Результати пошуку - Florence Kyndt

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  1. 1
    Haploinsufficiency in combination with aging causes SCN5A-linked hereditary Lenègre disease

    Haploinsufficiency in combination with aging causes SCN5A-linked hereditary Lenègre disease за авторством Vincent Probst, Florence Kyndt, F Potet, Jean‐Noël Trochu, G Mialet, Sophie Demolombe, Jean‐Jacques Schott, Isabelle Baró, Denis Escande, Hervé Le Marec

    Опубліковано 2003
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  2. 2
    Response to intravenous ajmaline: a retrospective analysis of 677 ajmaline challenges

    Response to intravenous ajmaline: a retrospective analysis of 677 ajmaline challenges за авторством Christian Veltmann, C. Wolpert, Frédéric Sacher, Philippe Mabo, Rainer Schimpf, Florian Streitner, Joachim Brade, Florence Kyndt, Juergen Kuschyk, H. Le Marec, M. Borggrefe, Vincent Probst

    Опубліковано 2009
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  3. 3
    0268 : Involvement of LRRFip1 gene and canonical Wnt pathway in Mitral Valve Prolapse (MVP)

    0268 : Involvement of LRRFip1 gene and canonical Wnt pathway in Mitral Valve Prolapse (MVP) за авторством Pauline Labbé, Emilie Faure, Simon Lecointe, Florence Kyndt, Thierry Le Tourneau, José Luís de la Pompa, Cécile Duplàa, Stéphane Zaffran, Jean‐Jacques Schott, Jean Mérot

    Опубліковано 2015
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  4. 4
    Novel <i>SCN5A</i> Mutation Leading Either to Isolated Cardiac Conduction Defect or Brugada Syndrome in a Large French Family

    Novel <i>SCN5A</i> Mutation Leading Either to Isolated Cardiac Conduction Defect or Brugada Syndrome in a Large French Family за авторством Florence Kyndt, Vincent Probst, F Potet, Sophie Demolombe, Jean-Christophe Chevallier, Isabelle Baró, Jean-Paul Moisan, Pierre Boisseau, Jean‐Jacques Schott, Denis Escande, Hervé Le Marec

    Опубліковано 2001
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  5. 5
    Screening for Copy Number Variation in Genes Associated With the Long QT Syndrome

    Screening for Copy Number Variation in Genes Associated With the Long QT Syndrome за авторством Julien Barc, François Briec, Sébastien Schmitt, Florence Kyndt, Martine Le Cunff, Estelle Baron, C Vieyres, Frédéric Sacher, Richard Redon, Cédric Le Caignec, Hervé Le Marec, Vincent Probst, Jean‐Jacques Schott

    Опубліковано 2010
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  6. 6
    Mapping of X-Linked Myxomatous Valvular Dystrophy to Chromosome Xq28

    Mapping of X-Linked Myxomatous Valvular Dystrophy to Chromosome Xq28 за авторством Florence Kyndt, Jean‐Jacques Schott, Jean‐Noël Trochu, Florence Baranger, O. Herbert, Valerie E. Scott, Édith Fressinaud, Albert David, Jean‐Paul Moisan, Jean-Brieuc Bouhour, Hervé Le Marec, Bernard Bénichou

    Опубліковано 1998
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  7. 7
    Familial screening in case of acute myocarditis reveals inherited arrhythmogenic left ventricular cardiomyopathies

    Familial screening in case of acute myocarditis reveals inherited arrhythmogenic left ventricular cardiomyopathies за авторством Nicolas Piriou, Lara Marteau, Florence Kyndt, Jean Michel Serfaty, Claire Toquet, Laurianne Le Gloan, K. Warin-Fresse, Damien Guijarro, Thierry Le Tourneau, E Conan, Aurélie Thollet, Vincent Probst, Jean‐Noël Trochu

