Zobrazeno 1 - 10
of 19
pro vyhledávání: '"Lidwine Wémeau"'
Autor:
Raphael Borie, Caroline Kannengiesser, Laurent Gouya, Clairelyne Dupin, Serge Amselem, Ibrahima Ba, Vincent Bunel, Philippe Bonniaud, Diane Bouvry, Aurélie Cazes, Annick Clement, Marie Pierre Debray, Philippe Dieude, Ralph Epaud, Pascale Fanen, Elodie Lainey, Marie Legendre, Aurélie Plessier, Flore Sicre de Fontbrune, Lidwine Wemeau-Stervinou, Vincent Cottin, Nadia Nathan, Bruno Crestani
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 14, Iss 1, Pp 1-10 (2019)
Abstract Background Genetic testing is proposed for suspected cases of monogenic pulmonary fibrosis, but clinicians and patients need specific information and recommendation about the related diagnosis and management issues. Because multidisciplinary
Externí odkaz:
https://doaj.org/article/8636ea4a4a5f4fc7add9b69396ed22b1
Autor:
Cécile Chenivesse, Sarah Gephine, Martin Dornbierer, Victor Valentin, Olivier Le Rouzic, Lidwine Wémeau, Jean-Marie Grosbois
Publikováno v:
ERJ Open Research, Vol 10, Iss 1 (2024)
Background Our objective was to evaluate the short-, medium- and long-term benefits of home-based pulmonary rehabilitation (PR) on the physical and affective components of dyspnoea in people with fibrotic idiopathic interstitial pneumonias (f-IIPs).
Externí odkaz:
https://doaj.org/article/075f188070cf47d492dab425b5f56fa1
Publikováno v:
Therapeutic Advances in Respiratory Disease, Vol 12 (2018)
Background: Although the 6-min walk test (6MWT) is the gold standard for assessing exercise-induced impairment of gas exchange, it cannot easily be performed in a clinical office environment. The aim of this study was to compare the 1-min sit-to-stan
Externí odkaz:
https://doaj.org/article/e52cacb26f7a4e57b59d8e10ff9392dd
Autor:
Benoit Wallaert, Nicolas Masson, Olivier Le Rouzic, Baptiste Chéhère, Lidwine Wémeau-Stervinou, Jean-Marie Grosbois
Publikováno v:
ERJ Open Research, Vol 4, Iss 2 (2018)
Externí odkaz:
https://doaj.org/article/2de6f148c6af4029a8915584b62299bf
Autor:
Nadia Sivova, David Launay, Lidwine Wémeau-Stervinou, Pascal De Groote, Martine Remy-Jardin, Guillaume Denis, Marc Lambert, Nicolas Lamblin, Sandrine Morell-Dubois, Marie Fertin, Guillaume Lefevre, Vincent Sobanski, Olivier Le Rouzic, Pierre-Yves Hatron, Benoit Wallaert, Eric Hachulla, Thierry Perez
Publikováno v:
PLoS ONE, Vol 8, Iss 10, p e78001 (2013)
We investigated whether partitioning DLCO into membrane conductance for CO (DmCO) and pulmonary capillary blood volume (Vcap) was helpful in suspecting precapillary pulmonary (arterial) hypertension (P(A)H) in systemic sclerosis (SSc) patients with o
Externí odkaz:
https://doaj.org/article/67bba24709b94dec902f77b449bf9cf0
Autor:
Nathan Hennion, Jean-Luc Desseyn, Frédéric Gottrand, Lidwine Wémeau-Stervinou, Valérie Gouyer
Publikováno v:
médecine/sciences
médecine/sciences, 2022, Medecine sciences : M/S, 38 (6-7), pp.579-584. ⟨10.1051/medsci/2022084⟩
médecine/sciences, 2022, Medecine sciences : M/S, 38 (6-7), pp.579-584. ⟨10.1051/medsci/2022084⟩
Idiopathic pulmonary fibrosis (IPF) is a chronic, progressive and fatal lung disease of unknown origin. It is characterized by aberrant scarring of the alveolar epithelium leading to an accumulation of extracellular matrix (ECM). Fibroblastic foci, c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a08f1ebd8ce523720d99bda46aa28d0c
https://doi.org/10.1051/medsci/2022084
https://doi.org/10.1051/medsci/2022084
Autor:
Paul Decker, Vincent Sobanski, Thomas Moulinet, David Launay, Eric Hachulla, Victor Valentin, Benoit Godbert, Sabine Revuz, Anne Guillaumot, Emmanuel Gomez, François Chabot, Lidwine Wémeau, Roland Jaussaud
Publikováno v:
European Journal of Internal Medicine. 97:62-68
Among interstitial pneumonia with autoimmune features (IPAF) patients, identifying those at risk to develop a connective tissue disease (CTD) during the disease course is a key issue. The aim of this study was to evaluate the incidence of definite CT
