Results 241 to 250 of about 175,789 (362)

Report of the National Heart, Lung, and Blood Institute Working Group on Research in Adult Congenital Heart Disease

open access: bronze, 2006
Roberta G. Williams   +13 more
openalex   +1 more source

MRI Assessment of Energy Loss Within the Thoracic Aorta and Its Impact on Cardiac Function in Fontan Patients After Aortic Reconstruction

open access: yesJournal of Magnetic Resonance Imaging, EarlyView.
ABSTRACT Background In Fontan patients undergoing aortic reconstruction, concerns regarding the impact of aortic function on ventricular function exist. Purpose 4D Flow MRI was used to compare energy loss (EL) within the thoracic aorta in patients with and without aortic reconstruction. Study Type Retrospective case control.
Yujiro Ide   +4 more
wiley   +1 more source

Pregnancy in tetralogy of fallot: When and where

open access: yesInternational Journal of Cardiology Congenital Heart Disease, 2021
Maria Giulia Gagliardi   +2 more
doaj  

Endocarditis in Adult Congenital Heart Disease Patients: Prevention, Recognition, and Management. [PDF]

open access: yesCurr Cardiol Rep
Carvajal V   +5 more
europepmc   +1 more source

Feed fortification strategy impact on the risk of necrotizing enterocolitis in infants with complex congenital heart disease

open access: yesJournal of Pediatric Gastroenterology and Nutrition, EarlyView.
Abstract Objectives Development of necrotizing enterocolitis (NEC) in infants with complex congenital heart disease (CHD) has serious negative clinical outcomes. Unfortified expressed breast milk (EBM) is this high‐risk population's enteral feed of choice. EBM often requires fortification to meet nutritional needs to prevent malnutrition.
Jemma Woodgate   +7 more
wiley   +1 more source

Sacubitril/valsartan is associated with improvements in quality of life in adult congenital heart disease patients with systemic right ventricular failure. [PDF]

open access: yesOpen Heart
Neijenhuis RML   +7 more
europepmc   +1 more source

Porto‐sinusoidal vascular disorder in a pediatric patient with prolidase deficiency: A case report

open access: yesJPGN Reports, EarlyView.
Abstract Prolidase deficiency (PD) is a rare autosomal recessive disorder affecting collagen turnover, leading to diverse clinical manifestations including dermatologic lesions, hepatosplenomegaly, and vascular anomalies. Liver involvement in PD is poorly understood, with few reported cases.
Melissa Castro   +5 more
wiley   +1 more source

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