Rezultaty - Lecointe, Simon

Non-syndromic Mitral Valve Dysplasia Mutation Changes the Force Resilience and Interaction of Human Filamin A od Haataja, Tatu J.K., Bernardi, Rafael C., Lecointe, Simon, Capoulade, Romain, Merot, Jean, Pentikäinen, Ulla

Dokumenty pełnotekstowe Dokumenty pełnotekstowe Dokumenty pełnotekstowe

Critical Structural Defects Explain Filamin A Mutations Causing Mitral Valve Dysplasia od Haataja, Tatu J.K., Capoulade, Romain, Lecointe, Simon, Hellman, Maarit, Merot, Jean, Permi, Perttu, Pentikäinen, Ulla

Dokumenty pełnotekstowe Dokumenty pełnotekstowe Dokumenty pełnotekstowe

Fine-scale human genetic structure in Western France od Karakachoff, Matilde, Duforet-Frebourg, Nicolas, Simonet, Floriane, Le Scouarnec, Solena, Pellen, Nadine, Lecointe, Simon, Charpentier, Eric, Gros, Françoise, Cauchi, Stéphane, Froguel, Philippe, Copin, Nane, Le Tourneau, Thierry, Probst, Vincent, Le Marec, Hervé, Molinaro, Sabrina, Balkau, Beverley, Redon, Richard, Schott, Jean-Jacques, Blum, Michael GB, Dina, Christian

Dokumenty pełnotekstowe Dokumenty pełnotekstowe Dokumenty pełnotekstowe

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

Dokumenty pełnotekstowe Dokumenty pełnotekstowe Dokumenty pełnotekstowe

Genetic association analyses highlight biological pathways underlying mitral valve prolapse od Dina, Christian, Bouatia-Naji, Nabila, Tucker, Nathan, Delling, Francesca N., Toomer, Katelynn, Durst, Ronen, Perrocheau, Maelle, Fernandez-Friera, Leticia, Solis, Jorge, Le Tourneau, Thierry, Chen, Ming-Huei, Probst, Vincent, Bosse, Yohan, Pibarot, Philippe, Zelenika, Diana, Lathrop, Mark, Hercberg, Serge, Roussel, Ronan, Benjamin, Emelia J., Bonnet, Fabrice, Su Hao, LO, Dolmatova, Elena, Simonet, Floriane, Lecointe, Simon, Kyndt, Florence, Redon, Richard, Le Marec, Hervé, Froguel, Philippe, Ellinor, Patrick T., Vasan, Ramachandran S., Bruneval, Patrick, Norris, Russell A., Milan, David J., Slaugenhaupt, Susan A., Levine, Robert A., Schott, Jean-Jacques, Hagege, Albert A., Jeunemaitre, Xavier

Dokumenty pełnotekstowe Dokumenty pełnotekstowe Dokumenty pełnotekstowe

Common variants at SCN5A-SCN10A and HEY2 are associated with Brugada syndrome, a rare disease with high risk of sudden cardiac death od 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, Olesen, Morten Salling, Kääb, Stefan, Beckmann, Britt M., Weeke, Peter, Watanabe, Hiroshi, Endo, Naoto, Minamino, Tohru, Horie, Minoru, Ohno, Seiko, Hasegawa, Kanae, Makita, Naomasa, Nogami, Akihiko, Shimizu, Wataru, Aiba, Takeshi, Froguel, Philippe, Balkau, Beverley, Lantieri, Olivier, Torchio, Margherita, Wiese, Cornelia, Weber, David, Wolswinkel, Rianne, Coronel, Ruben, Boukens, Bas J., Bézieau, Stéphane, Charpentier, Eric, Chatel, Stéphanie, Despres, Aurore, Gros, Françoise, Kyndt, Florence, Lecointe, Simon, Lindenbaum, Pierre, Portero, Vincent, Violleau, Jade, Gessler, Manfred, Tan, Hanno L., Roden, Dan M., Christoffels, Vincent M., Le Marec, Hervé, Wilde, Arthur A, Probst, Vincent, Schott, Jean-Jacques, Dina, Christian, Redon, Richard

Dokumenty pełnotekstowe Dokumenty pełnotekstowe Dokumenty pełnotekstowe