Zobrazeno 1 - 10
of 109
pro vyhledávání: '"Gérard Lenoir"'
Autor:
Isabelle Sermet-Gaudelus, Muriel Le Bourgeois, Catherine Pierre-Audigier, Catherine Offredo, Didier Guillemot, Sophie Halley, Chantal Akoua-Koffi, Véronique Vincent, Valérie Sivadon-Tardy, Agnès Ferroni, Patrick Berche, Pierre Scheinmann, Gérard Lenoir, Jean-Louis Gaillard
Publikováno v:
Emerging Infectious Diseases, Vol 9, Iss 12, Pp 1587-1591 (2003)
We prospectively studied 298 patients with cystic fibrosis (mean age 11.3 years; range 2 months to 32 years; sex ratio, 0.47) for nontuberculous mycobacteria in respiratory samples from January 1, 1996, to December 31, 1999. Mycobacterium abscessus w
Externí odkaz:
https://doaj.org/article/e24773b263da473d99be451ace891983
Autor:
Wanda F. Reynolds, Isabelle Sermet-Gaudelus, Valérie Gausson, Marie-Noëlle Feuillet, Jean-Paul Bonnefont, Gérard Lenoir, Béatrice Descamps-Latscha, Véronique Witko-Sarsat
Publikováno v:
Mediators of Inflammation, Vol 2006 (2006)
The severity of cystic fibrosis (CF) pulmonary disease is not directly related to CFTR genotype but depends upon several parameters, including neutrophil-dominated inflammation. Identification of agents modulating inflammation constitutes a relevant
Externí odkaz:
https://doaj.org/article/1f07d9e8142449b582aab4e8004198b2
Autor:
Marie-Christine Vantyghem, Dominique Hubert, Andreas Claaß, Anne Munck, Doris Staab, Ute Staden, Helmut Teschler, Klaus-Michael Keller, Laurence Kessler, Horst Generlich, Guy-André Loeuille, Helen Mosnier-Pudar, Gabriela H. Thalhammer, Tanja Nickolay, Matthias V. Kopp, Nicole Prinz, Gérard Lenoir, Jürgen Hautz, Irmgard Eichler, Rüdiger Szczepanski, R Serreau, Jean-Jacques Robert, Hans-Georg Bresser, Birgit Schilling, Baroukh M. Assael, Martin Stern, Manfred Ballmann, Christina Smaczny, Egbert Herting, Matthias Wiebel, Lutz Naehrlich, Uwe Mellies, Hans-Georg Posselt, Ernst Rietschel, Thomas Biedermann, Thomas Köhnlein, Ernst-Hinrich Ballke, Wolfgang Kamin, Antje Schuster, Gerd Dockter, Holger Köster, Nathalie Wizla, Wolfram Wiebicke, Hans-Joachim Feickert, Manfred Götz, Sylvie Leroy, Marcus A Mall, Fawzia Aissat, Helge Hebestreit, Vera Wienhausen-Wilke, H.-E. Heuer, Isidor Huttegger, Alexandra Hebestreit, Raphaële Nove-Josserand, Laurence Weiss, Martin Claßen, Marguerite Honer, Reinhard W. Holl, Friedrich-Karl Tegtmeyer, Egbert Meyer, Peter Küster
Publikováno v:
The Lancet Diabetes & Endocrinology. 6:114-121
Summary Background As survival among patients with cystic fibrosis has improved in recent decades, complications have become increasingly relevant. The most frequent complication is cystic-fibrosis-related diabetes. The recommended treatment is injec
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6968bf741bada13505bd87c626a9e4be
https://doi.org/10.1016/s2213-8587(17)30400-x
https://doi.org/10.1016/s2213-8587(17)30400-x
Autor:
J. Djadi-Prat, Jean-Paul Bonnefont, Caroline Elie, Isabelle Sermet, Maryse Magen, Vincent Couloigner, M. Ferrec, Yves Manach, Bernard Lacour, Gérard Lenoir, M.N. Feuillet-Fieux
Publikováno v:
Rhinology journal. 49:347-355
The aim of this study was to address whether NP might be a predictive factor for severity of CF. The authors collected data from the literature on NP as a unique or associated sign in CF and reviewed the clinical and molecular aspects of CF associate
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bc28274100fabb57440e7d5e29b7a0da
https://doi.org/10.4193/rhino10.225
https://doi.org/10.4193/rhino10.225
Autor:
Stéphanie Bui, Thierry Bienvenu, Philippe Reix, Gabriel Bellon, Emanuelle Girodon, E. Deneuville, Isabelle Sermet-Gaudelus, Nathalie Stremmler, Albert Iron, Veronika Skalická, Michel Roussey, F. Huet, Delphine Roussel, Gérard Lenoir, M. Lebourgeois, V. Vavrova, Dorota Sands, Milan Macek, Aleksander Edelman, Jacques Sarles, Anne Munck, Isabelle Fajac
Publikováno v:
American Journal of Respiratory and Critical Care Medicine. 182:929-936
