Zobrazeno 1 - 10
of 995
pro vyhledávání: '"A Calender"'
Autor:
Cottin, Vincent, Blanchard, Elodie, Kerjouan, Mallorie, Lazor, Romain, Reynaud-Gaubert, Martine, Taille, Camille, Uzunhan, Yurdagül, Wemeau, Lidwine, Andrejak, Claire, Baud, Dany, Bonniaud, Philippe, Brillet, Pierre-Yves, Calender, Alain, Chalabreysse, Lara, Court-Fortune, Isabelle, Desbaillets, Nicolas Pierre, Ferretti, Gilbert, Guillemot, Anne, Hardelin, Laurane, Kambouchner, Marianne, Leclerc, Violette, Lederlin, Mathieu, Malinge, Marie-Claire, Mancel, Alain, Marchand-Adam, Sylvain, Maury, Jean-Michel, Naccache, Jean-Marc, Nasser, Mouhamad, Nunes, Hilario, Pagnoux, Gaële, Prévot, Grégoire, Rousset-Jablonski, Christine, Rouviere, Olivier, Si-Mohamed, Salim, Touraine, Renaud, Traclet, Julie, Turquier, Ségolène, Vagnarelli, Stéphane, Ahmad, Kaïs
Publikováno v:
In Respiratory Medicine and Research June 2023 83
Akademický článek
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Publikováno v:
In Trends in Immunology October 2020 41(10):856-859
Autor:
Pacheco, Yves, Lim, Clarice X., Weichhart, Thomas, Valeyre, Dominique, Bentaher, Abderrazzak, Calender, Alain
Publikováno v:
In Trends in Immunology April 2020 41(4):286-299
Autor:
Sophie Giraud, Claire Bardel, Sophie Dupuis-Girod, Marie-France Carette, Brigitte Gilbert-Dussardier, Sophie Riviere, Jean-Christophe Saurin, Mélanie Eyries, Sylvie Patri, Evelyne Decullier, Alain Calender, Gaëtan Lesca
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 15, Iss 1, Pp 1-7 (2020)
Abstract Background Hereditary Hemorrhagic Telangiectasia (HHT) is an autosomal dominant disorder characterized by multiple telangiectases and caused by germline disease-causing variants in the ENG (HHT1), ACVRL1 (HHT2) and, to a lesser extent MADH4
Externí odkaz:
https://doaj.org/article/6cb683a8210448e4a726913c553472f1
Autor:
Nathan, Nadia, Sileo, Chiara, Calender, Alain, Pacheco, Yves, Rosental, Paul-André, Cavalin, Catherine, Macchi, Odile, Valeyre, Dominique, Clement, Annick
Publikováno v:
In Paediatric Respiratory Reviews February 2019 29:53-59
Publikováno v:
Rheumatology; Jun2024, Vol. 63 Issue 6, p1512-1517, 6p
Autor:
Alain Calender, Pierre Antoine Rollat Farnier, Adrien Buisson, Stéphane Pinson, Abderrazzaq Bentaher, Serge Lebecque, Harriet Corvol, Rola Abou Taam, Véronique Houdouin, Claire Bardel, Pascal Roy, Gilles Devouassoux, Vincent Cottin, Pascal Seve, Jean-François Bernaudin, Clarice X. Lim, Thomas Weichhart, Dominique Valeyre, Yves Pacheco, Annick Clement, Nadia Nathan, in the frame of GSF (Groupe Sarcoïdose France)
Publikováno v:
BMC Medical Genomics, Vol 11, Iss 1, Pp 1-19 (2018)
Abstract Background Sarcoidosis (OMIM 181000) is a multi-systemic granulomatous disorder of unknown origin. Despite multiple genome-wide association (GWAS) studies, no major pathogenic pathways have been identified to date. To find out relevant sarco
Externí odkaz:
https://doaj.org/article/4056fb49f80d4471b504aa3aa69fdf58
Autor:
Valérie Besnard, Alain Calender, Diane Bouvry, Yves Pacheco, Catherine Chapelon-Abric, Florence Jeny, Hilario Nunes, Carole Planès, Dominique Valeyre
Publikováno v:
Respiratory Research, Vol 19, Iss 1, Pp 1-11 (2018)
Abstract Background Sarcoidosis is a systemic disease characterized by the formation of immune granulomas in various organs, mainly the lungs and the lymphatic system. Exaggerated granulomatous reaction might be triggered in response to unidentified
Externí odkaz:
https://doaj.org/article/91cd23916e5a4a898a54a2ff78ecadb5
Publikováno v:
In Bulletin du Cancer March 2017 104(3):288-294