Results 31 to 40 of about 355,187 (399)

Oxygen Availability in Respiratory Muscles During Exercise in Children Following Fontan Operation

open access: yesFrontiers in Pediatrics, 2019
Introduction: As survival of previously considered as lethal congenital heart disease forms is the case in our days, issues regarding quality of life including sport and daily activities emerge.
Fabian Stöcker   +6 more
doaj   +1 more source

Intraindividual validation of 4D flow measurement against 2D flow measurements in complex flow patterns in routine clinical cardiovascular magnetic resonance of bicuspid aortic valve

open access: yesThe Egyptian Journal of Radiology and Nuclear Medicine, 2020
Background Comparing four-dimensional flow against two-dimensional flow measurements in patients with complex flow pattern is still lacking. This study aimed to compare four-dimensional against the two-dimensional flow measurement in patients with ...
Ahmed Kharabish   +7 more
doaj   +1 more source

A Biobank for Long-term and Sustainable Research in the Field of Congenital Heart Disease in Germany

open access: yesGenomics, Proteomics & Bioinformatics, 2016
Congenital heart disease (CHD) is the most frequent birth defect (0.8%–1% of all live births). Due to the advance in prenatal and postnatal early diagnosis and treatment, more than 90% of these patients survive into adulthood today. However, several mid-
Thomas Pickardt   +3 more
doaj   +1 more source

Dynamic Views of Structure and Function during Heart Morphogenesis [PDF]

open access: yes, 2006
Congenital heart defects remain the most common birth defect in humans, occurring in over 1% of live births. The high prevalence of cardiac malformations can be partially attributed to limited knowledge regarding the embryonic roots of the disease.
Forouhar, Arian Soroush
core   +1 more source

Transition in Patients with Congenital Heart Disease in Germany: Results of a Nationwide Patient Survey

open access: yesFrontiers in Pediatrics, 2017
BackgroundA growing number of adults with congenital heart disease (ACHD) pose a particular challenge for health care systems across the world. Upon turning into 18 years, under the German national health care system, ACHD patients are required to switch
Paul C. Helm   +13 more
doaj   +1 more source

Transcatheter Closure of Patent Ductus Arteriosus in Elderly Patients: Initial and One-Year Follow-Up Results—Do We Have the Proper Device?

open access: yesJournal of Interventional Cardiology, 2020
Objectives. Patent ductus arteriosus (PDA) in elderly patients is an uncommon anomaly, and the duct itself is often calcified and fragile; therefore, transcatheter closure is more difficult.
Michal Galeczka   +6 more
doaj   +1 more source

Genetic Diagnostics Contribute to the Risk Stratification for Major Arrhythmic Events in Pediatric Patients with Long QT Syndrome Type 1–3

open access: yesCardiogenetics, 2022
Long QT syndrome (LQTS) is an inherited arrhythmic disorder associated with sudden cardiac death (SCD). This study aimed to identify the clinical and molecular genetic risk factors that contribute to major arrhythmic events (MAEs) in patients with ...
Tobias Burkard   +5 more
doaj   +1 more source

Prenatal diagnosis and prevalence of critical congenital heart defects: an international retrospective cohort study

open access: yesBMJ Open, 2019
Objectives To assess international trends and patterns of prenatal diagnosis of critical congenital heart defects (CCHDs) and their relation to total and live birth CCHD prevalence and mortality.
M. Bakker   +19 more
semanticscholar   +1 more source

Congenital heart defects in IVF/ICSI pregnancy: systematic review and meta‐analysis

open access: yesUltrasound in Obstetrics and Gynecology, 2018
There is no consensus in current practice guidelines on whether conception by in-vitro fertilization (IVF)/intracytoplasmic sperm injection (ICSI) techniques is an indication for performing a fetal echocardiogram.
V. Giorgione   +8 more
semanticscholar   +1 more source

New Insights into the Education of Children with Congenital Heart Disease with and without Trisomy 21

open access: yesMedicina, 2023
Background and Objectives: Patients with congenital heart disease (CHD), especially as a concomitant syndromal disease of trisomy 21 (T21), are at risk for impaired neurodevelopment. This can also affect these patients’ education.
Katharina R. L. Schmitt   +8 more
doaj   +1 more source

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