Zobrazeno 1 - 10
of 22
pro vyhledávání: '"Pascal Magro"'
Autor:
Thi Thao Truc Le, Guillaume Martinent, Sophie Dupuis-Girod, Antoine Parrot, Anne Contis, Sophie Riviere, Thierry Chinet, Vincent Grobost, Olivier Espitia, Brigitte Dussardier-Gilbert, Laurent Alric, Guillaume Armengol, Hélène Maillard, Vanessa Leguy-Seguin, Sylvie Leroy, Murielle Rondeau-Lutz, Christian Lavigne, Shirine Mohamed, Laurent Chaussavoine, Pascal Magro, Julie Seguier, Mallorie Kerjouan, Sylvie Fourdrinoy
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 17, Iss 1, Pp 1-14 (2022)
Abstract Background Hereditary hemorrhagic telangiectasia (HHT) disease is a rare genetic disorder with symptoms and complications that can significantly affect patients’ daily lives. To date, no scale has been validated to assess the specific symp
Externí odkaz:
https://doaj.org/article/cecf83f4ed6f4dbb8475401e0e67d5cb
Autor:
Xavier Jaïs, Philippe Brenot, Hélène Bouvaist, Mitja Jevnikar, Matthieu Canuet, Céline Chabanne, Ari Chaouat, Vincent Cottin, Pascal De Groote, Nicolas Favrolt, Delphine Horeau-Langlard, Pascal Magro, Laurent Savale, Grégoire Prévot, Sébastien Renard, Olivier Sitbon, Florence Parent, Romain Trésorier, Cécile Tromeur, Céline Piedvache, Lamiae Grimaldi, Elie Fadel, David Montani, Marc Humbert, Gérald Simonneau
Publikováno v:
The Lancet Respiratory Medicine. 10:961-971
Autor:
Vincent Cottin, David Montani, Jérémie Pichon, Martine Reynaud-Gaubert, Xavier Jaïs, Pascal Magro, Gérald Simonneau, Florence Parent, Fabrice Bauer, Marianne Riou, Laurent Bertoletti, Pamela Moceri, Ari Chaouat, Andrei Seferian, Antoine Beurnier, Sébastien Renard, Pierre Mauran, Delphine Horeau-Langlard, Pascal de Groote, Laurent Savale, Mitja Jevnikar, Sophie Bulifon, Pascal Roblot, Hélène Bouvaist, Yuanchao Feng, Patrice Poubeau, Sylvain Palat, Zhiying Liang, Emmanuel Bergot, François Picard, Etienne-Marie Jutant, C. Chabanne, Olivier Sitbon, Athénaïs Boucly, Grégoire Prévot, Jean-François Mornex, Cécile Tromeur, Marc Humbert, Bruno Degano, Claire Dauphin, Arnaud Bourdin, Olivier Sanchez, Nicolas Favrolt, Jason Weatherald
Publikováno v:
American Journal of Respiratory and Critical Care Medicine
American Journal of Respiratory and Critical Care Medicine, American Thoracic Society, 2021, 204 (7), pp.842-854. ⟨10.1164/rccm.202009-3698OC⟩
American Journal of Respiratory and Critical Care Medicine, 2021, 204 (7), pp.842-854. ⟨10.1164/rccm.202009-3698OC⟩
American Journal of Respiratory and Critical Care Medicine, American Thoracic Society, 2021, 204 (7), pp.842-854. ⟨10.1164/rccm.202009-3698OC⟩
American Journal of Respiratory and Critical Care Medicine, 2021, 204 (7), pp.842-854. ⟨10.1164/rccm.202009-3698OC⟩
International audience; Rationale: The relationship between the initial treatment strategy and survival in pulmonary arterial hypertension (PAH) remains uncertain. Objectives: To evaluate the long-term survival of patients with PAH categorized accord
Autor:
François Durand, Laurent Savale, Clément Boissin, Olivier Sitbon, Claire Francoz, Hélène Bouvaist, Jean-Charles Duclos-Vallée, Ari Chaouat, Manuel Guimas, Pamela Moceri, Emmanuel Bergot, Pascal Magro, David Montani, Nicolas Lamblin, Vincent Cottin, Marianne Riou, Filomena Conti, Marc Humbert, Nicolas Favrolt, Romain Trésorier, Xavier Jaïs, Sébastien Renard, Philippe Hervé, Grégoire Prévot, Cécile Tromeur, Bruno Degano, Céline Chabanne, Delphine Bourlier, Nathan Ebstein, Sylvain Palat, Didier Samuel, Gérald Simonneau, Elise Artaud-Macari, Delphine Horeau-Langlard, Pascal de Groote, Anne-Claire Simon, Mitja Jevnikar, Audrey Coilly, Marie Fertin
