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Prognostic value of ventricular arrhythmia in early post-infarction left ventricular dysfunction: the French nationwide WICD-MI study.
Published in:
European Heart Journal, 2024, v. 45, n. 41, p. 4428, doi. 10.1093/eurheartj/ehae575
By:
- Echivard, Mathieu;
- Sellal, Jean-Marc;
- Ziliox, Chloé;
- Marijon, Eloi;
- Bordachar, Pierre;
- Ploux, Sylvain;
- Benali, Karim;
- Marquié, Christelle;
- Docq, Clémence;
- Klug, Didier;
- Eschalier, Romain;
- Maille, Baptiste;
- Deharo, Jean-Claude;
- Babuty, Dominique;
- Genet, Thibaud;
- Gandjbakhch, Estelle;
- Costa, Antoine Da;
- Piot, Olivier;
- Minois, Damien;
- Gourraud, Jean-Baptiste
Publication type:
Article
Does sports participation increase risk in patients with long QT syndrome? Results from a large French cohort.
Published in:
2022
By:
- Davydoff, Caroline;
- Andorin, Antoine;
- Minois, Damien;
- Arnaud, Marine;
- Minier, Mathilde;
- Sacher, Frédéric;
- Martins, Raphael;
- Clementy, Nicolas;
- Gourraud, Jean Baptiste;
- Probst, Vincent
Publication type:
journal article
Time-to-first appropriate shock in patients implanted prophylactically with an implantable cardioverter-defibrillator: data from the Survey on Arrhythmic Events in BRUgada Syndrome (SABRUS).
Published in:
2019
By:
- Milman, Anat;
- Hochstadt, Aviram;
- Andorin, Antoine;
- Gourraud, Jean-Baptiste;
- Sacher, Frederic;
- Mabo, Philippe;
- Kim, Sung-Hwan;
- Conte, Giulio;
- Arbelo, Elena;
- Kamakura, Tsukasa;
- Aiba, Takeshi;
- Napolitano, Carlo;
- Giustetto, Carla;
- Denjoy, Isabelle;
- Juang, Jimmy J M;
- Maeda, Shingo;
- Takahashi, Yoshihide;
- Leshem, Eran;
- Michowitz, Yoav;
- Rahkovich, Michael
Publication type:
journal article
Mental stress test: a rapid, simple, and efficient test to unmask long QT syndrome.
Published in:
2018
By:
- Etienne, Pauline;
- Huchet, François;
- Gaborit, Nathalie;
- Barc, Julien;
- Thollet, Aurélie;
- Kyndt, Florence;
- Guyomarch, Béatrice;
- Marec, Hervé Le;
- Charpentier, Flavien;
- Schott, Jean-Jacques;
- Le Marec, Hervé;
- Redon, Richard;
- Probst, Vincent;
- Gourraud, Jean-Baptiste
Publication type:
journal article
Correlation of intracardiac electrogram with surface electrocardiogram in Brugada syndrome patients.
Published in:
2014
By:
- Probst, Vincent;
- Sacher, Frederic;
- Derval, Nicolas;
- Gourraud, Jean Baptiste;
- Mabo, Philippe;
- Medkour, Fariza;
- Marec, Hervé Le;
- Gill, John
Publication type:
Journal Article
Correlation of intracardiac electrogram with surface electrocardiogram in Brugada syndrome patients.
Published in:
EP: Europace, 2014, v. 16, n. 6, p. 908, doi. 10.1093/europace/eut294
By:
- Probst, Vincent;
- Sacher, Frederic;
- Derval, Nicolas;
- Gourraud, Jean Baptiste;
- Mabo, Philippe;
- Medkour, Fariza;
- Marec, Hervé Le;
- Gill, John
Publication type:
Article
Incomplete Timothy syndrome secondary to a mosaic mutation of the CACNA1C gene diagnosed using next-generation sequencing.
