Search Results - "DULAC, Yves"

Marfan Sartan: a randomized, double-blind, placebo-controlled trial by Milleron, Olivier, Arnoult, Florence, Ropers, Jacques, Aegerter, Philippe, Detaint, Delphine, Delorme, Gabriel, Attias, David, Tubach, Florence, Dupuis-Girod, Sophie, Plauchu, Henry, Barthelet, Martine, Sassolas, Francois, Pangaud, Nicolas, Naudion, Sophie, Thomas-Chabaneix, Julie, Dulac, Yves, Edouard, Thomas, Wolf, Jean-Eric, Faivre, Laurence, Odent, Sylvie, Basquin, Adeline, Habib, Gilbert, Collignon, Patrick, Boileau, Catherine, Jondeau, Guillaume

“…To evaluate the benefit of adding Losartan to baseline therapy in patients with Marfan syndrome (MFS). A double-blind, randomized, multi-centre,…”
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MFAP5 Loss-of-Function Mutations Underscore the Involvement of Matrix Alteration in the Pathogenesis of Familial Thoracic Aortic Aneurysms and Dissections by Barbier, Mathieu, Gross, Marie-Sylvie, Aubart, Mélodie, Hanna, Nadine, Kessler, Ketty, Guo, Dong-Chuan, Tosolini, Laurent, Ho-Tin-Noe, Benoit, Regalado, Ellen, Varret, Mathilde, Abifadel, Marianne, Milleron, Olivier, Odent, Sylvie, Dupuis-Girod, Sophie, Faivre, Laurence, Edouard, Thomas, Dulac, Yves, Busa, Tiffany, Gouya, Laurent, Milewicz, Dianna M., Jondeau, Guillaume, Boileau, Catherine

“…Thoracic aortic aneurysm and dissection (TAAD) is an autosomal-dominant disorder with major life-threatening complications. The disease displays great genetic…”
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Health-related quality of life in children and adolescents with Marfan syndrome or related disorders: a controlled cross-sectional study by Edouard, Thomas, Picot, Marie-Christine, Bajanca, Fernanda, Huguet, Helena, Guitarte, Aitor, Langeois, Maud, Chesneau, Bertrand, Van Kien, Philippe Khau, Garrigue, Eric, Dulac, Yves, Amedro, Pascal

“…This cross-sectional controlled study aims to assess health-related quality of life (HRQoL) of children and adolescents with a molecular diagnosis of Marfan…”
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The usefulness of 3D printed heart models for medical student education in congenital heart disease by Karsenty, Clement, Guitarte, Aitor, Dulac, Yves, Briot, Jerome, Hascoet, Sebastien, Vincent, Remi, Delepaul, Benoit, Vignaud, Paul, Djeddai, Camelia, Hadeed, Khaled, Acar, Philippe

“…Abstract Background Three-dimensional (3D) printing technology enables the translation of 2-dimensional (2D) medical imaging into a physical replica of a…”
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TAD boundary deletion causes PITX2-related cardiac electrical and structural defects by Baudic, Manon, Murata, Hiroshige, Bosada, Fernanda M., Melo, Uirá Souto, Aizawa, Takanori, Lindenbaum, Pierre, van der Maarel, Lieve E., Guedon, Amaury, Baron, Estelle, Fremy, Enora, Foucal, Adrien, Ishikawa, Taisuke, Ushinohama, Hiroya, Jurgens, Sean J., Choi, Seung Hoan, Kyndt, Florence, Le Scouarnec, Solena, Wakker, Vincent, Thollet, Aurélie, Rajalu, Annabelle, Takaki, Tadashi, Ohno, Seiko, Shimizu, Wataru, Horie, Minoru, Kimura, Takeshi, Ellinor, Patrick T., Petit, Florence, Dulac, Yves, Bru, Paul, Boland, Anne, Deleuze, Jean-François, Redon, Richard, Le Marec, Hervé, Le Tourneau, Thierry, Gourraud, Jean-Baptiste, Yoshida, Yoshinori, Makita, Naomasa, Vieyres, Claude, Makiyama, Takeru, Mundlos, Stephan, Christoffels, Vincent M., Probst, Vincent, Schott, Jean-Jacques, Barc, Julien

“…While 3D chromatin organization in topologically associating domains (TADs) and loops mediating regulatory element-promoter interactions is crucial for…”
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Impact of clinical and genetic findings on the management of young patients with Brugada syndrome by Andorin, Antoine, MD, Behr, Elijah R., MA, MBBS, MD, FRCP, Denjoy, Isabelle, MD, Crotti, Lia, MD, PhD, Dagradi, Federica, MD, Jesel, Laurence, MD, Sacher, Fréderic, MD, Petit, Bertrand, MD, Mabo, Philippe, MD, Maltret, Alice, MD, Wong, Leonie C.H., MD, Degand, Bruno, MD, Bertaux, Géraldine, MD, Maury, Philippe, MD, Dulac, Yves, MD, Delasalle, Béatrice, MS, Gourraud, Jean-Baptiste, MD, PhD, Babuty, Dominique, MD, PhD, Blom, Nico A., MD, PhD, Schwartz, Peter J., MD, Wilde, Arthur A., MD, PhD, Probst, Vincent, MD, PhD

