Zobrazeno 1 - 10 of 821 pro vyhledávání: '"G, DELORME"'
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Akademický článek
High prevalence of ventricular repolarization abnormalities in people carrying TGFβR2 mutations
Autor: F. Extramiana, O. Milleron, S. Elbitar, A. Uccellini, M. Langeois, M. Spentchian, G. Delorme, F. Arnoult, I. Denjoy, C. Bouleti, V. Fressart, F. Iserin, P. Maison-Blanche, M. Abifadel, A. Leenhardt, C. Boileau, G. Jondeau
Publikováno v: Scientific Reports, Vol 8, Iss 1, Pp 1-8 (2018)
Abstract Mutations in the TGFβR2 gene have been associated with a life threatening risk of aortic dissection but no arrhythmic death has been previously reported. Two young females carrying a TGFβR2 mutation, initially diagnosed as Marfan syndrome
Externí odkaz: https://doaj.org/article/db8f2e09b007475a9d53422b5a3f6373
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2
Mitral valve prolapse, mitral annular disjunction, left ventricular basal hypertrophy and ventricular repolarization abnormalities in Marfan patients
Autor: C. Delhomme, A. Lasne, O. Milleron, F. Arnoult, G. Delorme, L. Eliahou, N. Ould Ouali, S. Jadoui, F. Extramiana, G. Jondeau
Publikováno v: European Heart Journal. 42
Background Mitral annular disjunction (MAD) is a structural abnormality associated to mitral valve prolapse (MVP). MVP has been associated with malignant ventricular arrhythmia, originating from inferolateral left ventricle (LV) wall. However, the me
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d2a0e9fabbedc9cfb0ed717522af6140
https://doi.org/10.1093/eurheartj/ehab724.1698
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3
Pregnancy in women with bicuspid aortic valve
Autor: N Ould Ouali, G. Delorme, Guillaume Jondeau, F. Arnoult, Ludivine Eliahou, Olivier Milleron, S Belkadi, S Jadoui
Publikováno v: European Heart Journal. 42
Background Aortic dissection during pregnancy is uncommon, however, the risk of aortic dissection is increased if there is underlying aortopathy. Bicuspid aortic valve (BAV) is common in the general population and is associated with the presence of a
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::9a7358ba68a123b40e545cb1b6ddc14b
https://doi.org/10.1093/eurheartj/ehab724.2894
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4
Electrocardiographic and echocardiographic abnormalities associated with mitral valve prolapse in patients with Marfan syndrome
Autor: P Arnaud, C Boileau, N Hanna, O. Milleron, G Delorme, L Eliahou, A. Lasne, B Iung, F Extramiana, G Jondeau, F Arnoult
Publikováno v: Web of Science
Introduction Marfan syndrome (MFS) is responsible for cardiovascular disorders such as aortic aneurism and mitral valve prolapse (MVP). A malignant MVP phenotype combining clinical, electrical and morphological features has been described in symptoma
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cceb9fefea68f24b1fc2e2a7c7c8d541
https://doi.org/10.1093/ehjci/ehaa946.1886
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5
High prevalence of ventricular repolarization abnormalities in people carrying TGFβR2 mutations
Autor: O. Milleron, Fabrice Extramiana, Antoine Leenhardt, Marianne Abifadel, A. Uccellini, Franck Iserin, Claire Bouleti, Catherine Boileau, Maud Langeois, Myrtille Spentchian, Sandy Elbitar, G Delorme, G Jondeau, Véronique Fressart, Isabelle Denjoy, Pierre Maison-Blanche, F Arnoult
Publikováno v: Scientific Reports, Vol 8, Iss 1, Pp 1-8 (2018)
Scientific Reports
Mutations in the TGFβR2 gene have been associated with a life threatening risk of aortic dissection but no arrhythmic death has been previously reported. Two young females carrying a TGFβR2 mutation, initially diagnosed as Marfan syndrome or Loeys
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::00729f0214ad41af0c9f3a84f5d81da5
https://doaj.org/article/db8f2e09b007475a9d53422b5a3f6373
