Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Eleonore Hebbar"'
Autor:
Jerome Soquet, Ali Houeijeh, Marjorie Richardson, Eleonore Hebbar, Guy Vaksmann, Jean‐Benoit Baudelet, Mouhamed Djahoum Moussa, Andre Vincentelli
Publikováno v:
ESC Heart Failure, Vol 9, Iss 5, Pp 3636-3638 (2022)
Abstract A 50‐year‐old female patient was readmitted with refractory systemic right ventricular failure. The patient underwent a Mustard procedure during childhood for transposition of the great arteries. A significant residual ventricular septal
Externí odkaz:
https://doaj.org/article/a4574786561845e4b24499cfe7f7e8ba
Autor:
Emilie Dubois-Deruy, Marie Cuvelliez, Jan Fiedler, Henri Charrier, Paul Mulder, Eleonore Hebbar, Angelika Pfanne, Olivia Beseme, Maggy Chwastyniak, Philippe Amouyel, Vincent Richard, Christophe Bauters, Thomas Thum, Florence Pinet
Publikováno v:
Scientific Reports, Vol 7, Iss 1, Pp 1-10 (2017)
Abstract Although several risk factors such as infarct size have been identified, the progression of heart failure (HF) remains difficult to predict in clinical practice. Using an experimental rat model of post-myocardial infarction (MI), we previous
Externí odkaz:
https://doaj.org/article/64da9270c0a8427f988f904caedd3058
Autor:
Jerome Soquet, Francis Juthier, Agnes Mugnier, Marjorie Richardson, Eleonore Hebbar, Christophe Decoene
Publikováno v:
The Annals of thoracic surgery. 112(3)
Heart transplantation in a recipient with giant left atrium is rare. To correct the mismatch between recipient and donor at the level of the left atrium, plication of the left atrium has been proposed. We report a case in which plication was not feas
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8a5dae3850b09157b7abc4ecaa39ab55
https://pubmed.ncbi.nlm.nih.gov/33497673
https://pubmed.ncbi.nlm.nih.gov/33497673
Autor:
Eleonore Hebbar, Christophe Bauters, Jan Fiedler, Paul Mulder, Philippe Amouyel, Vincent Richard, Florence Pinet, Angelika Pfanne, Maggy Chwastyniak, Thomas Thum, Olivia Beseme, Henri Charrier, Emilie Dubois-Deruy, Marie Cuvelliez
Publikováno v:
Scientific Reports, Vol 8, Iss 1, Pp 1-3 (2018)
A correction to this article has been published and is linked from the HTML and PDF versions of this paper. The error has been fixed in the paper.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4aa7e503fb4ffb53345af71e3c3e2cc1
http://link.springer.com/article/10.1038/s41598-018-35955-7
http://link.springer.com/article/10.1038/s41598-018-35955-7
Autor:
Christophe Bauters, Florence Pinet, Eleonore Hebbar, Paul Mulder, Emilie Dubois-Deruy, Marie Cuvelliez, Henri Charrier, Jan Fiedler, Philippe Amouyel, Thomas Thum, Angelika Pfanne, Olivia Beseme, Vincent Richard, Maggy Chwastyniak
Publikováno v:
Scientific Reports
Scientific Reports, 2017, 7 (1), ⟨10.1038/s41598-017-15011-6⟩
Scientific Reports, Vol 7, Iss 1, Pp 1-10 (2017)
Scientific Reports, Nature Publishing Group, 2017, 7 (1), ⟨10.1038/s41598-017-15011-6⟩
Scientific Reports, 2017, 7 (1), ⟨10.1038/s41598-017-15011-6⟩
Scientific Reports, Vol 7, Iss 1, Pp 1-10 (2017)
Scientific Reports, Nature Publishing Group, 2017, 7 (1), ⟨10.1038/s41598-017-15011-6⟩
Although several risk factors such as infarct size have been identified, the progression of heart failure (HF) remains difficult to predict in clinical practice. Using an experimental rat model of post-myocardial infarction (MI), we previously identi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::411373b53a8833e516ef10e52cce4784
https://hal.science/hal-02267416
https://hal.science/hal-02267416
Autor:
Anne-Frédérique Dessein, Eléonore Hebbar, Joseph Vamecq, Elodie Lebredonchel, Aurore Devos, Jamal Ghoumid, Karine Mention, Dries Dobbelaere, Marie Joncquel Chevalier-Curt, Monique Fontaine, Sabine Defoort, Vassily Smirnov, Claire Douillard, Claire-Marie Dhaenens
Publikováno v:
Molecular Genetics and Metabolism Reports, Vol 31, Iss , Pp 100860- (2022)
Background: Long chain 3-hydroxyacyl-CoA dehydrogenase deficiency (LCHADD) is a rare inherited disease caused by pathogenic variants of HADHA gene. Along with signs common to fatty acid oxidation defects (FAOD), specific retina and heart alterations
Externí odkaz:
https://doaj.org/article/53924885011f4b18a7dac70e488471e0