Zobrazeno 1 - 10
of 187
pro vyhledávání: '"Isabelle, Denjoy"'
A need for exhaustive and standardized characterization of ion channels activity. The case of KV11.1
Autor:
Malak Alameh, Barbara Ribeiro Oliveira-Mendes, Florence Kyndt, Jordan Rivron, Isabelle Denjoy, Florian Lesage, Jean-Jacques Schott, Michel De Waard, Gildas Loussouarn
Publikováno v:
Frontiers in Physiology, Vol 14 (2023)
hERG, the pore-forming subunit of the rapid component of the delayed rectifier K+ current, plays a key role in ventricular repolarization. Mutations in the KCNH2 gene encoding hERG are associated with several cardiac rhythmic disorders, mainly the Lo
Externí odkaz:
https://doaj.org/article/71b00d18ad514452996f646c5d8d8348
Autor:
Pascal Amedro, Oscar Werner, Hamouda Abassi, Aymeric Boisson, Luc Souilla, Sophie Guillaumont, Johanna Calderon, Anne Requirand, Marie Vincenti, Victor Pommier, Stefan Matecki, Gregoire De La Villeon, Kathleen Lavastre, Alain Lacampagne, Marie-Christine Picot, Constance Beyler, Christophe Delclaux, Yves Dulac, Aitor Guitarte, Philippe Charron, Isabelle Denjoy-Urbain, Vincent Probst, Alban-Elouen Baruteau, Philippe Chevalier, Sylvie Di Filippo, Jean-Benoit Thambo, Damien Bonnet, Jean-Luc Pasquie
Publikováno v:
Health and Quality of Life Outcomes, Vol 19, Iss 1, Pp 1-9 (2021)
Abstract Background Advances in paediatric cardiology have improved the prognosis of children with inherited cardiac disorders. However, health-related quality of life (QoL) and physical activity have been scarcely analysed in children with inherited
Externí odkaz:
https://doaj.org/article/d56b3be256d042baaf62bc952e6d1f50
Autor:
Quentin Plumereau, MSc, Olivier Theriault, PhD, Valérie Pouliot, BSc, Adrien Moreau, PhD, Elodie Morel, PhD, Véronique Fressart, MD, PhD, Isabelle Denjoy, MD, Antoine Delinière, MD, Francis Bessière, MD, Philippe Chevalier, MD, Tamer M. Gamal El-Din, PhD, Mohamed Chahine, PhD
Publikováno v:
CJC Open, Vol 3, Iss 3, Pp 256-266 (2021)
Background: Nav1.5, which is encoded by the SCN5A gene, is the predominant voltage-gated Na+ channel in the heart. Several mutations of this gene have been identified and reported to be involved in several cardiac rhythm disorders, including type 3 l
Externí odkaz:
https://doaj.org/article/2250a954bf7944a28a19579b97aa2b90
Autor:
Zahia Touat-Hamici, Malorie Blancard, Ruifang Ma, Lianyun Lin, Yasmine Iddir, Isabelle Denjoy, Antoine Leenhardt, Zhiguang Yuchi, Pascale Guicheney
Publikováno v:
Scientific Reports, Vol 11, Iss 1, Pp 1-13 (2021)
Abstract Idiopathic ventricular fibrillation (IVF) causes sudden death in young adult patients without structural or ischemic heart disease. Most IVF cases are sporadic and some patients present with short-coupled torsade de pointes, the genetics of
Externí odkaz:
https://doaj.org/article/09050635e6e84eea9fe02cd858901af7
Autor:
Geraldine Landon, Isabelle Denjoy, Enora Clero, Aleksandr Silenok, Irina Kurnosova, Andrey Butsenin, Patrick Gourmelon, Jean-Rene Jourdain
Publikováno v:
Scientific Reports, Vol 11, Iss 1, Pp 1-9 (2021)
Abstract Between 2009 and 2013, a large cross-sectional study on the health consequences of the Chernobyl nuclear accident was performed in the contaminated and uncontaminated territories of the Bryansk Oblast (Russian Federation). The objective of t
Externí odkaz:
https://doaj.org/article/71712e424848443cb4e4b653e6bdb56c
Autor:
Barbara Oliveira‐Mendes, Sylvain Feliciangeli, Mélissa Ménard, Frank Chatelain, Malak Alameh, Jérôme Montnach, Sébastien Nicolas, Béatrice Ollivier, Julien Barc, Isabelle Baró, Jean‐Jacques Schott, Vincent Probst, Florence Kyndt, Isabelle Denjoy, Florian Lesage, Gildas Loussouarn, Michel De Waard
