Systematic analysis of SCN5A variants associated with inherited cardiac diseases

Autor: Hermida, Alexis, Jedraszak, Guillaume, Ader, Flavie, Denjoy, Isabelle, Fressart, Véronique, Maury, Phillipe, Beyls, Christophe, Bloch, Adrien, Clerici, Gaël, Daire, Elise, Defaye, Pascal, Dupin-Deguine, Delphine, Garçon, Loic, Klug, Didier, Ginglinger, Emmanuelle, Hermida, Jean-Sylvain, Jesel, Laurence, Khraiche, Diala, Kubala, Maciej, Lacotte, Jérôme, Laredo, Mikael, Leenhardt, Antoine, Le Guillou, Xavier, Lesaffre, Francois, Maltret, Alice, Magnin-Poull, Isabelle, Marijon, Eloi, Nambot, Sophie, Neyroud, Nathalie, Ninni, Sandro, Palmyre, Aurélien, Pasquie, Jean Luc, Proukhnitzky, Julie, Reant, Patricia, Richard, Pascale, Rollin, Anne, Rooryck, Caroline, Sacher, Frédéric, Schaefer, Elise, Vernier, Agathe, Winum, Pierre-François, Wahbi, Karim, Waintraub, Xavier, Waldmann, Victor, Weber, Sacha, Zouaghi, Amir, Charron, Philippe, Extramiana, Fabrice, Gandjbakhch, Estelle

Publikováno v: In Heart Rhythm

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Editorial: Methods and applications in cardiac electrophysiology--application to inherited arrhythmias.

Autor: Neyroud, Nathalie, Baró, Isabelle, Maguy, Ange

Publikováno v: Frontiers in Physiology; 2024, p1-3, 3p

Characterization of Purkinje-like cardiac cells derived from iPS cells from patients with Purkinje-induced idiopathic ventricular fibrillation

Autor: Belhumeur, Pauline, Fontaine, Vincent, Surget, Elodie, Bernus, Olivier, Extramiana, Fabrice, Haissaguerre, Michel, Gandjbakhch, Estelle, Neyroud, Nathalie

Publikováno v: In Archives of Cardiovascular Diseases June-July 2024 117(6-7) Supplement:S208-S208

A Type 2 Ryanodine Receptor Variant in the Helical Domain 2 Associated with an Impairment of the Adrenergic Response

Autor: Blancard, Malorie, Touat-Hamici, Zahia, Aguilar-Sanchez, Yuriana, Yin, Liheng, Vaksmann, Guy, Roux-Buisson, Nathalie, Fressart, Véronique, Denjoy, Isabelle, Klug, Didier, Neyroud, Nathalie, Ramos-Franco, Josefina, Gomez, Ana Maria, Guicheney, Pascale

Publikováno v: Journal of Personalized Medicine
Journal of Personalized Medicine, 2021, 11 (6), pp.579. ⟨10.3390/jpm11060579⟩
Journal of Personalized Medicine, MDPI, 2021, 11 (6), pp.579. ⟨10.3390/jpm11060579⟩
Volume 11
Issue 6
Journal of Personalized Medicine, Vol 11, Iss 579, p 579 (2021)

Catecholaminergic polymorphic ventricular tachycardia (CPVT) is triggered by exercise or acute emotion in patients with normal resting electrocardiogram. The major disease-causing gene is RYR2, encoding the cardiac ryanodine receptor (RyR2). We repor

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::3b4d40ea143263198fb944a0eca493d2
https://hal.sorbonne-universite.fr/hal-03278104