Zobrazeno 1 - 10
of 23
pro vyhledávání: '"P R, Vouhé"'
Publikováno v:
Archives des maladies du coeur et des vaisseaux. 100(5)
To assess the cellular and histological basis of irreversible pulmonary hypertension (PHT) in the clinical setting of congenital heart disease (CHD).Although many children with CHD develop pulmonary vascular disease, it is unclear why this complicati
Publikováno v:
Archives des maladies du coeur et des vaisseaux. 97(5)
We retrospectively analyzed the pulmonary biopsies of a Fontan intervention in order to identify predictive markers of its result. The pulmonary biopsies of 17 patients who benefited from the Fontan intervention and 6 controls were studied. The histo
Autor:
P R, Vouhé
Publikováno v:
The Journal of heart valve disease. 5
Autor:
P R, Vouhé, D, Sidi
Publikováno v:
Annales de pediatrie. 39(10)
Publikováno v:
Archives des maladies du coeur et des vaisseaux. 83(12)
Ten of 1,025 patients undergoing coronary bypass surgery received one or two bovine internal mammary artery grafts. Surgery consisted in quadruple coronary bypass in 1 case, triple coronary bypass in 3 cases and double coronary bypass in 6 cases usin
Publikováno v:
The Journal of thoracic and cardiovascular surgery. 99(3)
From June 1983 to April 1988, 100 consecutive infants with symptomatic tetralogy of Fallot (without pulmonary atresia) were operated on. Ages ranged from 0.5 to 12 months (mean 7.3 +/- 3.7). Twenty patients were 0.5 to 3 months, 21 were 3 to 6 months
Publikováno v:
The Journal of thoracic and cardiovascular surgery. 90(3)
Two cases of a very uncommon congenital association (cor triatriatum and total anomalous pulmonary venous connection) are presented. This association should be suspected in any infant with signs of pulmonary venous obstruction.
Publikováno v:
The Journal of thoracic and cardiovascular surgery. 82(4)
Autor:
P R, Vouhé, F, Trinquet, Y, Lecompte, F, Vernant, P M, Roux, G, Touati, G, Pome, F, Leca, J Y, Neveux
Publikováno v:
The Journal of thoracic and cardiovascular surgery. 96(4)
Between 1980 and 1986, 80 infants (less than or equal to 3 months old) with symptomatic aortic coarctation and associated severe tubular hypoplasia of the transverse aortic arch underwent surgical treatment. Extended end-to-end aortic arch anastomosi
Publikováno v:
Archives des maladies du coeur et des vaisseaux. 76(11)
Eighty three patients aged 7 to 74 years underwent 92 repeat valve replacement procedures on one or more valve prostheses (100 repeated valve replacements). Reoperation was performed for: dysfunction of a mechanical prosthesis (21%), degeneration of