Results 171 to 180 of about 48,225 (279)

Transcatheter Atrial Septal Defect Closure Before Versus After Adulthood

open access: diamond, 2022
Mohamed Saber Hafez   +2 more
openalex   +2 more sources

Effects of Intraoperative Ventilation Strategies on Ventilation Inhomogeneity and Inflammatory Response in Pediatric Cardiac Surgery—A Randomized Pilot Study

open access: yesPediatric Anesthesia, Volume 36, Issue 1, Page 88-99, January 2026.
ABSTRACT Background Respiratory arrest during cardiopulmonary bypass (CPB) in pediatric cardiac surgery risks lung dysfunction including derecruitment, atelectasis, and inflammation. Continuous positive airway pressure (CPAP) and lung‐protective ventilation (LPV) during aortic cross‐clamping show inconsistent results in mitigating these risks.
Charlotte Billstein   +7 more
wiley   +1 more source

Atrial Septal Defect [PDF]

open access: yesProceedings of the Royal Society of Medicine, 1942
openaire   +1 more source

Tackling Atrial Septal Defects in Adults

open access: diamond, 2022
Norihisa Toh   +4 more
openalex   +2 more sources

Hope in Miniature: The First Case of Implantation of a “Tiny Pacemaker” in Italy as a Successful Treatment for Congenital Atrioventricular Block in a Low Birth Weight Child

open access: yesCase Reports in Cardiology, Volume 2026, Issue 1, 2026.
Congenital complete atrioventricular block (CAVB) is a rare cardiac condition occurring in approximately one in 15,000 to one in 22,000 live births. Maternal autoimmune diseases, with anti‐ssA (Ro) and anti‐ssB (La) antibodies implicated in 56%–90% of cases, are primary causes.
Ferrari Paola   +5 more
wiley   +1 more source

Pregnancy outcome in women with atrial septal defect: associated with in vitro fertilisation and pre-eclampsia [PDF]

open access: gold, 2019
Sebastian Udholm   +4 more
openalex   +1 more source

Syndromic Congenital Heart Disease Diagnosed in Adulthood: A Reminder of the Phenotypic Variability of Alagille Syndrome

open access: yesCase Reports in Cardiology, Volume 2026, Issue 1, 2026.
Alagille syndrome is a rare multisystemic genetic condition most commonly associated with neonatal liver disease. Variable expressivity is a defining feature of Alagille syndrome, resulting in a broad spectrum of phenotypic variation among individuals who meet the diagnostic criteria. We present an atypical case of cardiac‐predominant Alagille syndrome
Matthew K. Campbell   +4 more
wiley   +1 more source

Home - About - Disclaimer - Privacy