“…Background Brugada syndrome (BrS) is an arrhythmogenic disease associated with sudden cardiac death (SCD) that seldom manifests or is recognized in childhood…”
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Parental mosaicism in Marfan and Ehlers-Danlos syndromes and related disorders by Chesneau, Bertrand, Plancke, Aurélie, Rolland, Guillaume, Chassaing, Nicolas, Coubes, Christine, Brischoux-Boucher, Elise, Edouard, Thomas, Dulac, Yves, Aubert-Mucca, Marion, Lavabre-Bertrand, Thierry, Plaisancié, Julie, Khau Van Kien, Philippe

“…Marfan syndrome (MFS) is a heritable connective tissue disorder (HCTD) caused by pathogenic variants in FBN1 that frequently occur de novo. Although…”
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Impact of a transition education program on health-related quality of life in pediatric patients with congenital heart disease: study design for a randomised controlled trial by Werner, Oscar, Bredy, Charlene, Lavastre, Kathleen, Guillaumont, Sophie, De La Villeon, Gregoire, Vincenti, Marie, Gerl, Cristelle, Dulac, Yves, Souletie, Nathalie, Acar, Philippe, Pages, Laurence, Picot, Marie-Christine, Bourrel, Gerard, Oude Engberink, Agnes, Million, Elodie, Abassi, Hamouda, Amedro, Pascal

“…Recent advances in the field of congenital heart disease (CHD) led to an improved prognosis of the patients and in consequence the growth of a new population:…”
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Health-related quality of life and physical activity in children with inherited cardiac arrhythmia or inherited cardiomyopathy: the prospective multicentre controlled QUALIMYORYTHM study rationale, design and methods by Amedro, Pascal, Werner, Oscar, Abassi, Hamouda, Boisson, Aymeric, Souilla, Luc, Guillaumont, Sophie, Calderon, Johanna, Requirand, Anne, Vincenti, Marie, Pommier, Victor, Matecki, Stefan, De La Villeon, Gregoire, Lavastre, Kathleen, Lacampagne, Alain, Picot, Marie-Christine, Beyler, Constance, Delclaux, Christophe, Dulac, Yves, Guitarte, Aitor, Charron, Philippe, Denjoy-Urbain, Isabelle, Probst, Vincent, Baruteau, Alban-Elouen, Chevalier, Philippe, Di Filippo, Sylvie, Thambo, Jean-Benoit, Bonnet, Damien, Pasquie, Jean-Luc

“…Abstract Background Advances in paediatric cardiology have improved the prognosis of children with inherited cardiac disorders. However, health-related quality…”
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FUTURE-2: Results from an open-label, long-term safety and tolerability extension study using the pediatric FormUlation of bosenTan in pUlmonary arterial hypeRtEnsion by Berger, Rolf M.F, Haworth, Sheila G, Bonnet, Damien, Dulac, Yves, Fraisse, Alain, Galiè, Nazzareno, Ivy, D. Dunbar, Jaïs, Xavier, Miera, Oliver, Rosenzweig, Erika B, Efficace, Michela, Kusic-Pajic, Andjela, Beghetti, Maurice

“…Abstract Background A novel formulation of bosentan was evaluated in children with pulmonary arterial hypertension (PAH) in FUTURE-1, which characterized its…”
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Advancing paediatric cardiac imaging: a comprehensive analysis of the feasibility and accuracy of a novel 3D paediatric transoesophageal probe by Karsenty, Clément, Hadeed, Khaled, Pyra, Pierrick, Guitarte, Aitor, Djeddai, Camelia, Vincent, Remi, Dulac, Yves, Silagdze, Ia, Gobin, Julie, Combes, Nicolas, Ratsimandresy, Miarisoa, Berthomieu, Lionel, Calvaruso, Davide, Acar, Philippe

“…Pediatric transoesophageal echocardiography (TOE) probes have remained two-dimensional (2D) limiting their use compared to adults. While critical in pediatrics…”
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Impact of 3D-printed models in meetings with parents of children undergoing interventional cardiac catheterisation by Karsenty, Clément, Hadeed, Khaled, Djeddai, Camelia, Lateyron, Julie, Guitarte, Aitor, Vincent, Remi, DeBarros, Nathalie, Combes, Nicolas, Briot, Jerome, Dulac, Yves, Yrondi, Antoine, Acar, Philippe

