QT length during methadone maintenance treatment: gene × dose interaction

Autor: Frank Bellivier, François Naccache, Vanessa Bloch, Jean Pierre Lepine, Florence Vorspan, Stéphane Mouly, Andries T. Marees, Cynthia Marie-Claire, Nathalie Prince, Jean-Louis Laplanche, El Hadi Zerdazi

Publikováno v: Fundamental and Clinical Pharmacology
Fundamental and Clinical Pharmacology, Wiley, 2018, ⟨10.1111/fcp.12405⟩
Fundamental and Clinical Pharmacology, 33(1), 96-106. Wiley-Blackwell
Fundamental and Clinical Pharmacology, Wiley, 2019, 33 (1), pp.96-106. ⟨10.1111/fcp.12405⟩
Zerdazi, E H, Vorspan, F, Marees, A T, Naccache, F, Lepine, J P, Laplanche, J L, Prince, N, Marie-Claire, C, Bellivier, F, Mouly, S & Bloch, V 2019, ' QT length during methadone maintenance treatment: gene × dose interaction ', Fundamental and Clinical Pharmacology, vol. 33, no. 1, pp. 96-106 . https://doi.org/10.1111/fcp.12405
Fundamental & clinical pharmacology, 33(1), 96-106. Wiley-Blackwell
Fundamental & Clinical Pharmacology
Fundamental & Clinical Pharmacology, 2018, 33 (1), pp.96-106. ⟨10.1111/fcp.12405⟩

Methadone is known to be a risk factor for sudden death by enlarging ECG QT corrected (QTc) interval. For other medical conditions, QTc lengthening has been described as the result of interactions between pharmacological treatments and genetic factor

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::eedcda2f7771c5a7b3a9a973b2b0e12c
https://doi.org/10.1111/fcp.12405

Effects of peripherally administered urotensin II and arginine vasotocin on the QT interval of the electrocardiogram in trout

Autor: Jean-Claude Le Mével, Jérôme Leprince, Hubert Vaudry, Frédéric Lancien, Gilmer Vanegas

Publikováno v: Comparative Biochemistry and Physiology-Part C: Toxicology and Pharmacology
Comparative Biochemistry and Physiology-Part C: Toxicology and Pharmacology, Elsevier, 2016, 183-184, pp.53-60. ⟨10.1016/j.cbpc.2016.01.006⟩

International audience; The QT interval of the electrocardiogram (ECG) is a measure of the duration of the ventricular depolarization and repolarization. In fish as in human, the QT interval is positively correlated with the RR interval of the ECG, a

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5d6519183e5c43be4777429540472cef
https://pubmed.ncbi.nlm.nih.gov/26902806

Different circadian behavior of the apex and the end of the T wave

Autor: N. Neyroud, Jocelyne Fayn, D. Catuli, Philippe Coumel, Paul Rubel, P. Maison-Blanche

Publikováno v: Journal of Electrocardiology
Journal of Electrocardiology, Elsevier, 1995, 28, pp.138-142. ⟨10.1016/s0022-0736(95)80039-5⟩

International audience

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c0f93b0b933d3fe973af941ddab2bfbc
https://doi.org/10.1016/s0022-0736(95)80039-5

Characterization of novel KCNH2 mutations in type 2 long QT syndrome manifesting as seizures.: Characterizing novel KCNH2 mutations

Autor: Keller, Dagmar, Grenier, Julie, Christé, Georges, Dubouloz, Frédérique, Osswald, Stephan, Brink, Marijke, Ficker, Eckhard, Chahine, Mohamed

Publikováno v: Canadian Journal of Cardiology
Canadian Journal of Cardiology, Elsevier, 2009, 25 (8), pp.455-62

International audience; BACKGROUND: Long QT syndrome (LQTS) is characterized by corrected QT interval prolongation leading to torsades de pointes and sudden cardiac death. LQTS type 2 (LQTS2) is caused by mutations in the KCNH2 gene, leading to a red

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=od_______212::d5bbc6cd72c5503f3c1b252050476c2f
https://www.hal.inserm.fr/inserm-00409709/file/Keller-D_2009_Can_J_Cardiol.pdf

Role of congenital long-QT syndrome in unexplained sudden infant death: proposal for an electrocardiographic screening in relatives

Autor: Frédéric Treguer, Remi Baruteau, Raphaël P. Martins, Philippe Mabo, Alban-Elouen Baruteau, Ryad Joomye, Jean-Claude Daubert, Julien Baruteau, Michel Roussey

Publikováno v: European Journal of Pediatrics
European Journal of Pediatrics, Springer Verlag, 2009, 168 (7), pp.771-7. ⟨10.1007/s00431-009-0951-y⟩
European Journal of Pediatrics, 2009, 168 (7), pp.771-7. ⟨10.1007/s00431-009-0951-y⟩

International audience; INTRODUCTION: Congenital long-QT syndrome (LQTS) is a sporadic or familial inherited arrhythmia. It can lead to sudden death by ventricular fibrillation which occurs at any age but particularly during infancy. Recent studies o

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c85170520ca0f4131b0dff28c6b4cda0
https://hal.archives-ouvertes.fr/hal-00911293