Zobrazeno 1 - 10
of 16
pro vyhledávání: '"Quentin Hauet"'
Autor:
Céline Grunenwald Gronier, Nadir Benbrik, Bénédicte Romefort, Solène Prigent, Quentin Hauet, Alban-Elouen Baruteau
Publikováno v:
International Journal of Cardiology Congenital Heart Disease, Vol 7, Iss , Pp 100316- (2022)
Background: Device PDA closure is increasingly used in smaller patients. Major safety concerns remain when applied to
Externí odkaz:
https://doaj.org/article/ed1ec2badc74472eb33a5fe0418f09fc
Autor:
Marine Tortigue, Lynne E. Nield, Matilde Karakachoff, Christopher J. McLeod, Emre Belli, Sonya V. Babu-Narayan, Solène Prigent, Angèle Boet, Miriam Conway, Robert W. Elder, Magalie Ladouceur, Paul Khairy, Ewa Kowalik, David M. Kalfa, David J. Barron, Shafi Mussa, Anita Hiippala, Joel Temple, Sylvia Abadir, Laurianne Le Gloan, Matthias Lachaud, Shubhayan Sanatani, Jean-Benoit Thambo, Céline Grunenwald Gronier, Pascal Amedro, Guy Vaksmann, Anne Charbonneau, Linda Koutbi, Caroline Ovaert, Ali Houeijeh, Nicolas Combes, Philippe Maury, Guillaume Duthoit, Bérengère Hiel, Christopher C. Erickson, Caroline Bonnet, George F. Van Hare, Christian Dina, Clément Karsenty, Emmanuelle Fournier, Mathieu Le Bloa, Robert H. Pass, Leonardo Liberman, Juha-Matti Happonen, James C. Perry, Bénédicte Romefort, Nadir Benbrik, Quentin Hauet, Alain Fraisse, Michael A. Gatzoulis, Dominic J. Abrams, Anne M. Dubin, Siew Yen Ho, Richard Redon, Emile A. Bacha, Jean-Jacques Schott, Alban-Elouen Baruteau
Publikováno v:
Circulation: Genomic and Precision Medicine
Circulation: Genomic and Precision Medicine, 2022, 15 (3), ⟨10.1161/CIRCGEN.121.003464⟩
Circulation: Genomic and Precision Medicine, 2022, 15 (3), ⟨10.1161/CIRCGEN.121.003464⟩
Background: Congenitally corrected transposition of the great arteries (ccTGA) is a rare disease of unknown cause. We aimed to better understand familial recurrence patterns. Methods: An international, multicentre, retrospective cohort study was cond
Publikováno v:
Pediatric cardiologyReference. 43(2)
Isoproterenol stress test during cardiac catheterization unmasked dynamic bulbo-ventricular foramen restriction in a 5-year-old boy with bidirectional Glenn anastomosis for tricuspid atresia/transposed great arteries and unexplained syncope.
Autor:
Damien Bonnet, Ali Houeijeh, Gilles Bosser, Clément Karsenty, Pamela Moceri, Pauline Helms, Lisa Guirgis, Elise Barre, Quentin Hauet, Sébastien Hascoët, Khaled Hadeed, Virginie Lambert, Xavier Iriart, Nicolas Pangaud, Bérangère Urbina-Hiel, Meriem Mostefa-Kara, Charlotte Denis, Eric Hery, Zakaria Jalal, Nadir Benbrik, Pierre Mauran, Pascale Maragnes, Hugues Lucron, Pascal Amedro, Céline Gronier, Francisco investigators, Magalie Ladouceur, Stéphanie Douchin, François Godart, Bruno Lefort, Karine Warin Fresse, Jean Benoit Thambo, Maurice Guirgis, Diala Khraiche, Adeline Basquin, Daniela Laux, Ronan Bonefoy, Estibaliz Valdeolmillos, Ivan Bouzguenda, Caroline Ovaert, Antoine Legendre, Laurence Iserin, Samir Harchaoui, Laurence Cohen, Jean Marc Lupoglazoff, Bertrand Leobon, Anne-Sophie Leborgne, Carine Vastel, Aurélie Chalard, Nicolas Combes, Alban-Elouen Baruteau, Hélène Ansquer, Guy Vaksmann, Lucile Houyel, Claire Bertail
Publikováno v:
Cardiology in the Young
Cardiology in the Young, Cambridge University Press (CUP), In press, pp.1-6. ⟨10.1017/S1047951121002717⟩
Cardiology in the Young, Cambridge University Press (CUP), In press, pp.1-6. ⟨10.1017/S1047951121002717⟩
The long-term prospective multi-centre nationwide (French) observational study FRANCISCO will provide new information on perimembranous ventricular septal defect with left ventricular overload but no pulmonary hypertension in children older than 1 ye
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d3e2da9d4e9bef2ce544b51a5047a27c
https://hal.archives-ouvertes.fr/hal-03353802
https://hal.archives-ouvertes.fr/hal-03353802
Autor:
Christophe Deligny, Francois Barriere, P. Orquevaux, Eric Hachulla, Olivier Fain, Delphine Le Mercier, Philippe Ravaud, Jérôme Le Bidois, Bénédicte Romefort, Sophie Georgin-Lavialle, Claire Le Jeunne, Gaëlle Guettrot-Imbert, Francois Sassolas, Elisabeth Villain, Luc Mouthon, Nathalie Costedoat-Chalumeau, Laurent Fermont, Alice Maltret, Quentin Hauet, Mohamed Hamidou, Jean-Charles Piette, Gabriel Baron, Kateri Levesque, Damien Bonnet, Arnaud Theulin, Nathalie Morel
