Results 11 to 20 of about 50,956 (387)

Clinical implications of the biomechanics of bicuspid aortic valve and bicuspid aortopathy

open access: yesFrontiers in Cardiovascular Medicine, 2022
Bicuspid aortic valve (BAV), which affects up to 2% of the general population, results from the abnormal fusion of the cusps of the aortic valve. Patients with BAV are at a higher risk for developing aortic dilatation, a condition known as bicuspid ...
Ali Fatehi Hassanabad   +9 more
doaj   +4 more sources

A technique for bicuspidization of the aortic valve [PDF]

open access: yesThe Journal of Thoracic and Cardiovascular Surgery, 1959
Although there are a dozen or more etiologies for aortic insufficiency, the ultimate problem is similar in most cases. There is a disparity between the area of the aortic orifice and the area of valve leaflet with which this orifice must be covered during diastole.
CRUZAT, EP   +3 more
core   +4 more sources

International consensus statement on nomenclature and classification of the congenital bicuspid aortic valve and its aortopathy, for clinical, surgical, interventional and research purposes.

open access: yesEuropean Journal of Cardio-Thoracic Surgery, 2021
This International Consensus Classification and Nomenclature for the congenital bicuspid aortic valve condition recognizes 3 types of bicuspid valves: 1.
H. Michelena   +50 more
semanticscholar   +2 more sources

Bicuspid aortic valve [PDF]

open access: yesAnnals of Cardiothoracic Surgery, 2017
Bicuspid aortic valve (BAV) has a prevalence of 0.5–1.39% in the general population. The prevalence of BAV in aortic dissection is 3.5–11.8%. Unfortunately, the incidence of aortic dissection in BAV remains unknown. The etiology of BAV is polygenetic, where environmental factors and unknown genetic factors seem to interact to cause BAV.
Beth Croce   +2 more
openaire   +5 more sources

Bicuspid aortopathy or bicuspid aortopathies? The risk in generalizing [PDF]

open access: yesThe Journal of Thoracic and Cardiovascular Surgery, 2008
n ...
DELLA CORTE, Alessandro, COTRUFO M.
openaire   +4 more sources

Prevalence of Bicuspid Aortic Valve and Associated Aortopathy in Newborns in Copenhagen, Denmark.

open access: yesJournal of the American Medical Association (JAMA), 2021
Importance The prevalence and characteristics of bicuspid aortic valve (BAV) are mainly reported from selected cohorts. BAV is associated with aortopathy, but it is unclear if it represents a fetal developmental defect or is secondary to abnormal valve ...
A. Sillesen   +10 more
semanticscholar   +1 more source

Three-year outcomes of transcatheter aortic valve implantation for bicuspid versus tricuspid aortic stenosis.

open access: yesEuroIntervention, 2022
BACKGROUND Transcatheter aortic valve implantation (TAVI) might be a feasible treatment option for more patients with bicuspid aortic valve (BAV) stenosis. However, long-term follow-up data in this population are scarce.
Dao Zhou   +17 more
semanticscholar   +1 more source

Elucidation of the genetic causes of bicuspid aortic valve disease

open access: yesCardiovascular Research, 2022
Aims The present study aims to characterize the genetic risk architecture of bicuspid aortic valve (BAV) disease, the most common congenital heart defect.
J. Gehlen   +58 more
semanticscholar   +1 more source

Safety and Efficacy of Myval Implantation in Patients with Severe Bicuspid Aortic Valve Stenosis—A Multicenter Real-World Experience

open access: yesJournal of Clinical Medicine, 2022
Bicuspid aortic valve (BAV) is the most common valvular congenital anomaly and is apparent in nearly 50% of candidates for AV replacement. While transcatheter aortic valve implantation (TAVI) is a recommended treatment for patients with symptomatic ...
Ahmad El-Koumy   +19 more
semanticscholar   +1 more source

A Human Hereditary Cardiomyopathy Shares a Genetic Substrate With Bicuspid Aortic Valve

open access: yesCirculation, 2022
Background: The complex genetics underlying human cardiac disease is evidenced by its heterogenous manifestation, multigenic basis, and sporadic occurrence. These features have hampered disease modeling and mechanistic understanding. Here, we show that 2
M. Siguero-Álvarez   +28 more
semanticscholar   +1 more source

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