Published in:
American Journal of Medical Genetics. Part A, 2017, v. 173, n. 2, p. 531, doi. 10.1002/ajmg.a.38045
By:
- Baurand, Amandine;
- Falcon‐Eicher, Sylvie;
- Laurent, Gabriel;
- Villain, Elisabeth;
- Bonnet, Caroline;
- Thauvin‐Robinet, Christel;
- Jacquot, Caroline;
- Eicher, Jean‐Christophe;
- Gourraud, Jean‐Baptiste;
- Schmitt, Sébastien;
- Bézieau, Stéphane;
- Giraud, Mathilde;
- Dumont, Solenne;
- Kuentz, Paul;
- Probst, Vincent;
- Burguet, Antoine;
- Kyndt, Florence;
- Faivre, Laurence
Publication type:
Article
Common variants at SCN5A-SCN10A and HEY2 are associated with Brugada syndrome, a rare disease with high risk of sudden cardiac death.
Published in:
Nature Genetics, 2013, v. 45, n. 11, p. 1409, doi. 10.1038/ng1113-1409b
By:
- Bezzina, Connie R;
- Barc, Julien;
- Mizusawa, Yuka;
- Remme, Carol Ann;
- Gourraud, Jean-Baptiste;
- Simonet, Floriane;
- Verkerk, Arie O;
- Schwartz, Peter J;
- Crotti, Lia;
- Dagradi, Federica;
- Guicheney, Pascale;
- Fressart, Véronique;
- Leenhardt, Antoine;
- Antzelevitch, Charles;
- Bartkowiak, Susan;
- Schulze-Bahr, Eric;
- Zumhagen, Sven;
- Behr, Elijah R;
- Bastiaenen, Rachel;
- Tfelt-Hansen, Jacob
Publication type:
Article
Common variants at SCN5A-SCN10A and HEY2 are associated with Brugada syndrome, a rare disease with high risk of sudden cardiac death.
Published in:
Nature Genetics, 2013, v. 45, n. 9, p. 1044, doi. 10.1038/ng.2712
By:
- Bezzina, Connie R;
- Barc, Julien;
- Mizusawa, Yuka;
- Remme, Carol Ann;
- Gourraud, Jean-Baptiste;
- Simonet, Floriane;
- Verkerk, Arie O;
- Schwartz, Peter J;
- Crotti, Lia;
- Dagradi, Federica;
- Guicheney, Pascale;
- Fressart, Véronique;
- Leenhardt, Antoine;
- Antzelevitch, Charles;
- Bartkowiak, Susan;
- Schulze-Bahr, Eric;
- Zumhagen, Sven;
- Behr, Elijah R;
- Bastiaenen, Rachel;
- Tfelt-Hansen, Jacob
Publication type:
Article
Implantable cardioverter defibrillator use in arrhythmogenic right ventricular cardiomyopathy in North America and Europe.
Published in:
European Heart Journal, 2024, v. 45, n. 7, p. 538, doi. 10.1093/eurheartj/ehad799
By:
- Carrick, Richard T;
- Marco, Corrado De;
- Gasperetti, Alessio;
- Bosman, Laurens P;
- Gourraud, Jean-Baptiste;
- Trancuccio, Alessandro;
- Mazzanti, Andrea;
- Murray, Brittney;
- Pendleton, Catherine;
- Tichnell, Crystal;
- Tandri, Harikrishna;
- Zeppenfeld, Katja;
- Wilde, Arthur A M;
- Davies, Brianna;
- Seifer, Colette;
- Roberts, Jason D;
- Healey, Jeff S;
- MacIntyre, Ciorsti;
- Alqarawi, Wael;
- Tadros, Rafik
Publication type:
Article
Arrhythmic risk prediction in arrhythmogenic right ventricular cardiomyopathy: external validation of the arrhythmogenic right ventricular cardiomyopathy risk calculator.