    Опубліковано 2020
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  8. 8
    Cardiac characteristics and long-term outcome in Andersen-Tawil syndrome patients related to KCNJ2 mutation

    Cardiac characteristics and long-term outcome in Andersen-Tawil syndrome patients related to KCNJ2 mutation за авторством E Delannoy, F. Sacher, Philippe Maury, Philippe Mabo, Jacques Mansourati, Isabelle E. Magnin, Jean-Pierre Camous, G. Tournant, Elisabeth Sornay‐Rendu, Florence Kyndt, M. Haïssaguerre, Stéphane Bézieau, Béatrice Guyomarch, Hervé Le Marec, Véronique Fressart, Isabelle Denjoy, Vincent Probst

    Опубліковано 2013
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  9. 9
    Age at diagnosis of Brugada syndrome: Influence on clinical characteristics and risk of arrhythmia

    Age at diagnosis of Brugada syndrome: Influence on clinical characteristics and risk of arrhythmia за авторством Mathilde Minier, Vincent Probst, P. Berthome, Romain Tixier, Jean Paul Briand, Olivier Geoffroy, Nicolas Clémenty, Jacques Mansourati, Laurence Jesel, Jean‐Marc Dupuis, Paul Bru, Florence Kyndt, Béatrice Guyomarch, Aurélie Thollet, Nathalie Béhar, Philippe Mabo, Frédéric Sacher, Jean‐Baptiste Gourraud

    Опубліковано 2019
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  10. 10
    Mutations in the Gene Encoding Filamin A as a Cause for Familial Cardiac Valvular Dystrophy

    Mutations in the Gene Encoding Filamin A as a Cause for Familial Cardiac Valvular Dystrophy за авторством Florence Kyndt, Jean-Pierre Gueffet, Vincent Probst, Philippe Jaafar, Antoine Legendre, Françoise Le Bouffant, Claire Toquet, Estelle Roy, Lesley McGregor, Sally Ann Lynch, Ruth Newbury-Ecob, Vinh Tran, Ian Young, Jean‐Noël Trochu, Hervé Le Marec, Jean‐Jacques Schott

    Опубліковано 2006
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  11. 11
    SCN5A Mutations and the Role of Genetic Background in the Pathophysiology of Brugada Syndrome

    SCN5A Mutations and the Role of Genetic Background in the Pathophysiology of Brugada Syndrome за авторством Vincent Probst, Arthur A.M. Wilde, Julien Barc, Frédéric Sacher, Dominique Babuty, Philippe Mabo, Jacques Mansourati, Solena Le Scouarnec, Florence Kyndt, Cédric Le Caignec, Pascale Guicheney, Laëtitia Gouas, Juliette Albuisson, Paola G. Meregalli, Hervé Le Marec, Hanno L. Tan, Jean‐Jacques Schott

    Опубліковано 2009
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  12. 12
    Sodium-channel blocker challenge in the familial screening of Brugada syndrome: Safety and predictors of positivity

    Sodium-channel blocker challenge in the familial screening of Brugada syndrome: Safety and predictors of positivity за авторством Dylan Therasse, Frédéric Sacher, Bertrand Petit, Dominique Babuty, Philippe Mabo, Raphaël P. Martins, Laurence Jesel, Philippe Maury, Jean‐Luc Pasquié, Jacques Mansourati, J. Dupuis, Florence Kyndt, Aurélie Thollet, Béatrice Guyomarch, Julien Barc, Jean‐Jacques Schott, Hervé Le Marec, Richard Redon, Vincent Probst, Jean‐Baptiste Gourraud

    Опубліковано 2017
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  13. 13
    Targeted resequencing identifies TRPM4 as a major gene predisposing to progressive familial heart block type I

