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Vincent Portero

Showing results (11-20 of 18) with videos related to

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Journal of Internal Medicine|June 21, 2023
Light transmittance in human atrial tissue and transthoracic illumination in rats support translatability of optogenetic cardioversion of atrial fibrillationEmile C A Nyns, Vincent Portero, Shanliang Deng, et al.
Cardiovascular Research|September 16, 2021
Optical ventricular cardioversion by local optogenetic targeting and LED implantation in a cardiomyopathic rat modelEmile C A Nyns, Tianyi Jin, Magda S Fontes, et al.
Journal of the American Heart Association|June 12, 2016
Dysfunction of the Voltage-Gated K+ Channel β2 Subunit in a Familial Case of Brugada SyndromeVincent Portero, Solena Le Scouarnec, Zeineb Es-Salah-Lamoureux, et al.
Cardiovascular Research|June 18, 2021
Chronically elevated branched chain amino acid levels are pro-arrhythmicVincent Portero, Thomas Nicol, Svitlana Podliesna, et al.
Human Molecular Genetics|February 5, 2015
Testing the burden of rare variation in arrhythmia-susceptibility genes provides new insights into molecular diagnosis for Brugada syndromeSolena Le Scouarnec, Matilde Karakachoff, Jean-Baptiste Gourraud, et al.
Circulation Research|June 7, 2021
Targeting the Microtubule EB1-CLASP2 Complex Modulates Na<sub>V</sub>1.5 at Intercalated DiscsGerard A Marchal, Mariam Jouni, David Y Chiang, et al.
European Heart Journal|May 23, 2019
RRAD mutation causes electrical and cytoskeletal defects in cardiomyocytes derived from a familial case of Brugada syndromeNadjet Belbachir, Vincent Portero, Zeina R Al Sayed, et al.
Nature Genetics|July 23, 2013
Common variants at SCN5A-SCN10A and HEY2 are associated with Brugada syndrome, a rare disease with high risk of sudden cardiac deathConnie R Bezzina, Julien Barc, Yuka Mizusawa, et al.
Pageof 2

Showing results (11-20 of 18) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 18 results.
Journal of Internal Medicine|June 21, 2023
Light transmittance in human atrial tissue and transthoracic illumination in rats support translatability of optogenetic cardioversion of atrial fibrillationEmile C A Nyns, Vincent Portero, Shanliang Deng, et al.
Cardiovascular Research|September 16, 2021
Optical ventricular cardioversion by local optogenetic targeting and LED implantation in a cardiomyopathic rat modelEmile C A Nyns, Tianyi Jin, Magda S Fontes, et al.
Journal of the American Heart Association|June 12, 2016
Dysfunction of the Voltage-Gated K+ Channel β2 Subunit in a Familial Case of Brugada SyndromeVincent Portero, Solena Le Scouarnec, Zeineb Es-Salah-Lamoureux, et al.
Cardiovascular Research|June 18, 2021
Chronically elevated branched chain amino acid levels are pro-arrhythmicVincent Portero, Thomas Nicol, Svitlana Podliesna, et al.
Human Molecular Genetics|February 5, 2015
Testing the burden of rare variation in arrhythmia-susceptibility genes provides new insights into molecular diagnosis for Brugada syndromeSolena Le Scouarnec, Matilde Karakachoff, Jean-Baptiste Gourraud, et al.
Circulation Research|June 7, 2021
Targeting the Microtubule EB1-CLASP2 Complex Modulates Na<sub>V</sub>1.5 at Intercalated DiscsGerard A Marchal, Mariam Jouni, David Y Chiang, et al.
European Heart Journal|May 23, 2019
RRAD mutation causes electrical and cytoskeletal defects in cardiomyocytes derived from a familial case of Brugada syndromeNadjet Belbachir, Vincent Portero, Zeina R Al Sayed, et al.
Nature Genetics|July 23, 2013
Common variants at SCN5A-SCN10A and HEY2 are associated with Brugada syndrome, a rare disease with high risk of sudden cardiac deathConnie R Bezzina, Julien Barc, Yuka Mizusawa, et al.
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