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::da786ffa2e8bccbb47db86c4ac58314e
https://doi.org/10.1016/j.ejim.2021.12.021
https://doi.org/10.1016/j.ejim.2021.12.021
Autor:
Vincent Cottin, Philippe Bonniaud, Jacques Cadranel, Bruno Crestani, Stéphane Jouneau, Sylvain Marchand-Adam, Hilario Nunes, Lidwine Wémeau-Stervinou, Emmanuel Bergot, Elodie Blanchard, Raphaël Borie, Arnaud Bourdin, Cécile Chenivesse, Annick Clément, Emmanuel Gomez, Anne Gondouin, Sandrine Hirschi, François Lebargy, Charles-Hugo Marquette, David Montani, Grégoire Prévot, Sébastien Quetant, Martine Reynaud-Gaubert, Mathieu Salaun, Olivier Sanchez, Bruno Trumbic, Karim Berkani, Pierre-Yves Brillet, Marion Campana, Lara Chalabreysse, Gérard Chatté, Didier Debieuvre, Gilbert Ferretti, Jean-Michel Fourrier, Nicolas Just, Marianne Kambouchner, Bertrand Legrand, Frédéric Le Guillou, Jean-Pierre Lhuillier, Anas Mehdaoui, Jean-Marc Naccache, Catherine Paganon, Martine Rémy-Jardin, Salim Si-Mohamed, Philippe Terrioux
Publikováno v:
Respiratory Medicine and Research
Respiratory Medicine and Research, 2022, 39 (7), TT-Recommandations pratiques pour le diagnostic et la prise en charge de la fibrose. ⟨10.1016/j.resmer.2022.100948⟩
Respiratory Medicine and Research, 2022, 39 (7), TT-Recommandations pratiques pour le diagnostic et la prise en charge de la fibrose. ⟨10.1016/j.resmer.2022.100948⟩
National audience; BACKGROUND: Since the previous French guidelines were published in 2017, substantial additional knowledge about idiopathic pulmonary fibrosis has accumulated. METHODS: Under the auspices of the French-speaking Learned Society of Pu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7b12b9007dbe452b3bba6074202c27a3
https://hal.science/hal-04087431
https://hal.science/hal-04087431
Autor:
Julie Mankikian, Agnès Caille, Martine Reynaud-Gaubert, Marie-Sara Agier, Julien Bermudez, Philippe Bonniaud, Raphael Borie, Pierre-Yves Brillet, Jacques Cadranel, Isabelle Court-Fortune, Bruno Crestani, Marie-Pierre Debray, Emmanuel Gomez, Anne Gondouin, Sandrine Hirschi-Santelmo, Dominique Israel-Biet, Stéphane Jouneau, Karine Juvin, Julie Leger, Mallorie Kerjouan, Charles-Hugo Marquette, Jean-Marc Naccache, Hilario Nunes, Laurent Plantier, Grégoire Prevot, Sébastien Quetant, Julie Traclet, Victor Valentin, Yurdagul Uzunhan, Lidwine Wémeau-Stervinou, Theodora Bejan-Angoulvant, Vincent Cottin, Sylvain Marchand-Adam
Publikováno v:
European Respiratory Journal
European Respiratory Journal, 2023, 61, pp.2202071. ⟨10.1183/13993003.02071-2022⟩
European Respiratory Journal, 2023, 61, pp.2202071. ⟨10.1183/13993003.02071-2022⟩
BackgroundStandard of care for interstitial lung disease (ILD) with a nonspecific interstitial pneumonia (NSIP) pattern proposes mycophenolate mofetil (MMF) as one of the first step therapies while rituximab is used as rescue therapy.MethodsIn a rand
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2e80754f405876afd906de2f27c682a3
https://doi.org/10.1183/13993003.02071-2022
https://doi.org/10.1183/13993003.02071-2022
Autor:
François Lestelle, Catherine Beigelman, David Rotzinger, Salim Si-Mohamed, Mouhamad Nasser, Lidwine Wemeau, Sandrine Hirschi, Grégoire Prevot, Antoine Roux, Vincent Bunel, Emmanuel Gomez, Laurent Sohier, Helene Morisse Pradier, Martine Reynaud Gaubert, Anne Gondouin, Romain Lazor, Jean-Charles Glerant, Françoise Thivolet Bejui, Magali Colombat, Vincent Cottin, the OrphaLung network
Publikováno v:
Respiratory Research, Vol 25, Iss 1, Pp 1-12 (2024)
Abstract Background Light chain deposition disease (LCDD) is a very rare entity. Clinical manifestations of LCDD vary according to the organs involved. Data on pulmonary LCDD are scarce and limited to small series or case reports. This study aimed to
Externí odkaz:
https://doaj.org/article/fba51a8eb5a4463791e31e0e1411e6c3