Publikováno v:
Clinical and Translational Medicine, Vol 11, Iss 11, Pp n/a-n/a (2021)
Abstract Background and aims Mutations in KCNH2 cause long or short QT syndromes (LQTS or SQTS) predisposing to life‐threatening arrhythmias. Over 1000 hERG variants have been described by clinicians, but most remain to be characterised. The object
Externí odkaz:
https://doaj.org/article/acbf1713166b446c8093329363ed25ac
Autor:
Plamen Bokov, Houmam El Jurdi, Isabelle Denjoy, Claudine Peiffer, Noria Medjahdi, Laurent Holvoet, Malika Benkerrou, Christophe Delclaux
Publikováno v:
Frontiers in Physiology, Vol 11 (2020)
BackgroundSickle cell disease (SCD) patients with asthma have an increased rate of vaso-occlusive crisis (VOC) and acute chest syndrome (ACS) episodes when compared to those without asthma. We hypothesized that either asthma diagnosis or bronchodilat
Externí odkaz:
https://doaj.org/article/3c9368948a104d8b965843a099bbec6c
Autor:
Anat Milman, Avi Sabbag, Giulio Conte, Pieter G. Postema, Antoine Andorin, Jean-Baptiste Gourraud, Frederic Sacher, Philippe Mabo, Sung-Hwan Kim, Shingo Maeda, Yoshihide Takahashi, Tsukasa Kamakura, Takeshi Aiba, Jimmy JM Juang, Yoav Michowitz, Eran Leshem, Yuka Mizusawa, Elena Arbelo, Zhengrong Huang, Isabelle Denjoy, Carla Giustetto, Yanushi D. Wijeyeratne, Andrea Mazzanti, Ramon Brugada, Ruben Casado-Arroyo, Jean Champagne, Leonardo Calo, Georgia Sarquella-Brugada, Jacob Tfelt-Hansen, Silvia G. Priori, Masahiko Takagi, Christian Veltmann, Pietro Delise, Domenico Corrado, Elijah R. Behr, Fiorenzo Gaita, Gan-Xin Yan, Josep Brugada, Antoine Leenhardt, Arthur A.M. Wilde, Pedro Brugada, Kengo F. Kusano, Kenzo Hirao, Gi-Byoung Nam, Vincent Probst, Bernard Belhassen
Publikováno v:
Circulation. Arrhythmia and electrophysiology, 16(1). Lippincott Williams and Wilkins
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fd94f987403608ac96a988912ee3b68e
https://pubmed.ncbi.nlm.nih.gov/36595628
https://pubmed.ncbi.nlm.nih.gov/36595628
Autor:
Carla Spazzolini, Isabelle Denjoy, Roel L.H.M.G. Spätjens, Peter J. Schwartz, Maria Christina Kotta, Paul A. Brink, Cristina Moreno, Kristina H. Haugaa, Sandrine R.M. Seyen, Maria Shkolnikova, Federica Dagradi, Lia Crotti, Marshall Heradien, Paul G.A. Volders, Silvia Castelletti, Matteo Pedrazzini
Publikováno v:
Eur Heart J
European Heart Journal, 42(46), 4743-4755. Oxford University Press
European Heart Journal, 42(46), 4743-4755. Oxford University Press
Aims Mutation type, location, dominant-negative I Ks reduction, and possibly loss of cyclic adenosine monophosphate (cAMP)-dependent I Ks stimulation via protein kinase A (PKA) influence the clinical severity of long QT syndrome type 1 (LQT1). Given
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::844d33f416c443ba9630554a3eb61ac2
https://doi.org/10.1093/eurheartj/ehab582
https://doi.org/10.1093/eurheartj/ehab582
Autor:
Antoine Leenhardt, Pierre Maison-Blanche, Isabelle Denjoy, Fabio Badilini, Pierre-Léo Laporte, Fabrice Extramiana, Martino Vaglio
Publikováno v:
Journal of Electrocardiology. 69:61-66
Background Brugada syndrome is a rare inherited arrhythmic syndrome with a coved type 1 ST-segment elevation on ECG and an increased risk of sudden death. Many studies have evaluated risk stratification performance based on ECG-derived parameters. Ho
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f294dd2d1ac46cf69d04e5e1ca8bfd14
https://doi.org/10.1016/j.jelectrocard.2021.09.009
https://doi.org/10.1016/j.jelectrocard.2021.09.009