Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Maria Tchitchinadze"'
Autor:
Peng Jiang, Stéphane Loyau, Maria Tchitchinadze, Jacques Ropers, Guillaume Jondeau, Martine Jandrot-Perrus
Publikováno v:
PLoS ONE, Vol 10, Iss 6, p e0128744 (2015)
Exposure of platelets to collagen triggers the formation of a platelet clot. Pharmacological agents capable of inhibiting platelet activation by collagen are thus of potential therapeutic interest. Thrombus formation is initiated by the interaction o
Externí odkaz:
https://doaj.org/article/4016dcc6cc734504a4e00a3f98c0fea1
Autor:
Anthony Demolder, Lisa Bianco, Maryanne Caruana, Elena Cervi, Arturo Evangelista, Guillaume Jondeau, Lisa Lauren Buttigieg, Ángela López-Sainz, Elena Montañés Delmás, Alessandro Pini, Anna Sabaté-Rotés, Katalin Szöcs, Maria Tchitchinadze, Gisela Teixidó-Tura, Yskert von Kodolitsch, Laura Muiño-Mosquera, Julie De Backer
Publikováno v:
Scientia
EUROPEAN JOURNAL OF MEDICAL GENETICS
EUROPEAN JOURNAL OF MEDICAL GENETICS
Arrhythmia; Heritable thoracic aortic disease Arritmia; Enfermedad hereditaria de la aorta torácica Arrítmia; Malaltia hereditària de l'aorta toràcica Background Heritable thoracic aortic diseases (HTAD), typically entailing aortic complications,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::800934a2979a9754d52560a4246e2e73
https://hdl.handle.net/11351/8059
https://hdl.handle.net/11351/8059
Autor:
Nadine Hanna, Tiffany Busa, Mélodie Aubart, Bruno Leheup, Laurence Faivre, Maud Langeois, Laurent Gouya, Jacques Ropers, Patrice Bouvagnet, Sophie Dupuis-Girod, Sophie Naudion, Louise Benarroch, Didier Lacombe, Olivier Milleron, Sylvie Odent, Maria Tchitchinadze, Guillaume Jondeau, Catherine Boileau, Pauline Arnaud, Yves Dulac, Thomas Edouard, Laurence Bal
Publikováno v:
Genetics in Medicine
Genetics in Medicine, 2019, 21 (9), pp.2015-2024. ⟨10.1038/s41436-019-0444-y⟩
Genetics in Medicine, 2019, 21 (9), pp.2015-2024. ⟨10.1038/s41436-019-0444-y⟩
International audience; Purpose : Heritable thoracic aortic aneurysms and dissections (hTAAD) are life-threatening complications of well-known syndromic diseases or underdiagnosed nonsyndromic heritable forms (nshTAAD). Both have an autosomal dominan
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⟩
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
Autor:
Olivier, Milleron, Jacques, Ropers, Florence, Arnoult, Claire, Bouleti, Gabriel, Delorme, Maud, Langeois, Maria, Tchitchinadze, Celine, Guien, Christophe, Beroud, Catherine, Boileau, Guillaume, Jondeau
Publikováno v:
Circulation. Cardiovascular imaging. 12(3)
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 evaluated aort
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
Autor:
Maud Langeois, Emmanuel Lansac, Guillaume Jondeau, Olivier Milleron, F. Arnoult, P. Masi, Maria Tchitchinadze, Jean-François Paul, Claire Bouleti
Publikováno v:
Archives of Cardiovascular Diseases Supplements. 11:60
Background The bicuspid aortic valve (BAV) is associated with aortic dilatation (either at the aortic root and/or at the ascending aorta level) and an increased risk of aortic dissection. Dilation of the ascending aorta level may be secondary to aort
Autor:
M. Gouysse, S. Schmitt, Guillaume Jondeau, Claire Bouleti, O. Phalla, Nicoletta Pasi, Olivier Milleron, Maria Tchitchinadze, Y. Moeuf, F. Arnoult
Publikováno v:
Archives of Cardiovascular Diseases Supplements. 11:57
Objectives Dural ectasia is a major criterion for Marfan syndrome (MFS) diagnosis. However, its definition remains fuzzy with studies on small sample size reporting different criteria to differentiate between Marfan and controls. Methods All MFS pati
Autor:
F. Arnoult, Claire Bouleti, Sabine Schmitt, Guillaume Jondeau, Maria Tchitchinadze, Noémie Tencé, Olivier Milleron, Phalla Ou, Florence Nicot, Nicoletta Pasi
Publikováno v:
Journal of the American College of Cardiology. 71:A2064
Autor:
Philippe Aegerter, Guillaume Jondeau, F. Arnoult, Delphine Detaint, Catherine Bouffard, Mathieu Gautier, Florence Tubach, Sylvie Odent, Henri Plauchu, Patrick Collignon, Maria Tchitchinadze, Isabelle Hoffman, Yves Dulac, Catherine Boileau, Laurence Faivre, Marie-Ange Delrue
Publikováno v:
Archives of cardiovascular diseases
Archives of cardiovascular diseases, Elsevier/French Society of Cardiology, 2010, 103 (5), pp.317-25. ⟨10.1016/j.acvd.2010.04.008⟩
Archives of cardiovascular diseases, 2010, 103 (5), pp.317-25. ⟨10.1016/j.acvd.2010.04.008⟩
Archives of cardiovascular diseases, Elsevier/French Society of Cardiology, 2010, 103 (5), pp.317-25. ⟨10.1016/j.acvd.2010.04.008⟩
Archives of cardiovascular diseases, 2010, 103 (5), pp.317-25. ⟨10.1016/j.acvd.2010.04.008⟩
International audience; BACKGROUND: Recent studies have demonstrated that blockade of the angiotensin II type 1 receptor with losartan decreases aortic damage in an animal model of Marfan syndrome (a KI mouse model with a pathogenic mutation in the g
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9bd7c21b3ae7dc30208b0c4bdb369c93
https://www.hal.inserm.fr/inserm-00511671
https://www.hal.inserm.fr/inserm-00511671