    Targeted resequencing identifies TRPM4 as a major gene predisposing to progressive familial heart block type I за авторством Xavier Daumy, Mohamed‐Yassine Amarouch, Pierre Lindenbaum, Stéphanie Bonnaud, Éric Charpentier, Beatrice Bianchi, Sabine Nafzger, Estelle Baron, Swanny Fouchard, Aurélie Thollet, Florence Kyndt, Julien Barc, Solena Le Scouarnec, Naomasa Makita, Hervé Le Marec, Christian Dina, Jean‐Baptiste Gourraud, Vincent Probst, Hugues Abriel, Richard Redon, Jean‐Jacques Schott

    Опубліковано 2016
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  14. 14
    Absence of triadin, a protein of the calcium release complex, is responsible for cardiac arrhythmia with sudden death in human

    Absence of triadin, a protein of the calcium release complex, is responsible for cardiac arrhythmia with sudden death in human за авторством Nathalie Roux-Buisson, Marine Cacheux, Anne Fourest‐Lieuvin, Jérémy Fauconnier, Julie Brocard, Isabelle Denjoy, Philippe Durand, Pascale Guicheney, Florence Kyndt, Antoine Leenhardt, Hervé Le Marec, V. Lucet, Philippe Mabo, Vincent Probst, Nicole Monnier, Pierre F. Ray, Elodie Santoni, Pauline Trémeaux, Alain Lacampagne, Julien Fauré, Joël Lunardi, Isabelle Marty

    Опубліковано 2012
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  15. 15
    Multifocal Ectopic Purkinje-Related Premature Contractions

    Multifocal Ectopic Purkinje-Related Premature Contractions за авторством Gabriel Laurent, Samuel Saal, Mohamed‐Yassine Amarouch, Delphine Béziau, Roos F. Marsman, Laurence Faivre, Julien Barc, Christian Dina, Géraldine Bertaux, Olivier Barthez, Christel Thauvin‐Robinet, Philippe Charron, Véronique Fressart, Alice Maltret, E Villain, Estelle Baron, Jean Mérot, Rodolphe Turpault, Yves Coudière, Flavien Charpentier, Jean‐Jacques Schott, Gildas Loussouarn, Arthur A.M. Wilde, Jean‐Eric Wolf, Isabelle Baró, Florence Kyndt, Vincent Probst

    Опубліковано 2012
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  16. 16
    Testing the burden of rare variation in arrhythmia-susceptibility genes provides new insights into molecular diagnosis for Brugada syndrome

    Testing the burden of rare variation in arrhythmia-susceptibility genes provides new insights into molecular diagnosis for Brugada syndrome за авторством Solena Le Scouarnec, Matilde Karakachoff, Jean‐Baptiste Gourraud, Pierre Lindenbaum, Stéphanie Bonnaud, Vincent Portero, Laëtitia Duboscq-Bidot, Xavier Daumy, Floriane Simonet, Raluca Teusan, Estelle Baron, Jade Violleau, Elodie Persyn, Lise Bellanger, Julien Barc, Stéphanie Chatel, Raphaël P. Martins, Philippe Mabo, Frédéric Sacher, Michel Haı̈ssaguerre, Florence Kyndt, Sébastien Schmitt, Stéphane Bézieau, Hervé Le Marec, Christian Dina, Jean‐Jacques Schott, Vincent Probst, Richard Redon

    Опубліковано 2015
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  17. 17
    An international compendium of mutations in the SCN5A-encoded cardiac sodium channel in patients referred for Brugada syndrome genetic testing

    An international compendium of mutations in the SCN5A-encoded cardiac sodium channel in patients referred for Brugada syndrome genetic testing за авторством Jamie D. Kapplinger, David J. Tester, Mariëlle Alders, Begoña Benito, Myriam Berthet, Josép Brugada, Pedro Brugada, Véronique Fressart, Alejandra Guerchicoff, Carole Harris‐Kerr, Shiro Kamakura, Florence Kyndt, Tamara T. Koopmann, Yoshihiro Miyamoto, Ryan Pfeiffer, Guido D. Pollevick, Vincent Probst, Sven Zumhagen, Matteo Vatta, Jeffrey A. Towbin, Wataru Shimizu, Eric Schulze‐Bahr, Charles Antzelevitch, Benjamin A. Salisbury, Pascale Guicheney, Arthur A.M. Wilde, Ramón Brugada, Jean‐Jacques Schott, Michael J. Ackerman