“…Paediatric interventional catheterisation has consistently improved in recent decades, with often highly successful outcomes. However, progress is still…”
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Assessment of Ventricular Septal Defect Size and Morphology by Three-Dimensional Transthoracic Echocardiography by Hadeed, Khaled, MD, Hascoet, Sébastien, MD, Amadieu, Romain, MD, Karsenty, Clément, MD, Cuttone, Fabio, MD, Leobon, Bertrand, MD, PhD, Dulac, Yves, MD, Acar, Philippe, MD, PhD

“…Background Morphologic description of ventricular septal defect (VSD) is mandatory before performing the newly developed transcatheter closure procedure…”
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Outcome of coronary artery bypass grafting performed in young children by Legendre, Antoine, MD, Chantepie, Alain, MD, PhD, Belli, Emre, MD, Vouhé, Pascal R., MD, PhD, Neville, Paul, MD, Dulac, Yves, MD, Vaksmann, Guy, MD, Bonnet, Damien, MD, PhD, Serraf, Alain, MD, PhD

“…Objectives The long-term patency rate of coronary artery bypass grafting for which arterial grafts are used is known to be high in the pediatric population…”
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Effect of Beta-Blockade on Ascending Aortic Dilatation in Children With the Marfan Syndrome by Ladouceur, Magalie, MD, Fermanian, Christophe, PhD, Lupoglazoff, Jean-Marc, MD, Edouard, Thomas, MD, Dulac, Yves, MD, Acar, Philippe, MD, Magnier, Suzel, MD, Jondeau, Guillaume, MD, PhD

“…Aortic root dilatation is the principal life-threatening complication in Marfan syndrome, leading to aortic regurgitation, dissection, and rupture. Beta…”
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A +3 variant at a donor splice site leads to a skipping of the MYH11 exon 32, a recurrent RNA defect causing Heritable Thoracic Aortic Aneurysm and Dissection and/or Patent Ductus Arteriosus by Chesneau, Bertrand, Plancke, Aurélie, Rolland, Guillaume, Marcheix, Bertrand, Dulac, Yves, Edouard, Thomas, Plaisancié, Julie, Aubert‐Mucca, Marion, Julia, Sophie, Langeois, Maud, Lavabre‐Bertrand, Thierry, Khau Van Kien, Philippe

“…Background Pathogenic variants in MYH11 are associated with either heritable thoracic aortic aneurysm and dissection (HTAAD), patent ductus arteriosus (PDA)…”
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Clinical and genetic data of 22 new patients with SMAD3 pathogenic variants and review of the literature by Chesneau, Bertrand, Edouard, Thomas, Dulac, Yves, Colineaux, Hélène, Langeois, Maud, Hanna, Nadine, Boileau, Catherine, Arnaud, Pauline, Chassaing, Nicolas, Julia, Sophie, Jondeau, Guillaume, Plancke, Aurélie, Khau Van Kien, Philippe, Plaisancié, Julie

“…Background Pathogenic SMAD3 variants are responsible for a cardiovascular phenotype, mainly thoracic aortic aneurysms and dissections. Precocious…”
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Corrigendum to “FUTURE-2: Results from an open-label, long-term safety and tolerability extension study using the pediatric FormUlation of bosenTan in pUlmonary arterial hypeRtEnsion” [Int. J. Cardiol. 202 (2016) 52–58] by Berger, Rolf M.F, Haworth, Sheila G, Bonnet, Damien, Dulac, Yves, Fraisse, Alain, Galiè, Nazzareno, Ivy, D. Dunbar, Jaïs, Xavier, Miera, Oliver, Rosenzweig, Erika B, Efficace, Michela, Kusic-Pajic, Andjela, Beghetti, Maurice

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Parental Electrocardiographic Screening Identifies a High Degree of Inheritance for Congenital and Childhood Nonimmune Isolated Atrioventricular Block by BARUTEAU, Alban-Elouen, BEHAGHEL, Albin, GOURNAY, Veronique, ROUAULT, Francis, CHANTEPIE, Alain, GUILLAUMONT, Sophie, GODART, François, MARTINS, Raphael P, DELASALLE, Beatrice, BONNET, Caroline, FRAISSE, Alain, SCHLEICH, Jean-Marc, FOUCHARD, Swanny, LUSSON, Jean-Rene, DULAC, Yves, DAUBERT, Jean-Claude, LE MAREC, Herve, PROBST, Vincent, MABO, Philippe, SCHOTT, Jean-Jacques, DINA, Christian, CHATEL, Stephanie, VILLAIN, Elisabeth, THAMBO, Jean-Benoit, MARCON, François

“…The origin of congenital or childhood nonimmune isolated atrioventricular (AV) block remains unknown. We hypothesized that this conduction abnormality in the…”
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Cardiac strangulation: An atypical complication from epicardial pacemaker leads in a newborn by Tahhan, Nabil, Ba, Papa, Hadeed, Khaled, Dulac, Yves, Cuttone, Fabio, Leobon, Bertrand

“…We report a rare and serious complication of cardiac strangulation arising from the implantation of epicardial pacing leads in a newborn. Patient's follow-up…”
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