Results 111 to 120 of about 659,599 (211)
Between January 1991 and June 1993, eleven children with anomalous origin of the left coronary artery from the pulmonary artery underwent direct aortic reimplantation of the left coronary artery at the German Heart Institute Berlin. The patients' ages ranged from 2.5 months to 10.5 years; six were infants.
V, Alexi-Meskishvili +6 more
openaire +2 more sources
Background. 47XYY syndrome is a rare sex chromosome variation characterized by an additional Y chromosome. Most patients with 47XYY karyotype have normal phenotype.
Hanane Latrech +4 more
doaj +1 more source
Underuse of coronary revascularization procedures in patients considered appropriate candidates for revascularization. [PDF]
Background: Ratings by an expert panel of the appropriateness of treatments may offer better guidance for clinical practice than the variable decisions of individual clinicians, yet there have been no prospective studies of clinical outcomes. We compared
Feder, G +9 more
core
Left Main Coronary Stenosis as a Consequence of Bentall Operation: Percutaneous Treatment
A 65-year-old man suffering from ascending aorta aneurysm and atherosclerotic three vessel disease without left main involvement underwent aortic root replacement with coronary ostia reimplantation according to the modified Bentall technique and multiple
Manrico Balbi +2 more
doaj +1 more source
Background An anomalous right coronary artery (RCA) arising from the left coronary sinus with an interarterial/intramural course can cause exertional ischemia and, rarely, sudden death.
Arya Khezrpour +8 more
doaj +1 more source
René Géronimo Favaloro : pioneer of Cardiac Surgery [PDF]
Dr. René G. Favaloro moved to the Cleveland Clinic in 1962 and proceeded to reshape the face of cardiac surgery as we knew it. Together with his colleagues at the Cleveland Clinic, Drs.
Captur, Gabriella
core
Serum YKL-40 levels in patients with coronary artery disease
Atherosclerosis is considered to be an inflammatory disease in which the initial process is the augmented infiltration of monocytes into the vessel wall and their subsequent differentiation from macrophages into lipid-laden foam cells.
ISMAN, Ferruh K. +4 more
core +1 more source
Anomalous left coronary artery from the pulmonary artery (ALCAPA) is a rare congenital heart disease, presenting either in isolation or with other cardiac anomalies.
Anciline George +3 more
doaj +1 more source
BACKGROUND: T-cell-mediated immune responses play important roles in the progression of atherosclerotic disease. Studies have linked various inflammatory biomarkers with the burden of coronary artery calcification, but the significance of T-cell-specific
박성하 +4 more
core +1 more source
Anomalous origin of the Left Coronary Artery from the Pulmonary Artery (ALCAPA), also known as Bland-White-Garland syndrome, is a rare congenital coronary anomaly with an estimated incidence of 1 in 300,000 live births.
Stefan Veljković +9 more
doaj +1 more source

