Results 1 to 10 of about 56,904 (167)

Ascending aortic replacement versus aortic root replacement in patients with type A aortic dissection involving the aortic root. [PDF]

open access: yesTher Adv Cardiovasc Dis
Background: Extensive surgical resection of the thoracic aorta in patients with type A aortic dissection (TAAD) is thought to reduce the risk of late aortic wall degeneration and the need for repeat aortic operations.
Biancari F   +25 more
europepmc   +2 more sources

Growth of the aortic root in children and young adults with Marfan syndrome

open access: yesOpen Heart, 2022
Objectives The primary aim was to gain insight into the growth of the aortic root in children and young adults with Marfan syndrome (MFS). Furthermore, we aimed to identify a clinical profile of patients with MFS who require an aortic root replacement at
Gerard Pals   +8 more
doaj   +1 more source

Magnetic resonance angiography derived predictors of progressive dilatation and surgery of the aortic root in Marfan syndrome.

open access: yesPLoS ONE, 2022
BackgroundTo identify magnetic resonance (MR) angiography derived predictors of progressive dilatation and surgery of the aortic root in Marfan syndrome.Material and methodsWe retrospectively included 111 patients (32.7±16.5 years, range: 7-75 years ...
Julius Matthias Weinrich   +9 more
doaj   +1 more source

Changes in aortic root dimensions after ascending aortic repair with concomitant aortic valve replacement

open access: yesРоссийский кардиологический журнал, 2023
The issue of ascending aortic repair with concomitant aortic valve replacement in pa-tients with ascending aortic aneurysm (AscAA) and aortic valve stenosis is still debatable.Aim.
D. S. Panfilov   +6 more
doaj   +1 more source

Evaluation of aortic root dilation in adult patients after repair of tetralogy of Fallot

open access: yesResearch in Cardiovascular Medicine, 2022
Background and Aim: Aortic root dilation is one of the common complications in patients with a history of tetralogy of Fallot total correction (TFTC).
Mozhgan Parsaee   +5 more
doaj   +1 more source

Valve-Sparing Operation in Patients with Aortic Root Aneurysm

open access: yesУкраїнський журнал серцево-судинної хірургії, 2020
Background. Aortic root aneurysm is rare but life-threatening disease which affects not only aortic wall, but aortic valve as well. Valve-sparing operation was developed by Tirone David and gave a chance to save native aortic valve in patients with ...
A. S. Tsvyk   +4 more
doaj   +1 more source

Biomechanical properties of the aortic root are distinct from those of the ascending aorta in both normal and aneurysmal statesCentral MessagePerspective

open access: yesJTCVS Open, 2023
Background: Although aneurysms of the ascending aorta and the aortic root are treated similarly in clinical guidelines, how biomechanical properties differ between these 2 segments of aorta is poorly defined.
Jennifer C.-Y. Chung, MD, MSc   +7 more
doaj   +1 more source

The association between cardiac magnetic resonance-derived aortic stiffness parameters and aortic dilation in young adults with bicuspid aortic valve: With and without coarctation of aorta

open access: yesAmerican Heart Journal Plus, 2022
Background: Bicuspid aortic valve (BAV) is associated with progressive aortic dilation. Studies in aortopathies have shown a correlation between increased aortic stiffness and aortic dilation.
Vasutakarn Chongthammakun   +6 more
doaj   +1 more source

A SOX17-PDGFB signaling axis regulates aortic root development

open access: yesNature Communications, 2022
Little is known about the developmental causes of aortic root defects. Here the authors show that the inactivation of Sox17 in aortic root endothelium results in aortic root defects affecting aortic valve and coronary ostium.
Pengfei Lu   +17 more
doaj   +1 more source

Aortic Root Dilatation in Children and Adolescents At Al-Hawary General Hospital, & National Benghazi Cardiac Center -Libya

open access: yesمجلة المختار للعلوم, 2021
Isolated dilatation of the aortic root and/or ascending aorta is a rare but well-known cardiovascular manifestation, can be caused by a variety of congenital or acquired conditions; that lead to the weakening of the aortic wall.
Rasmia H. Feituri   +3 more
doaj   +1 more source

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