Publikováno v:
Journal of Hepatology. 73:130-139
Background & Aims Long-term outcomes in portopulmonary hypertension (PoPH) are poorly studied in the current era of pulmonary hypertension management. We analysed the effect of pulmonary arterial hypertension (PAH)-targeted therapies, survival and pr
Autor:
Montani, David, Certain, Marie-Caroline, Weatherald, Jason, Jaïs, Xavier, Bulifon, Sophie, Noel-Savina, Elise, Nieves, Ana, Renard, Sébastien, Traclet, Julie, Bouvaist, Hélène, Riou, Marianne, de Groote, Pascal, Moceri, Pamela, Bertoletti, Laurent, Favrolt, Nicolas, Guillaumot, Anne, Jutant, Etienne-Marie, Beurnier, Antoine, Boucly, Athénaïs, Ebstein, Nathan, Jevnikar, Mitja, Pichon, Jérémie, Keddache, Sophia, Preda, Mariana, Roche, Anne, Solinas, Sabina, Seferian, Andrei, Reynaud-Gaubert, Martine, Cottin, Vincent, Savale, Laurent, Humbert, Marc, Sitbon, Olivier, Kais, Ahmad, Elise, Artaud-Macari, Céline, Chabanne, Ari, Chaouat, Surnameclaire, Dauphin, Frédéric, Gagnadoux, Anne, Gaudoin, Sébastien, Hascoet, Delphine, Horeau-Langlard, Jocelyn, Inamo, Bouchra, Lamia, Pascal, Magro, Jean-Claude, Meurice, Patrice, Poubeau, Grégoire, Prevot, Roger, Rosario, Servettaz, Amélie
Publikováno v:
American journal of respiratory and critical care medicine, 206(5):573-583
American Journal of Respiratory and Critical Care Medicine
American Journal of Respiratory and Critical Care Medicine, 2022, 206 (5), pp.573-583. ⟨10.1164/rccm.202112-2761OC⟩
American Journal of Respiratory and Critical Care Medicine
American Journal of Respiratory and Critical Care Medicine, 2022, 206 (5), pp.573-583. ⟨10.1164/rccm.202112-2761OC⟩
International audience; Rationale: Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection is associated with pulmonary endothelial dysfunction. There are limited data available on the outcomes of coronavirus disease (COVID-19) in pati
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9c75208c13096f536e897045ff2f1d9f
https://www.atsjournals.org/doi/suppl/10.1164/rccm.202112-2761OC
https://www.atsjournals.org/doi/suppl/10.1164/rccm.202112-2761OC
Autor:
Alexandre Guilhem, Sophie Dupuis-Girod, Olivier Espitia, Sophie Rivière, Julie Seguier, Mallorie Kerjouan, Christian Lavigne, Hélène Maillard, Pascal Magro, Laurent Alric, Dan Lipsker, Antoine Parrot, Vanessa Leguy, Claire Vanlemmens, Laurent Guibaud, Miikka Vikkula, Melanie Eyries, Pierre-Jean Valette, Sophie Giraud
Publikováno v:
Journal of Medical Genetics. :jmg-2022
BackgroundEPHB4loss of function is associated with type 2 capillary malformation–arteriovenous malformation syndrome, an autosomal dominant vascular disorder. The phenotype partially overlaps with hereditary haemorrhagic telangiectasia (HHT) due to
Autor:
Pamela Moceri, Maria-Rosa Ghigna, Olivier Sitbon, Céline Chabanne, Marc Humbert, Pascal de Groote, Pierre Wolkenstein, Julie Traclet, Xavier Mignard, Emmanuel Bergot, François Goupil, Delphine Bourlier, Xavier Jaïs, Etienne-Marie Jutant, David Montani, Frédéric Perros, Laurent Bertoletti, Jean-Pierre Gueffet, Gérald Simonneau, Thibaud Soumagne, Nicolas Favrolt, Grégoire Prévot, Cécile Tromeur, Pierre-Yves Brillet, Barbara Girerd, Mitja Jevnikar, Fabrice Bauer, Ari Chaouat, Pascal Magro, Raphael Borie, Elie Fadel, Laurent Savale, Claire Dauphin
Publikováno v:
American journal of respiratory and critical care medicine. 202(6)
Rationale: Pulmonary hypertension (PH) associated with neurofibromatosis type 1 (NF1) is a rare and largely unknown complication of NF1.Objectives: To describe characteristics and outcomes of PH-NF...