The diagnosis of cystic fibrosis (CF) is based on a characteristic clinical picture in association with a sweat chloride (Cl(-)) concentration greater than 60 mmol/L or the identification of two CF-causing mutations. A challenging problem is the sign
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::74a54144c48440c1a8fc6f8c97e6abeb
https://doi.org/10.1164/rccm.201003-0382oc
https://doi.org/10.1164/rccm.201003-0382oc
Autor:
Jean François Lesure, A. Fajac, N. Davy, Isabelle Sermet-Gaudelus, L. Bidou, Michel Renouil, S. Pierrot, Gérard Lenoir, J. P. Rousset, B. Parbaille, Elise Bismuth, Aleksander Edelman, P. Reinert
Publikováno v:
BMC Medicine, Vol 16, Iss 1, Pp 1-1 (2018)
BMC Medicine
BMC Medicine
Background Cystic fibrosis (CF) is caused by mutations in the gene encoding the cystic fibrosis transmembrane conductance regulator (CFTR) protein, which acts as a chloride channel activated by cyclic AMP (cAMP). The most frequent mutation found in 7
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7bff4a6d6892ada1afe4570138963c29
http://link.springer.com/article/10.1186/s12916-018-1138-z
http://link.springer.com/article/10.1186/s12916-018-1138-z
Publikováno v:
Journal of Innate Immunity. 2:260-266
Cystic fibrosis (CF) is a chronic inflammatory lung disease characterized by polymorphonuclear neutrophil (PMN)-dominated airway inflammation. Defective apoptosis might explain PMN persistence at these inflammation sites. We previously reported that
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e7bd309449ee4728b68438afafa59e0f
https://doi.org/10.1159/000295791
https://doi.org/10.1159/000295791
Autor:
Yann Consigny, Lucie Hertz-Pannier, Robert Girot, Gérard Lenoir, Valentine Brousse, Mariane de Montalembert, Jean-Louis Bresson, Elsa Mirre
Publikováno v:
Annals of Hematology
Annals of Hematology, Springer Verlag, 2008, 88 (8), pp.785-788. ⟨10.1007/s00277-008-0670-x⟩
Annals of Hematology, 2008, 88 (8), pp.785-788. ⟨10.1007/s00277-008-0670-x⟩
Annals of Hematology, Springer Verlag, 2008, 88 (8), pp.785-788. 〈10.1007/s00277-008-0670-x〉
Annals of Hematology, Springer Verlag, 2008, 88 (8), pp.785-788. ⟨10.1007/s00277-008-0670-x⟩
Annals of Hematology, 2008, 88 (8), pp.785-788. ⟨10.1007/s00277-008-0670-x⟩
Annals of Hematology, Springer Verlag, 2008, 88 (8), pp.785-788. 〈10.1007/s00277-008-0670-x〉
International audience; A retrospective study was conducted to assess changes in cerebrovascular lesions, as assessed by magnetic resonance (MR) imaging and angiography in 18 children with sickle cell disease (SCD) receiving optimised chronic transfu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f727c5ea442cd02473aff2c40658d71b
https://doi.org/10.1007/s00277-008-0670-x
https://doi.org/10.1007/s00277-008-0670-x
Autor:
Agnès Ferroni, S. Vrielynck, Aurélie Werkhauser-Bertrand, Gérard Lenoir, Raphaëlle Beauvais, Muriel Le Bourgeois, Isabelle Sermet-Gaudelus, Patrick Berche, Christelle Durand
Publikováno v:
Journal of Cystic Fibrosis. 7:477-482
Pathogenic bacterial colonisation in Cystic Fibrosis patients is associated with a poor prognosis; thus, protective measures need to be taken to prevent their transmission. We studied the extent of contamination in the environment of hospitalised chi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8abfe8c3dd2cabf184d0a47547464f27
https://doi.org/10.1016/j.jcf.2008.05.001
https://doi.org/10.1016/j.jcf.2008.05.001
Publikováno v:
Archives de Pédiatrie. 15:37-40
Aujourd'hui les personnes ne « savent plus manger ». Elles ont entendu tout et son contraire, elles ont perdu leurs reperes. Les consommateurs n'ont plus confiance en eux-memes, en leur capacite naturelle a s'alimenter. Ils connaissent les recomman
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::cc20b46d8daab8886a426a793972d4dd
https://doi.org/10.1016/j.arcped.2007.09.011
https://doi.org/10.1016/j.arcped.2007.09.011