Results 121 to 130 of about 65,088 (328)

Assessment of intra- and inter-ventricular cardiac dyssynchrony in patients with repaired Tetralogy of Fallot: a cardiac magnetic resonance study [PDF]

open access: yes, 2014
Using radiative magnetohydrodynamic simulations of the magnetized solar photosphere and detailed spectro-polarimetric diagnostics with the Fe I 6301.5 Å and 6302.5 Å photospheric lines in the local thermodynamic equilibrium approximation, we ...
Jing, Linyuan   +8 more
core   +3 more sources

Thoracic Aortic Dissection in Tetralogy of Fallot: A Review of the National Inpatient Sample Database

open access: yesJournal of the American Heart Association : Cardiovascular and Cerebrovascular Disease, 2019
Background Thoracic aortic aneurysm is common in patients with tetralogy of Fallot (TOF); the incidence of thoracic aortic dissection (TAD) is unknown, but generally considered to be uncommon. The purpose of this study was to determine incidence and risk
A. Egbe   +3 more
semanticscholar   +1 more source

Prevalence and Spectrum of Congenital Heart Disease in Individuals With Distal Chromosome 22q11.22–23 Deletions

open access: yesClinical Genetics, EarlyView.
The frequency and severity of congenital heart disease vary extensively in individuals with 22q11.22–23 distal deletions. Reduced gene dosage particularly within the low copy repeat (LCR22) D–E region including MAPK1 and HIC2 conveys risk for these defects.
Tanner J. Nelson   +22 more
wiley   +1 more source

Tetralogy of Fallot in Iceland from 1968 to 2001 [PDF]

open access: yes, 2007
Neðst á síðunni er hægt að nálgast greinina í heild sinni með því að smella á hlekkinn View/OpenObjective: We reviewed our experience regarding tetralogy of Fallot (TOF) in Iceland over a 34 year period from 1968 to 2001.
Gunnlaugur Sigfússon   +2 more
core  

Tetralogy of Fallot: morphological variations and implications for surgical repair

open access: yesEuropean Journal of Cardio-Thoracic Surgery, 2019
OBJECTIVES Tetralogy of Fallot is characterized by anterocephalad deviation of the outlet septum, along with abnormal septoparietal trabeculations, which lead to subpulmonary infundibular stenosis.
Saad M Khan   +7 more
semanticscholar   +1 more source

Associations Between Frailty, Family Functioning, and Quality of Life in Adolescents With Congenital Heart Disease: A Cross‐Sectional Study

open access: yesJournal of Advanced Nursing, EarlyView.
ABSTRACT Aim To examine the relationship between frailty status, family functioning, and quality of life in adolescents with congenital heart disease (CHD). Background Frailty is a rarely assessed health outcome in adolescents. Despite advances in paediatric CHD treatment, potential complications may cause frailty, affecting family dynamics and quality
Chen‐Yan Huang   +7 more
wiley   +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

Patient‐Specific 3‐Dimensional–Bioprinted Model for In Vitro Analysis and Treatment Planning of Pulmonary Artery Atresia in Tetralogy of Fallot and Major Aortopulmonary Collateral Arteries

open access: yesJournal of the American Heart Association : Cardiovascular and Cerebrovascular Disease, 2019
Background Tetralogy of Fallot with major aortopulmonary collateral arteries is a heterogeneous form of pulmonary artery (PA) stenosis that requires multiple forms of intervention. We present a patient‐specific in vitro platform capable of sustained flow
Martin L. Tomov   +4 more
semanticscholar   +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

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