Results 131 to 140 of about 96,734 (313)
A Technique for Coronary Artery Reimplantation in Composite Aortic Root Replacement
, 1994 Mazin A.I. Sarsam
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Coronary artery narrowing after aortic root reconstruction with resorcin-formalin glue [PDF]
, 2000 Luigi Martinelli +4 more
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American Journal of Medical Genetics Part A, EarlyView.ABSTRACT Wisconsin syndrome is a very rare genetic condition characterized by coarse facies, prominent nasal tip, bushy high arched/upsweeping eyebrows, and a full/everted lower lip. Deletion of chromosome 3q24q25 region is considered critical for its manifestation.
Pankaj Prasun +2 more
wiley +1 more source
Frame-mounted porcine valve bioprostheses: Preparation during aortic-root dilation
, 1993 M.H. Butterfield +4 more
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American Journal of Medical Genetics Part C: Seminars in Medical Genetics, EarlyView.ABSTRACT Patients with Turner Syndrome (TS) and those exposed to high concentrations of glucocorticoids have a number of characteristics in common, including an increased risk of cardiovascular disease. Pediatric TS patients underwent studies of salivary cortisol (SC) and cortisone (SCn), body composition, continuous glucose monitoring, vascular ...
Lily Jones +6 more
wiley +1 more source
The role of atrial vessels in aortic root and mitral valve operations [PDF]
, 2000 Gustavo Abuin +3 more
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American Journal of Medical Genetics Part C: Seminars in Medical Genetics, EarlyView.ABSTRACT Turner syndrome (TS) is frequently complicated by congenital heart disease (CHD). While left‐sided lesions such as bicuspid aortic valve (BAV) and coarctation of the aorta are the most common structural heart lesions in TS, other anomalies, such as aortic arch malformations, hypoplastic left heart syndrome (HLHS), persistent left superior vena
Katya de Groote +9 more
wiley +1 more source
A new technique for sparing the aortic valve in patients with aneurysm of the ascending aorta and root [PDF]
, 2000 Ulrik Hvass
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American Journal of Medical Genetics Part C: Seminars in Medical Genetics, EarlyView.ABSTRACT It is evident that Turner syndrome (TS) impacts almost all developmental stages of the fetal heart with congenital heart disease (CHD) being seen in 23%–50% of individuals. Although the spectrum of CHDs in TS is well‐established, with left‐sided lesions predominating, the influence of specific karyotypes on the prevalence and types of CHDs ...
Francisco Álvarez‐Nava +5 more
wiley +1 more source
Aortic root replacement with coronary button reimplantation [PDF]
, 2000 Paul P. Urbanski
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