Published in:
European Heart Journal, 2022, v. 43, n. 32, p. 3041, doi. 10.1093/eurheartj/ehac289
By:
- Jordà, Paloma;
- Bosman, Laurens P;
- Gasperetti, Alessio;
- Mazzanti, Andrea;
- Gourraud, Jean Baptiste;
- Davies, Brianna;
- Frederiksen, Tanja Charlotte;
- Weidmann, Zoraida Moreno;
- Marco, Andrea Di;
- Roberts, Jason D;
- MacIntyre, Ciorsti;
- Seifer, Colette;
- Delinière, Antoine;
- Alqarawi, Wael;
- Kukavica, Deni;
- Minois, Damien;
- Trancuccio, Alessandro;
- Arnaud, Marine;
- Targetti, Mattia;
- Martino, Annamaria
Publication type:
Article
RRAD mutation causes electrical and cytoskeletal defects in cardiomyocytes derived from a familial case of Brugada syndrome.
Published in:
European Heart Journal, 2019, v. 40, n. 37, p. 3081, doi. 10.1093/eurheartj/ehz308
By:
- Belbachir, Nadjet;
- Portero, Vincent;
- Sayed, Zeina R Al;
- Gourraud, Jean-Baptiste;
- Dilasser, Florian;
- Jesel, Laurence;
- Guo, Hongchao;
- Wu, Haodi;
- Gaborit, Nathalie;
- Guilluy, Christophe;
- Girardeau, Aurore;
- Bonnaud, Stephanie;
- Simonet, Floriane;
- Karakachoff, Matilde;
- Pattier, Sabine;
- Scott, Carol;
- Burel, Sophie;
- Marionneau, Céline;
- Chariau, Caroline;
- Gaignerie, Anne
Publication type:
Article
A consistent arrhythmogenic trait in Brugada syndrome cellular phenotype.
Published in:
Clinical & Translational Medicine, 2021, v. 11, n. 6, p. 1, doi. 10.1002/ctm2.413
By:
- Al Sayed, Zeina R.;
- Jouni, Mariam;
- Gourraud, Jean‐Baptiste;
- Belbachir, Nadjet;
- Barc, Julien;
- Girardeau, Aurore;
- Forest, Virginie;
- Derevier, Aude;
- Gaignerie, Anne;
- Chariau, Caroline;
- Cimarosti, Bastien;
- Canac, Robin;
- Olchesqui, Pierre;
- Charpentier, Eric;
- Schott, Jean‐Jacques;
- Redon, Richard;
- Baró, Isabelle;
- Probst, Vincent;
- Charpentier, Flavien;
- Loussouarn, Gildas
Publication type:
Article
Implantable cardiac defibrillator leads dysfunction after LVAD implantation.
Published in:
Pacing & Clinical Electrophysiology, 2020, v. 43, n. 11, p. 1309, doi. 10.1111/pace.14004
By:
- Galand, Vincent;
- Leclercq, Christophe;
- Bourenane, Hamed;
- Boulé, Stéphane;
- Vincentelli, André;
- Maury, Philippe;
- Mondoly, Pierre;
- Picard, François;
- Welté, Nicolas;
- Kindo, Michel;
- Cardi, Thomas;
- Pasquié, Jean‐Luc;
- Gaudard, Philippe;
- Gourraud, Jean‐Baptiste;
- Probst, Vincent;
- Defaye, Pascal;
- Boignard, Aude;
- Para, Marylou;
- Algalarrondo, Vincent;
- Pelcé, Edeline
Publication type:
Article
Human model of IRX5 mutations reveals key role for this transcription factor in ventricular conduction.
Published in:
Cardiovascular Research, 2021, v. 117, n. 9, p. 2092, doi. 10.1093/cvr/cvaa259
By:
- Sayed, Zeina R Al;
- Canac, Robin;
- Cimarosti, Bastien;
- Bonnard, Carine;
- Gourraud, Jean-Baptiste;
- Hamamy, Hanan;
- Kayserili, Hulya;
- Girardeau, Aurore;
- Jouni, Mariam;
- Jacob, Nicolas;
- Gaignerie, Anne;
- Chariau, Caroline;
- David, Laurent;
- Forest, Virginie;
- Marionneau, Céline;
- Charpentier, Flavien;
- Loussouarn, Gildas;
- Lamirault, Guillaume;
- Reversade, Bruno;
- Zibara, Kazem
Publication type:
Article
Dysfunction of the Voltage-Gated K+ Channel β2 Subunit in a Familial Case of Brugada Syndrome.
