Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Gérard Blaysat"'
Autor:
Gérard Blaysat
Publikováno v:
Archives of Cardiovascular Diseases Supplements. 2:126-131
Resume L’hypertension arterielle pulmonaire (HTAP) chez l’enfant est une pathologie severe. Le pronostic depend en grande partie de son etiologie. Le plus souvent l’HTAP est secondaire a une cardiopathie congenitale avec un shunt gauche-droite
Autor:
Annick Rossi, Hélène Moirot, Valérie Drouin-Garraud, Géraldine Joly-Helas, Pascale Saugier-Veber, Saad Abu Amara, Nathalie Le Meur, Thierry Frebourg, Alice Goldenberg, Stéphane Marret, Pascale Kleinfinger, Bertrand Mace, Gérard Blaysat, Christine Michel-Adde
Publikováno v:
American Journal of Medical Genetics Part A. :439-442
Holt-Oram syndrome, the major "heart-hand" syndrome is defined by the association of radial defects or triphalangeal thumbs and septal heart defects. The transmission is autosomal dominant and the causative gene has been shown to be TBX5, located on
Publikováno v:
Archives of Cardiovascular Diseases Supplements. 9:283
Publikováno v:
Archives of Cardiovascular Diseases Supplements. 8:v
Autor:
Paul Mulder, Gérard Blaysat, Pierre Desché, Elizabeth Scalbert, Vincent Richard, Jean-Paul Henry, Christian Thuillez, Patricia Compagnon, Lahcen Elfertak
Publikováno v:
American Journal of Hypertension. 8:7S-12S
Chronic heart failure (CHF) impairs endothelium-dependent vasodilatation of large conductance arteries. We investigated whether a similar reduction also occurs in small arteries, and whether such a reduction can be prevented by the angiotensin conver
Autor:
Saad Abu Amara, Marianne Alison, Juliette Andreu-Gallien, Francois Angoulvant, Jean-Baptiste Armengaud, Amine Arsan, Sonia Azib, Robin Azoulay, Sylvain Bailleux, Céline Bailly, Ananda Banerjee, Sébastien Barbarot, Laurent Bardiaux, Julien Baruteau, Clarisse Baumann, Nicole Beydon, Étienne Bidat, Édouard Bingen, Gérard Blaysat, Renaud Blondé, Cécile Boscher, Astrid Botte, Olivier Bourdon, Antoine Bourrillon, Olivia Boyer, Dominique Brémond-Gignac, Françoise Brion, Pierre Broué, Anne Cailho, Caroline Camby, Jean-Claude Carel, Brigitte Chabrol, Alain Chantepie, Frédérique Chedevergne, Gérard Chéron, Bertrand Chevallier, Didier Chevenne, Jean-Pierre Chouraqui, Robert Cohen, Paul Czernichow, Anne Dariel, Stéphane Dauger, Jacques de Blic, Stephan De Napoli Cocci, Dominique Debray, Christophe Delacourt, Georges Deschênes, Jean Donadieu, Claire Dossier, François Dubos, Jean-François Duhamel, Guy Dutau, Philippe Duverger, Didier Ernenwein, Albert Faye, Patrick Fellus, Marc Fila, Pierre Foucaud, Martine Fançois, Vincent Gajdos, Olivier Gall, Arnaud Garnier, Joël Gaudelus, Dominique Gendrel, Yves Gillet, Nadine Girard, Jean-Philippe Girardet, Nathalie Godon, Frédéric Gottrand, Véronique Gournay, Christèle Gras-Le Guen, Emmanuel Grimprel, Antoine Guédeney, Nicole Guédeney, Hervé Haas, Régis Hankard, Max Hassan, Véronique Hentgen, Xavier Hernandorena, Laurent Holvoet-Vermaut, Véronique Houdouin, Marie-Françoise Hurtaud-Roux, Brice Ilharreborde, Patrick Imbert, Paul Jacquin, Pierre-Henri Jarreau, Étienne Javouhey, Chantal Job-Deslandre, Isabelle Koné-Paut, Odile Kremp, Pauline Krug, Philippe Labrune, Marie Émilie Lampin, Élise Launay, Anne Lautridou, Muriel Le Bourgeois, Hervé Le Guen, Marie-France Le Heuzey, Gaëlle Le Henaff, Michel Lecendreux, Joël Lechevallier, Marc-David Leclair, Juliane Léger, Dominique Leroyer, Karine Levieux, Martine Levine, Jean-Michel Liet, David Lopes, Emmanuel Lopez, Gérard Lorette, Mathie Lorrot, Marie-Alice Macher, Éric Mallet, Martine Marchand, Valérie Marcou, Annabel Maruani, Pierre Mary, Karine Mention-Mulliez, Gérard Michel, Charlotte Michot, Mathieu Milh, Philippe Minodier, Isabelle Moraillon, Marie-Christine Mouren, Philippe Narcy, Sylvie N'guyen The Tich, Sophie Parat-Lesbros, Juliana Patkai, Yves Perel, Emilia Perrier-Cornet, Capucine Picard, Georges Picherot, Michel Polak, Sonia Prot-Labarthe, Geneviève Richard, Pierre Rochcongar, Pierre Rohrlich, Michel Roussey, Gwénaëlle Roussey-Kesler, Michel Rybojad, Didier Scavarda, Catherine Schlemmer, Guy Sebag, Anne-Laure Sellier-Leclerc, Isabelle Sermet-Gaudelus, Dominique Simon, Frédéric Sorge, Chantal Stheneur, Bogdana Tilea, Jean-Marc Treluyer, Nadia Tubiana-Rufi, Elena Tudorache, Nathalie Vabres, Thierry Van Den Abbeele, Anaïs Victor, Michel Vidailhet, Nathalie Villeneuve, Bénédicte Vrignaud, Sylvette Wiener-Vacher, Chantal Wood, Élodie Zana-Taieb, Delphine Zenaty
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::65bd9b62863b35b176aa8746932beca1
https://doi.org/10.1016/b978-2-294-71375-0.50038-6
https://doi.org/10.1016/b978-2-294-71375-0.50038-6
Autor:
Nathalie, Le Meur, Alice, Goldenberg, Christine, Michel-Adde, Valérie, Drouin-Garraud, Gérard, Blaysat, Stéphane, Marret, Saad Abu, Amara, Hélène, Moirot, Géraldine, Joly-Hélas, Bertrand, Mace, Pascale, Kleinfinger, Pascale, Saugier-Veber, Thierry, Frébourg, Annick, Rossi
Publikováno v:
American journal of medical genetics. Part A. 134(4)
Holt-Oram syndrome, the major "heart-hand" syndrome is defined by the association of radial defects or triphalangeal thumbs and septal heart defects. The transmission is autosomal dominant and the causative gene has been shown to be TBX5, located on
Autor:
Ba Luu Truong, Anne Moreau De Bellaing, Emmanuelle Vialle, Ayman Haydar, Pascal Vouhe, Pierre Simon Jouk, Gerard Blaysat
Publikováno v:
Frontiers in Pediatrics, Vol 8 (2020)
Aorto-left ventricular tunnel (ALVT) is a rare congenital heart defect. Surgery has to be performed early to avoid life-threatening complications. Prenatal diagnosis of this defect is challenging. We report a case of ALVT diagnosed in a fetus showing
Externí odkaz:
https://doaj.org/article/3e8d7410d6b04ea69aa4bd9857c083d2