Zobrazeno 1 - 10
of 117
pro vyhledávání: '"Clémence Martin"'
Autor:
Quentin Cassius De Linval, Maxime Barat, Mathilde Aissaoui, Marie-Pauline Talabard, Clémence Martin, Georgia Malamut, Emma Canniff, Philippe Soyer, Marie-Pierre Revel, Guillaume Chassagnon
Publikováno v:
Insights into Imaging, Vol 15, Iss 1, Pp 1-10 (2024)
Abstract Thoracic manifestations of inflammatory bowel disease (IBD) are rare, occurring in less than 1% of patients. Unlike most other extra-intestinal manifestations, they predominate in patients with ulcerative colitis rather than in Crohn’s dis
Externí odkaz:
https://doaj.org/article/ea9878bd90f440238f28487d2ce2e52f
Publikováno v:
European Respiratory Review, Vol 33, Iss 173 (2024)
Cystic fibrosis (CF) is a genetic disease caused by variants in the gene encoding for the CF transmembrane conductance regulator (CFTR) protein, a chloride and bicarbonate channel. CFTR dysfunction results in a multiorgan disease with the main clinic
Externí odkaz:
https://doaj.org/article/e65d0abd705d4af2a19b1ed22205f43a
Autor:
Laure Alexandre-Heymann, Marie Puerto, Clémence Martin, Espérie Burnet, Helen Mosnier-Pudar, Pierre-Régis Burgel, Etienne Larger
Publikováno v:
Scientific Reports, Vol 13, Iss 1, Pp 1-8 (2023)
Abstract Cystic fibrosis related diabetes (CFRD) is observed in 20–50% of adults with cystic fibrosis (CF). Pancreas abnormalities on imaging, e.g. pancreas lipomatosis, are frequent in subjects with CF. We hypothesized that specific abnormalities
Externí odkaz:
https://doaj.org/article/8fdc17443026497589990d9a689366df
Autor:
Salma Al Kahf, Baptiste Roux, Sebastien Clerc, Mona Bassehila, A Lecomte, Elsa Moncomble, Elodie Alabadan, Nina de Montmolin, Eve Jablon, Emilie François, Gérard Friedlander, Cécile Badoual, Guy Meyer, Nicolas Roche, Clémence Martin, Benjamin Planquette
Publikováno v:
PLoS ONE, Vol 18, Iss 3, p e0278673 (2023)
ObjectivesChatbots, conversational agents that walk medical students (MS) though a clinical case, are serious games that seem to be appreciated by MS. Their impact on MS's performance in exams however was not yet evaluated. Chatprogress is a chatbot-
Externí odkaz:
https://doaj.org/article/ce7b591536ca4c8590209a7a36dc3605
Autor:
Clémence Martin, Théo Dhôte, Maha Zohra Ladjemi, Muriel Andrieu, Souganya Many, Vaarany Karunanithy, Frédéric Pène, Jennifer Da Silva, Pierre-Régis Burgel, Véronique Witko-Sarsat
Publikováno v:
Frontiers in Immunology, Vol 13 (2022)
The progressive lung destruction in cystic fibrosis (CF) is tightly associated with chronic bacterial infection and neutrophil-dominated airway inflammation. CF pulmonary disease is complicated by episodes of acute exacerbations, contributing to irre
Externí odkaz:
https://doaj.org/article/0e6b7c0247c246a58d779a42880c6c6a
Autor:
Olivier Peyrony, Alice Hutin, Jennifer Truchot, Raphaël Borie, David Calvet, Adrien Albaladejo, Yousrah Baadj, Pierre-Emmanuel Cailleaux, Martin Flamant, Clémence Martin, Jonathan Messika, Alexandre Meunier, Mariana Mirabel, Victoria Tea, Xavier Treton, Sylvie Chevret, David Lebeaux, Damien Roux
Publikováno v:
BMC Medical Education, Vol 20, Iss 1, Pp 1-8 (2020)
Abstract Background The evaluation process of French medical students will evolve in the next few years in order to improve assessment validity. Script concordance testing (SCT) offers the possibility to assess medical knowledge alongside clinical re
Externí odkaz:
https://doaj.org/article/6a0ba33270d74e7ca45dcb5fc987833f
Publikováno v:
Cells, Vol 11, Iss 11, p 1769 (2022)
Cystic fibrosis (CF) is a rare genetic multisystemic disease, the manifestations of which are due to mutations in the gene encoding the CF transmembrane conductance regulator (CFTR) protein and can lead to respiratory insufficiency and premature deat
Externí odkaz:
https://doaj.org/article/b5aea729420747dea37af86587c64a87
Autor:
Amandine M. Collin, Marylène Lecocq, Sabrina Noel, Bruno Detry, François M. Carlier, Frank Aboubakar Nana, Caroline Bouzin, Teresinha Leal, Marjorie Vermeersch, Virginia De Rose, Lucile Regard, Clémence Martin, Pierre-Régis Burgel, Delphine Hoton, Stijn Verleden, Antoine Froidure, Charles Pilette, Sophie Gohy
Publikováno v:
EBioMedicine, Vol 60, Iss , Pp 102974- (2020)
Background: In cystic fibrosis (CF), recurrent infections suggest impaired mucosal immunity but whether production of secretory immunoglobulin A (S-IgA) is impaired remains elusive. S-IgA is generated following polymeric immunoglobulin receptor (pIgR
Externí odkaz:
https://doaj.org/article/06b07803ab7e44948551ce1de9ddf19f
Autor:
Clémence Martin, Pierre-Régis Burgel, Patricia Lepage, Claire Andréjak, Jacques de Blic, Arnaud Bourdin, Jacques Brouard, Pascal Chanez, Jean-Charles Dalphin, Gaetan Deslée, Antoine Deschildre, Philippe Gosset, Lhousseine Touqui, Daniel Dusser
Publikováno v:
European Respiratory Review, Vol 24, Iss 135, Pp 78-91 (2015)
This article is the summary of a workshop, which took place in November 2013, on the roles of microorganisms in chronic respiratory diseases. Until recently, it was assumed that lower airways were sterile in healthy individuals. However, it has long
Externí odkaz:
https://doaj.org/article/36e04e55a54940fd87df0f3f9cf14aab
Autor:
Léa Okroglic, Pierre Sohier, Clémence Martin, Coralie Lheure, Nathalie Franck, Isabelle Honoré, Reem Kanaan, Pierre-Régis Burgel, Agnès Carlotti, Nicolas Dupin, Bénédicte Oulès
Publikováno v:
JAMA dermatology.
ImportanceA new treatment for cystic fibrosis combining 3 CFTR modulators—elexacaftor (ELX), tezacaftor (TEZ), and ivacaftor (IVA)—has recently been approved for cystic fibrosis treatment. The cutaneous adverse effects following treatment with th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::37143e69e2267f3423db9a00c6565575
https://pubmed.ncbi.nlm.nih.gov/36449298
https://pubmed.ncbi.nlm.nih.gov/36449298