Published in:
2016
By:
- Portero, Vincent;
- Le Scouarnec, Solena;
- Es ‐ Salah ‐ Lamoureux, Zeineb;
- Burel, Sophie;
- Gourraud, Jean ‐ Baptiste;
- Bonnaud, Stéphanie;
- Lindenbaum, Pierre;
- Simonet, Floriane;
- Violleau, Jade;
- Baron, Estelle;
- Moreau, Eléonore;
- Scott, Carol;
- Chatel, Stéphanie;
- Loussouarn, Gildas;
- O'Hara, Thomas;
- Mabo, Philippe;
- Dina, Christian;
- Le Marec, Hervé;
- Schott, Jean ‐ Jacques;
- Probst, Vincent
Publication type:
journal article
Testing the burden of rare variation in arrhythmia-susceptibility genes provides new insights into molecular diagnosis for Brugada syndrome.
Published in:
Human Molecular Genetics, 2015, v. 24, n. 10, p. 2757, doi. 10.1093/hmg/ddv036
By:
- Le Scouarnec, Solena;
- Karakachoff, Matilde;
- Gourraud, Jean-Baptiste;
- Lindenbaum, Pierre;
- Bonnaud, Stéphanie;
- Portero, Vincent;
- Duboscq-Bidot, Laëtitia;
- Daumy, Xavier;
- Simonet, Floriane;
- Teusan, Raluca;
- Baron, Estelle;
- Violleau, Jade;
- Persyn, Elodie;
- Bellanger, Lise;
- Barc, Julien;
- Chatel, Stéphanie;
- Martins, Raphaël;
- Mabo, Philippe;
- Sacher, Frédéric;
- Haïssaguerre, Michel
Publication type:
Article
Incidence and predictors of sudden death, major conduction defects and sustained ventricular tachyarrhythmias in 1388 patients with myotonic dystrophy type 1.
Published in:
European Heart Journal, 2017, v. 38, n. 10, p. 751, doi. 10.1093/eurheartj/ehw569
By:
- Wahbi, Karim;
- Babuty, Dominique;
- Probst, Vincent;
- Wissocque, Ludivine;
- Labombarda, Fabien;
- Porcher, Raphaël;
- écane, Henri Marc B.;
- Lazarus, Arnaud;
- Béhin, Anthony;
- Laforêt, Pascal;
- Stojkovic, Tanya;
- Clementy, Nicolas;
- Dussauge, Aurélie Pattier;
- Gourraud, Jean Baptiste;
- Pereon, Yann;
- Lacour, Arnaud;
- Chapon, Françoise;
- Milliez, Paul;
- Klug, Didier;
- Eymard, Bruno
Publication type:
Article
Complex Brugada syndrome inheritance in a family harbouring compound SCN5A and CACNA1C mutations.
Published in:
Basic Research in Cardiology, 2014, v. 109, n. 6, p. 1, doi. 10.1007/s00395-014-0446-5
By:
- Béziau, Delphine M.;
- Barc, Julien;
- O’Hara, Thomas;
- Le Gloan, Laurianne;
- Amarouch, Mohamed Yassine;
- Solnon, Aude;
- Pavin, Dominique;
- Lecointe, Simon;
- Bouillet, Patricia;
- Gourraud, Jean-Baptiste;
- Guicheney, Pascale;
- Denjoy, Isabelle;
- Redon, Richard;
- Mabo, Philippe;
- le Marec, Hervé;
- Loussouarn, Gildas;
- Kyndt, Florence;
- Schott, Jean-Jacques;
- Probst, Vincent;
- Baró, Isabelle
Publication type:
Article

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