Autor:
Pascal Magro, E. Laurent, Ephrem Salamé, Camille Besh, Sébastien Dharancy, Christophe Bureau, Frédéric Patat, Jérôme Dumortier, Armand Abergel, Marie-Lorraine Woehl Jaegle, Georges-Philippe Pageaux, Louise Barbier, Jean-Marc Perarnau, Claire Vanlemmens, Maud Reymond
Publikováno v:
Transplantation
Transplantation, 2018, 102 (4), pp.616--622. ⟨10.1097/TP.0000000000001981⟩
Transplantation, 2018, 102 (4), pp.616--622. ⟨10.1097/TP.0000000000001981⟩
International audience; Portopulmonary hypertension is defined by the presence of pulmonary arterial hypertension associated with portal hypertension. Its presence is a major stake for cirrhotic patients requiring liver transplantation (LT), with inc
Autor:
Fabrice Bauer, Laurent Bertoletti, Nicolas Favrolt, Laurent Savale, Florent Soubrier, Maria-Rosa Ghigna, Emmanuel Bergot, Etienne-Marie Jutant, Pamela Moceri, Xavier Jaïs, Gérald Simonneau, Pascal Degroote, Xavier Mignard, Pascal Magro, David Montani, Delphine Bourlier, Grégoire Prévot, Cécile Tromeur, Barbara Girerd, Olivier Sitbon, Marc Humbert, Julie Traclet, Pierre-Yves Brillet, Cécile Chabanne, Thibaud Soumagne, Claire Dauphin
Publikováno v:
Pulmonary hypertension.
Introduction: Pulmonary hypertension associated with neurofibromatosis type 1 (PH-NF1) is a rare but severe complication of NF1. The largest study about PH-NF1 described 8 patients and there are few data about outcomes on PH treatment. Methods: We re
Autor:
Christophe Pison, Anne Claire Simon, Pascal Magro, Gérald Simonneau, Céline Chabanne, Olivier Sitbon, Hélène Bouvaist, Carlos Garcia Alonso, Laurent Savale, Mitja Jevnikar, Romain Trésorier, Marc Humbert, Florence Parent, Philippe Brenot, Elie Fadel, Celine Piedvache, Grégoire Prévot, Cécile Tromeur, Delphine Horeau-Langlard, Hélène Agostini, Sébastien Renard, Nicolas Favrolt, Xavier Jaïs, Ari Chaouat, Matthieu Canuet, Pascal de Groote, David Montani, Vincent Cottin, Benoit Gerardin, Claire Dromer
Publikováno v:
Pulmonary hypertension.
Background: Medical therapy with riociguat and balloon pulmonary angioplasty (BPA) are two therapeutic options for inoperable chronic thromboembolic pulmonary hypertension (CTEPH). Controlled studies comparing these two treatments are lacking. Method