Publikováno v:
International Journal of Cardiology. 248:263-269
Background Dilated cardiomyopathy (DCM), a well-known complication of cardiac neonatal lupus, is associated with high mortality rate. Its risk factors remain unclear. Methods We analyzed occurrence of postnatal DCM among children with high-degree con
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
Autor:
Cyril Flamant, Quentin Hauet, Laura Bourgoin, Hélène Basset, Véronique Gournay, Cecile Cipierre, Géraldine Gascoin, Jean-Christophe Rozé
Publikováno v:
Neonatology
Neonatology, Karger, 2016, 109 (2), pp.139-146. ⟨10.1159/000442278⟩
Neonatology, Karger, 2016, 109 (2), pp.139-146. ⟨10.1159/000442278⟩
Background: Patent ductus arteriosus (PDA) is a condition frequently found in very preterm infants, and its treatment remains a subject of debate. Furthermore, there are only a few studies available that have examined the impact of these treatments o
Autor:
Patricia Teixeira, Lin Li, Atalia Shtorch-Asor, Mara Santos Córdoba, Quentin Hauet, Marcos L.M. Morris, Albert David, Bertrand Isidor, Xuan Huang, Cristina T.N. Medina, Nicolas Joram, Qun Fang, Yanmin Luo, Iris Ferrari, Reuven Sharony, Jayarama S. Kadandale, Olivier Baron, Deenadayalu Anuradha, Ido Laish, Shaobin Lin, Linhuan Huang, Tal Biron-Shental, Laurianne Le Gloan, Chloé Arfeuille, Pauline Arnaud, Maria Gisele dos Santos, Ambika Srikanth, Chandra R Samuel, Faruk Hadziselimovic, Beatriz R. Versiani, Dana Sadeh-Mestechkin, Nadine Hanna, Pooja S. Kulshreshtha, Catherine Boileau, Juliana F. Mazzeu, Meirav Keiser, Satz Mengensatzproduktion, Bénédicte Romefort, Martin Poot, Druckerei Stückle, José Eduardo Baroneza, Aliza Amiel, Aswini Sivasankaran, Ana Carolina S. Fonseca, Véronique Gournay, Silviene Fabiana de Oliveira, Erika L. Freitas, Nadir Benbrik, Liege L. Roese, Carla Rosenberg, Aline Pic-Taylor
Publikováno v:
Molecular Syndromology. 6:I-VI
Autor:
Qun Fang, Bertrand Isidor, Catherine Boileau, Juliana F. Mazzeu, Meirav Keiser, Dana Sadeh-Mestechkin, Cristina T.N. Medina, Nadine Hanna, Pooja S. Kulshreshtha, Erika L. Freitas, Bénédicte Romefort, Quentin Hauet, Olivier Baron, Ambika Srikanth, Tal Biron-Shental, Reuven Sharony, Atalia Shtorch-Asor, Laurianne Le Gloan, Deenadayalu Anuradha, Xuan Huang, Mara Santos Córdoba, Marcos L.M. Morris, Martin Poot, Satz Mengensatzproduktion, Chandra R Samuel, Shaobin Lin, José Eduardo Baroneza, Aliza Amiel, Chloé Arfeuille, Jayarama S. Kadandale, Albert David, Silviene Fabiana de Oliveira, Patricia Teixeira, Iris Ferrari, Carla Rosenberg, Liege L. Roese, Lin Li, Maria Gisele dos Santos, Linhuan Huang, Aswini Sivasankaran, Ana Carolina S. Fonseca, Aline Pic-Taylor, Druckerei Stückle, Yanmin Luo, Faruk Hadziselimovic, Pauline Arnaud, Véronique Gournay, Beatriz R. Versiani, Nadir Benbrik, Ido Laish, Nicolas Joram
Publikováno v:
Molecular Syndromology. 6:304-335
Autor:
Pierre Lindenbaum, Marta Sanchez-Castro, Richard Redon, Christian Dina, Véronique Gournay, Damien Bonnet, Olivier Pichon, Cédric Le Caignec, Hadja Eldjouzi, Philippe Pezard, Eric Charpentier, Quentin Hauet, Cécile Pascal, Béatrice Delasalle-Guyomarch, Adrien Baudry, Jean-Jacques Schott, Pierre-François Busson, Bruno Lefort, Fanny Bajolle
Publikováno v:
Circulation. Cardiovascular Genetics
Circulation. Cardiovascular Genetics, 2016, Equipe 3 Equipe 4, 9 (1), pp.86--94. ⟨10.1161/CIRCGENETICS.115.001213⟩
Circulation. Cardiovascular Genetics, 2016, Equipe 3 Equipe 4, 9 (1), pp.86--94. ⟨10.1161/CIRCGENETICS.115.001213⟩
Background— Congenital heart defects are the most frequent malformations among newborns and a frequent cause of morbidity and mortality. Although genetic variation contributes to congenital heart defects, their precise molecular bases remain unknow
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5ed886bb0b60d5b70f1ce37347c7fc85
https://hal.archives-ouvertes.fr/hal-01831746
https://hal.archives-ouvertes.fr/hal-01831746