Zobrazeno 1 - 10
of 14
pro vyhledávání: '"Adélaïde Richard"'
Autor:
Jean-François Piéchaud, François Godart, Ali Houeijeh, Adélaïde Richard, Floriane Brief, Olivia Domanski, Jean-Benoit Baudelet, Dominique Guimber, Guy Vaksmann
Publikováno v:
Pediatric Cardiology. 43:1681-1687
Background Over the past twenty years, progress of cardiac surgery has been such that actual life expectancy of a patient with congenital heart disease (CHD) approaches that of the average for the general population. The current challenge is no longe
Autor:
Morgane Billotte, Valérie Deken, Sylvie Joriot, Guy Vaksmann, Adélaïde Richard, Ivan Bouzguenda, François Godart, Jean-Benoit Baudelet, Thameur Rakza, Sylvie Nguyen The Tich, Marie-Paule Guillaume
Publikováno v:
European journal of pediatrics. 180(4)
The aim of this study was to evaluate the frequency of neurodevelopmental disorders (NDD) in children with significant congenital heart disease (CHD) and to determine associated factors to NDD and frequency of follow-up in developmental therapies. Tw
Autor:
Adélaïde Richard, Jacky Nizard, Sébastien Hascoët, Louise Benoit, Laurianne Le Gloan, Pascal Amedro, Adeline Basquin, Hugues Lucron, Marielle Gouton, Magalie Ladouceur, Quentin Hauet, Pamela Moceri, Jelena Radojevic
Publikováno v:
Circulation. 135:2444-2447
Survival into adulthood of patients with unrepaired cyanotic congenital heart defects (CHDs) is possible when cyanotic CHDs are deemed unsuitable for radical surgical repair but are compatible with survival. These situations include, for example, com
Publikováno v:
Anesthésie & Réanimation. 2:316-320
Resume Les troubles du rythme cardiaque congenitaux peuvent avoir 2 origines : le syndrome de Wolff-Parkinson-White (WPW) ou une canalopathie. Plusieurs types de tachycardies peuvent survenir chez les patients atteints du syndrome de WPW. La tachycar
Autor:
Pierre Mauran, Ali Houeijeh, Elise Barre, Clément Karsenty, Hélène Bouvaist, Pamela Moceri, Xavier Iriart, Elie Fadel, Adélaïde Richard, Nathalie Souletie, Emmanuelle Fournier, Lauriane Le Gloan, Magalie Ladouceur, Xavier Jaïs, Yvette Bernard, François Godart, Jelena Radojevic, Jérôme Petit, Laurence Iserin, Damien Bonnet, Gilles Bosser, Sébastien Hascoët, Pascal Amedro, Claire Dauphin, Adeline Basquin, Olivier Sitbon, Marc Humbert
Publikováno v:
Archives of cardiovascular diseases
Archives of cardiovascular diseases, Elsevier/French Society of Cardiology, 2017, 110 (5), pp.303-316. ⟨10.1016/j.acvd.2017.01.006⟩
Archives of cardiovascular diseases, Elsevier/French Society of Cardiology, 2017, 110 (5), pp.303-316. ⟨10.1016/j.acvd.2017.01.006⟩
International audience; Background: The relationship between pulmonary arterial hypertension-specific drug therapy (PAH-SDT) and mortality in Eisenmenger syndrome (ES) is controversial.Aims: To investigate outcomes in patients with ES, and their rela
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::baa245138527a43fcf05dbc23fdf54f8
https://hal.umontpellier.fr/hal-01831902/document
https://hal.umontpellier.fr/hal-01831902/document
Autor:
Yvan Bouzgenda, Guy Vaksmann, François Godart, Ali Houeijeh, Jean-Benoit Baudelet, Adélaïde Richard, Olivia Domanski
Publikováno v:
Archives of Cardiovascular Diseases Supplements. 10:278-279
Background Congenitally corrected transposition of the great arteries (ccTGA) is rare congenital heart disease (CHD) with an estimated prevalence of less than 1% among all CHDs. Long time prognosis is dependent on the systemic right ventricule functi
Autor:
Adélaïde Richard, Guy Vaksmann
Publikováno v:
La Presse Médicale. 40:726-731
Coarctation of the aorta accounts for 7% of congenital heart diseases. It is estimated that currently approximatively 10,000 adult patients have been operated on for coarctation in France. Bicuspid aortic valve occurs in more than 50% of patients. On
Autor:
Louise Benoit, L. Le Gloan, Adélaïde Richard, Hugues Lucron, Sébastien Hascoët, Q. Hauet, Pamela Moceri, Jacky Nizard, Pascal Amedro, Jelena Radojevic, Magalie Ladouceur, Marielle Gouton, Adeline Basquin
Publikováno v:
Archives of Cardiovascular Diseases Supplements. 10:134
Background Maternal cyanotic congenital heart disease (CHD) is considered a great maternal and fetal risks during pregnancy, but information on management of these pregnancies are lacking. The purpose of this study was to assess maternal and fetal ou
Autor:
Guy, Vaksmann, Adélaïde, Richard
Publikováno v:
Presse medicale (Paris, France : 1983). 40(7-8)
Coarctation of the aorta accounts for 7% of congenital heart diseases. It is estimated that currently approximatively 10,000 adult patients have been operated on for coarctation in France. Bicuspid aortic valve occurs in more than 50% of patients. On
Publikováno v:
Archives of Cardiovascular Diseases Supplements. 3(1)
Hypoxemia related to interatrial right-to-left shunt may have a significant impact on exercise tolerance. We report here one centre experience in transcatheter closure of interatrial RL shunt. From August 1995 to 2009, 63 consecutive patients (37 fem