Zobrazeno 1 - 10
of 150
pro vyhledávání: '"Ari Chaouat"'
Publikováno v:
Frontiers in Medicine, Vol 11 (2024)
Pulmonary arterial hypertension (PAH) is characterized by a progressive increase in pulmonary vascular resistance (PVR) due to vascular remodeling of the small pulmonary arteries. In advanced RV failure or severe hypoxemia, extra corporeal life suppo
Externí odkaz:
https://doaj.org/article/9bac9fae8e304c29917b5786855f1fec
Autor:
Athénaïs Boucly, Sabina Solinas, Antoine Beurnier, Xavier Jaïs, Sophia Keddache, Mélanie Eyries, Andrei Seferian, Mitja Jevnikar, Anne Roche, Sophie Bulifon, Arnaud Bourdin, Ari Chaouat, Vincent Cottin, Laurent Bertoletti, Laurent Savale, Marc Humbert, Olivier Sitbon, David Montani
Publikováno v:
ERJ Open Research, Vol 10, Iss 1 (2024)
Introduction Pulmonary veno-occlusive disease (PVOD) is a rare and severe subtype of pulmonary arterial hypertension (PAH). Although European Society of Cardiology/European Respiratory Society (ESC/ERS) guidelines advise assessing PAH severity at bas
Externí odkaz:
https://doaj.org/article/a3a5886fc8314a5fa2fce871c4885790
Publikováno v:
Swiss Medical Weekly, Vol 152, Iss 0506 (2022)
Pulmonary hypertension is an heterogeneous group of diseases characterised by increased pulmonary arterial pressures which impact on the upstream right ventricle. Pulmonary hypertension can be challenging to diagnose, classify and monitor when specif
Externí odkaz:
https://doaj.org/article/7ce3b29767a1429787a9e77192795fe4
Autor:
Morgane Faure, MD, Emmanuel Gomez, MD, Peter Dorfmüller, MD, PhD, Damien Mandry, MD, PhD, Matthieu Canuet, Romain Kessler, François Chabot, Ari Chaouat, MD, PhD
Publikováno v:
Respiratory Medicine Case Reports, Vol 21, Iss C, Pp 74-77 (2017)
Pulmonary veno-occlusive disease is characterized by remodeling of pulmonary arteries, capillaries and venules. We report a case of diffuse lung emphysema and pulmonary veno-occlusive disease with the characteristic of having no airflow limitation. A
Externí odkaz:
https://doaj.org/article/4165ff9aec344b2a9308adb4d72d2700
Autor:
Sabine Revuz, Evelyne Decullier, Isabelle Ginon, Nicolas Lamblin, Pierre-Yves Hatron, Pierre Kaminsky, Marie-France Carette, Pascal Lacombe, Anne-Claire Simon, Sophie Rivière, Jean-Robert Harlé, Alain Fraisse, Christian Lavigne, Vanessa Leguy-Seguin, Ari Chaouat, Chahera Khouatra, Sophie Dupuis-Girod, Eric Hachulla
Publikováno v:
PLoS ONE, Vol 12, Iss 10, p e0184227 (2017)
Different pulmonary hypertension (PH) mechanisms are associated with hereditary haemorrhagic telangiectasia (HHT).We conducted a retrospective study of all suspected cases of PH (echocardiographically estimated systolic pulmonary artery pressure [sPA
Externí odkaz:
https://doaj.org/article/9fbe1814329f4108896a85e2d1ca701b
Autor:
David Montani, Laurent Bertoletti, Marie-Camille Chaumais, Swanny Perrin, Dominique Fabre, Ari Chaouat, Xavier Jaïs, Gérald Simonneau, Marc Humbert
Publikováno v:
European Respiratory Review, Vol 23, Iss 132, Pp 260-263 (2014)
Externí odkaz:
https://doaj.org/article/4563adbe98a64cee9228f0ff9ccfedb0
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:
Simon Valentin, Brian Renel, Florian Manneville, Bénédicte Caron, Myriam Choukour, Anne Guillaumot, Ari Chaouat, Mathias Poussel, Thomas Chateau, Carina Peyrin-Biroulet, Hamza Achit, Laurent Peyrin-Biroulet, François Chabot
Publikováno v:
Inflammatory Bowel Diseases. 29:207-216
Background No large, prospective study has investigated respiratory symptoms in patients with inflammatory bowel diseases. We aimed to describe the prevalence of and factors associated with respiratory symptoms in patients with inflammatory bowel dis
Autor:
Pierre Thoré, Jean Staentzel, Simon Valentin, Anne Guillaumot, Christine Selton-Suty, Emmanuel Gomez, François Chabot, Ari Chaouat
Publikováno v:
Respiratory Medicine and Research. 83:101008
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