    Опубліковано 2009
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  18. 18
    New insights into mitral valve dystrophy: a Filamin-A genotype–phenotype and outcome study

    New insights into mitral valve dystrophy: a Filamin-A genotype–phenotype and outcome study за авторством Thierry Le Tourneau, Solena Le Scouarnec, Caroline Cueff, Daniel Bernstein, Jan J.J. Aalberts, Simon Lecointe, Jean Mérot, Jonathan A. Bernstein, Toon Oomen, Christian Dina, Matilde Karakachoff, Hubert Desal, Ousama Al Habash, Francesca N. Delling, Romain Capoulade, Albert J.H. Suurmeijer, David J. Milan, Russell A. Norris, Roger R. Markwald, Elena Aïkawa, Susan A. Slaugenhaupt, Xavier Jeunemaı̂tre, Albert Hagège, Jean-Christian Roussel, Jean‐Noël Trochu, Robert A. Levine, Florence Kyndt, Vincent Probst, Hervé Le Marec, Jean‐Jacques Schott

    Опубліковано 2017
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  19. 19
    Genetic association analyses highlight biological pathways underlying mitral valve prolapse

    Genetic association analyses highlight biological pathways underlying mitral valve prolapse за авторством Christian Dina, Nabila Bouatia‐Naji, Nathan R. Tucker, Francesca N. Delling, Katelynn Toomer, Ronen Durst, M. Perrocheau, Leticia Fernández‐Friera, Jorge Solı́s, Thierry Le Tourneau, Ming‐Huei Chen, Vincent Probst, Yohan Bossé, Philippe Pîbarot, Diana Zélénika, Mark Lathrop, Serge Herçberg, Ronan Roussel, Emelia J. Benjamin, Fabrice Bonnet, Su Hao Lo, Elena Dolmatova, Floriane Simonet, Simon Lecointe, Florence Kyndt, Richard Redon, Hervé Le Marec, Philippe Froguel, Patrick T. Ellinor, Ramachandran S. Vasan, Patrick Bruneval, Roger R. Markwald, Russell A. Norris, David J. Milan, Susan Slaugenhaupt, Robert A. Levine, Jean‐Jacques Schott, Albert Hagège, Xavier Jeunemaı̂tre

    Опубліковано 2015
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  20. 20
    TAD boundary deletion causes PITX2-related cardiac electrical and structural defects

    TAD boundary deletion causes PITX2-related cardiac electrical and structural defects за авторством Manon Baudic, Hiroshige Murata, Fernanda M. Bosada, Uirá Souto Melo, Takanori Aizawa, Pierre Lindenbaum, Lieve E. van der Maarel, Amaury Guedon, Estelle Baron, Enora Fremy, Adrien Foucal, Taisuke Ishikawa, Hiroya Ushinohama, Sean J. Jurgens, Seung Hoan Choi, Florence Kyndt, Solena Le Scouarnec, Vincent Wakker, Aurélie Thollet, A Rajalu, Tadashi Takaki, Seiko Ohno, Wataru Shimizu, Minoru Horie, Takeshi Kimura, Patrick T. Ellinor, Florence Petit, Yves Dulac, Paul Bru, Anne Boland, Jean‐François Deleuze, Richard Redon, Hervé Le Marec, Thierry Le Tourneau, Jean‐Baptiste Gourraud, Yoshinori Yoshida, Naomasa Makita, C Vieyres, Takeru Makiyama, Stefan Mundlos, Vincent M. Christoffels, Vincent Probst, Jean‐Jacques Schott, Julien Barc

    Опубліковано 2024
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