Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Jean‐Baptiste Reisqs"'
Autor:
Yvonne Sleiman, Jean-Baptiste Reisqs, Reina Bianca Tan, Frank Cecchin, Mohamed Chahine, Mohamed Boutjdir
Publikováno v:
Stem Cell Research, Vol 81, Iss , Pp 103608- (2024)
Progressive cardiac conduction defect often associated with variants in sodium voltage-gated channel SCN5A gene and variants in the L-type calcium voltage-gated channel CACNA1D gene are implicated in sinoatrial node dysfunction. We generated an induc
Externí odkaz:
https://doaj.org/article/2f16ff1b252244dbbb220f32bfc809b1
Publikováno v:
Frontiers in Cardiovascular Medicine, Vol 11 (2024)
Heart failure (HF) is recognized as an epidemic in the contemporary world, impacting around 1%–2% of the adult population and affecting around 6 million Americans. HF remains a major cause of mortality, morbidity, and poor quality of life. Several
Externí odkaz:
https://doaj.org/article/d35ebb4cc31246ff8cbe1900a92b88be
Autor:
Vamsi Krishna Murthy Ginjupalli, Michael Cupelli, Jean-Baptiste Reisqs, Yvonne Sleiman, Nabil El-Sherif, Genevieve Gourdon, Jack Puymirat, Mohamed Chahine, Mohamed Boutjdir
Publikováno v:
Frontiers in Physiology, Vol 14 (2023)
Introduction: Myotonic dystrophy type 1 (DM1) is a multisystemic genetic disorder caused by the increased number of CTG repeats in 3′ UTR of Dystrophia Myotonia Protein Kinase (DMPK) gene. DM1 patients experience conduction abnormalities as well as
Externí odkaz:
https://doaj.org/article/0e83e010915a4304aa31e83301e517c2
Autor:
Jean‐Baptiste Reisqs, Adrien Moreau, Azzouz Charrabi, Yvonne Sleiman, Albano C. Meli, Gilles Millat, Veronique Briand, Philippe Beauverger, Sylvain Richard, Philippe Chevalier
Publikováno v:
Clinical and Translational Medicine, Vol 12, Iss 3, Pp n/a-n/a (2022)
Externí odkaz:
https://doaj.org/article/174def93689b448da721e6a61e866ef2
Autor:
Adrien Moreau, Jean‐Baptiste Reisqs, Helene Delanoe‐Ayari, Marion Pierre, Alexandre Janin, Antoine Deliniere, Francis Bessière, Albano C. Meli, Azzouz Charrabi, Estele Lafont, Camille Valla, Delphine Bauer, Elodie Morel, Vincent Gache, Gilles Millat, Xavier Nissan, Adele Faucherre, Chris Jopling, Sylvain Richard, Alexandre Mejat, Philippe Chevalier
Publikováno v:
Clinical and Translational Medicine, Vol 11, Iss 3, Pp n/a-n/a (2021)
Abstract Background Severe ventricular rhythm disturbances are the hallmark of arrhythmogenic cardiomyopathy (ACM), and are often explained by structural conduction abnormalities. However, comprehensive investigations of ACM cell electrical instabili
Externí odkaz:
https://doaj.org/article/c9664adcb3fe4088aa3cbb1ca8360b5b
Autor:
Jean‐Baptiste Reisqs, Adrien Moreau, Azzouz Charrabi, Yvonne Sleiman, Albano C. Meli, Gilles Millat, Veronique Briand, Philippe Beauverger, Sylvain Richard, Philippe Chevalier
Publikováno v:
Clinical and Translational Medicine
Clinical and Translational Medicine, 2022, 12 (3), ⟨10.1002/ctm2.748⟩
Clinical and Translational Medicine, 2022, 12 (3), ⟨10.1002/ctm2.748⟩
International audience; No abstract available
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::125c22bd6923b66b70a8ae7507898904
https://pubmed.ncbi.nlm.nih.gov/35297182
https://pubmed.ncbi.nlm.nih.gov/35297182