Results 171 to 180 of about 32,621 (266)

Surgical aortic valve replacement etiologies, hemodynamics, and outcomes in 1346 patients from the Malaysian heart centre

open access: yesJournal of Cardiothoracic Surgery
Background This study examined the characteristics and outcomes of surgical aortic valve replacement (SAVR) both isolated and in combination with other cardiac surgery in Malaysia from 2015 to 2021. Methods This was a retrospective study of 1346 patients
Aslannif Roslan   +11 more
doaj   +1 more source

Case Report: TAVI in a Patient with Single Coronary Artery and Bicuspid Valve. [PDF]

open access: yesCase Rep Cardiol, 2020
Bertin M   +3 more
europepmc   +1 more source

Gemella morbillorum endocarditis in a patient with a bicuspid aortic valve. [PDF]

open access: yes, 2010
Infective endocarditis caused by Gemella morbillorum is a very rare occurrence and only a few cases have been reported in the literature so far. We describe a case of G.
Jamil, Bushra   +3 more
core  

Rare complications of infective endocarditis in marfan-like morphotype: diagnosis of multiple mitral valve aneurysms and aortic root abscess using three-dimensional transesophageal echocardiography

open access: yesBMC Cardiovascular Disorders
Mitral valve aneurysm (MVA) is characterized by a saccular outpouching of the mitral leaflet, and it represents a rare condition typically associated with aortic valve endocarditis. Three-Dimensional Transesophageal Echocardiography (3D-TEE) serves as an
Meriem Boumaaz   +5 more
doaj   +1 more source

Bicuspid valve aortopathy is associated with distinct patterns of matrix degradation. [PDF]

open access: yesJ Thorac Cardiovasc Surg, 2020
Chim YH   +6 more
europepmc   +1 more source

Echocardiographic results after repair of incompetent bicuspid aortic valves

open access: bronze, 1995
Reinhard Moidl   +5 more
openalex   +1 more source

Quadricuspid aortic valve: a rare cause of aortic regurgitation and stenosis

open access: yesThe Turkish Journal of Pediatrics, 2008
Quadricuspid aortic valve is a rare congenital condition that occurs not only as an isolated anomaly, but also with other cardiac defects. We describe a 10-year-old boy whose aortic stenosis was diagnosed during infancy.
Selman Vefa Yildirim   +3 more
doaj  

Thrombus formation on a calcific and severely stenotic bicuspid aortic valve

open access: bronze, 1997
Song Wan   +3 more
openalex   +1 more source

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