of the American Heart Association: Cardiovascular and Cerebrovascular Disease, 2021
Background Recent data suggest that systemic inflammation can negatively affect atrioventricular conduction, regardless of acute cardiac injury.
Pietro Enea Lazzerini   +21 more
doaj   +1 more source

Electrophysiology Study for Complex Supraventricular Tachycardia in Congenital Heart Disease Patients With Single‐Ventricle Physiology

open access: yesJournal of the American Heart Association: Cardiovascular and Cerebrovascular Disease, 2016
BackgroundSupraventricular tachycardia (SVT) is common in complex congenital heart disease (CCHD) patients with single‐ventricle physiology and may cause hemodynamic deterioration.
Shuenn‐Nan Chiu   +5 more
doaj   +1 more source

Fetal heterotaxy with tricuspid atresia, pulmonary atresia, and isomerism of the right atrial appendages at 22 weeks. [PDF]

open access: yes, 2013
We report the accurate prenatal diagnosis at 22 weeks gestation of right atrial isomerism in association with tricuspid atresia. Several distinctive sonographic features of isomerism of the right atrial appendages were present in this fetus: complex ...
Richardson, Randy R   +3 more
core   +2 more sources

Clarifying the atrioventricular junctional anatomy in the setting of double outlet right atrium

open access: yesAnnals of Pediatric Cardiology, 2015
Double outlet atrium is a rare cardiac anomaly wherein one of the atriums, most frequently the right atrium, opens into both the ventricles. Although seen more commonly in the setting of atrioventricular septal defect, this arrangement can also be found ...
Saurabh Kumar Gupta   +3 more
doaj   +1 more source

Rate-dependency of action potential duration and refractoriness in isolated myocytes from the rabbit AV node and atrium [PDF]

open access: yes, 2000
During atrial fibrillation, ventricular rate is determined by atrioventricular nodal (AVN) conduction, which in part is dependent upon the refractoriness of single AVN cells.
Andrew C. Rankin   +48 more
core   +1 more source

Sinus venosus atrial septal defect device closure

open access: yesHeart India
With technical advancements, transcatheter closure of sinus venosus atrial septal defect (SVASD) proves safe and effective, even in developing countries.
G. B Chandra Shekara Reddy   +3 more
doaj   +1 more source

Syncope and paroxysmal atrioventricular block

open access: yesJournal of Arrhythmia, 2017
Current literature reveals three types of paroxysmal atrioventricular block (AVB) that can cause syncope:Intrinsic paroxysmal atrioventricular block is due to an intrinsic disease of the AV conduction system; this type of “cardiac syncope” is also ...
Milena Aste, Michele Brignole
doaj   +1 more source

Assessment of Atrioventricular Septal Defect on Echocardiography

open access: yesJournal of the Indian Academy of Echocardiography & Cardiovascular Imaging, 2020
Atrioventricular septal defect comprise of 1.4-2.9% of congenital cardiac defect and is most common congenital cardiac defect in Trisomy 21. This anomaly is characterized by a common atrioventricular junction coexisting with atrial and/or ventricular ...
Munesh Tomar
doaj   +1 more source

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