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6
Pathogenic FBN1 Genetic Variation and Aortic Dissection in Patients With Marfan Syndrome
Autor: Guillaume Jondeau, Catherine Boileau, Quentin Pellenc, Jacques Ropers, Celine Guien, Nadine Hanna, G. Delorme, Olivier Milleron, Pauline Arnaud, F. Arnoult, Laurent Gouya, Richard Raffoul, Maria Tchitchinadze, Christophe Béroud, Delphine Detaint, Maud Langeois
Publikováno v: J Am Coll Cardiol
Journal of the American College of Cardiology
Journal of the American College of Cardiology, Elsevier, 2020, 75 (8), pp.843-853. ⟨10.1016/j.jacc.2019.12.043⟩
Journal of the American College of Cardiology, 2020, 75 (8), pp.843-853. ⟨10.1016/j.jacc.2019.12.043⟩
International audience; BackgroundAortic risk has not been evaluated in patients with Marfan syndrome and documented pathogenic variants in the FBN1 gene.ObjectivesThis study sought to describe aortic risk in a population with Marfan syndrome with pa
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a6e5a7c430b2dff05d2510d25c5a0b60
https://pubmed.ncbi.nlm.nih.gov/32130919
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7
Clinical Significance of Aortic Root Modification Associated With Bicuspid Aortic Valve in Marfan Syndrome
Autor: Maria Tchitchinadze, Olivier Milleron, Jacques Ropers, Maud Langeois, Guillaume Jondeau, Christophe Béroud, Claire Bouleti, Catherine Boileau, Celine Guien, G. Delorme, F. Arnoult
Publikováno v: Circulation: Cardiovascular Imaging. 12
Background: Both bicuspid aortic valve (BAV) and Marfan syndrome have been associated with aortic dissection risk, but it is unknown whether the presence of BAV is associated with an increased aortic risk in patients with an FBN1 gene mutation. We ev
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::013f71ae331d24daca09f75a9b8b72df
https://doi.org/10.1161/circimaging.118.008129
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8
Marfan Sartan: a randomized, double-blind, placebo-controlled trial
Autor: H. Plauchu, Francois Sassolas, F. Arnoult, G. Delorme, Florence Tubach, Sophie Naudion, Guillaume Jondeau, Jacques Ropers, Olivier Milleron, Sylvie Odent, Martine Barthelet, Delphine Detaint, Philippe Aegerter, Nicolas Pangaud, Catherine Boileau, Thomas Edouard, Sophie Dupuis-Girod, Gilbert Habib, Jean-Eric Wolf, David Attias, Laurence Faivre, Adeline Basquin, Patrick Collignon, Yves Dulac, Julie Thomas-Chabaneix
Publikováno v: European Heart Journal
European Heart Journal, Oxford University Press (OUP): Policy B, 2015, 36 (32), pp.2160--2166. ⟨10.1093/eurheartj/ehv151⟩
European Heart Journal, 2015, 36 (32), pp.2160--2166. ⟨10.1093/eurheartj/ehv151⟩
AIMS: To evaluate the benefit of adding Losartan to baseline therapy in patients with Marfan syndrome (MFS). METHODS AND RESULTS: A double-blind, randomized, multi-centre, placebo-controlled, add on trial comparing Losartan (50 mg when \textless50 kg
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::83d14e142be409feaf36780e80b55389
https://doi.org/10.1093/eurheartj/ehv151
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9
Clinical, electrical and morphological cardiac disorders in Marfan patients with FBN1 mutations
Autor: F. Arnoult, G. Delorme, Nadine Hanna, Guillaume Jondeau, Olivier Milleron, Pauline Arnaud, Catherine Boileau, Fabrice Extramiana, A. Lasne
Publikováno v: Archives of Cardiovascular Diseases Supplements. 12:99
Introduction Marfan syndrome (MFS) is responsible for cardiovascular disorders such as aortic aneurism and mitral valve prolapse (MVP). A malignant clinical, electrical and morphological MVP phenotype is associated with sudden cardiac death. We studi
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::eb2eea7d80276ed04f68ed9031f737eb
https://doi.org/10.1016/j.acvdsp.2019.09.217
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10
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