Results 61 to 70 of about 173,293,143 (185)

Safety and Utility of Smartphone‐Based Heart Monitors in Pediatric Patients With Cardiovascular Implantable Electronic Devices

open access: yesJournal of Cardiovascular Electrophysiology, EarlyView.
Smartphone heart monitors in pediatric CIEDs: A pilot study. Smartphone heart monitors did not induce EMI in children with CIEDs, enabling reliable heart rate measurement and accurate identification of ventricular non‐captures. ABSTRACT Background Portable heart monitors enable on‐demand electrocardiogram (ECG) recordings and enhance symptom‐rhythm ...
Chun‐Lok Ho   +3 more
wiley   +1 more source

Computed tomography angiography imaging of double superior vena cava in a case of tetralogy of fallot

open access: yesRadiology Case Reports
Tetralogy of Fallot is characterized by ventricular septal defect, right ventricular hypertrophy, overriding of aorta and pulmonary tract obstruction. This leads to the development of cyanosis in the baby.
Achal Gulghane, Msc   +3 more
doaj   +1 more source

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

open access: yesJournal 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   +8 more
wiley   +1 more source

Standardized Reporting of Cardiac Magnetic Resonance Examinations in Children With Cardiac Diseases and Adults With Congenital Heart Disease: A Scientific Statement From the Association for European Pediatric and Congenital Cardiology (AEPC) and the International Society for Magnetic Resonance in Medicine (ISMRM)

open access: yes
Journal of Magnetic Resonance Imaging, EarlyView.
Francesca Raimondi   +26 more
wiley   +1 more source

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

open access: yesJournal 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   +3 more
wiley   +1 more source

A Case of Fallot Tetralogy Admitted for Acute Myocardial Infarction

open access: yes, 2020
We report the rare case of a 43-year-old male with untreated tetralogy of Fallot, admitted for acuteinferior myocardial infarction. The etiology of the myocardial infarction was atherosclerotic heartdisease.
Kudat, Hasan
core  

Long‐term outcomes following modified Blalock–Taussig–Thomas shunt placement in 13 dogs with cyanotic congenital heart disease

open access: yesJournal of Small Animal Practice, EarlyView.
Objectives To describe long‐term outcome and owner‐perceived quality of life in dogs with cyanotic congenital cardiac disease undergoing modified Blalock–Taussig–Thomas shunt procedure. Materials and Methods Medical records of dogs that underwent Blalock–Taussig–Thomas shunt between 2009 and 2025 at a small animal referral hospital were retrospectively
M. Rossanese, J. Hannabuss, D. Brockman
wiley   +1 more source

Nutritional Status of Tetralogy of Fallot Patients at Dr. Hasan Sadikin General Hospital Bandung

open access: yesAlthea Medical Journal, 2016
Background: Undernutrition is common in children with congenital heart disease (CHD), especially in developing countries including Indonesia. The objective of the study was to describe the nutritional status of children patients with Tetralogy of Fallot.
Gabriella Cafrina   +2 more
doaj   +1 more source

Patient-Specific Modeling of Tetralogy of Fallot [PDF]

open access: yes, 2015
Tetralogy of Fallot (TOF) is one of the more complicated types of congenital heart defects. TOF a ects 3-5% of all infants born with congenital heart defects and is a leading cause of cyanosis, which occurs when insu cient amount of oxygen are ...
Dong, Melody
core   +1 more source

Scimitar syndrome with tetralogy of fallot and pulmonary atresia

open access: yesThe Egyptian Heart Journal, 2015
Scimitar syndrome is a rare variant of partial anomalous pulmonary venous connection. The association of Scimitar syndrome with another cardiac congenital anomaly such as tetralogy of Fallot with pulmonary atresia is extremely rare; we are reporting a ...
Sameh R. Ismail   +2 more
doaj   +1 more source

Home - About - Disclaimer - Privacy