Výsledky vyhledávání - "MESH: Cystic Fibrosis / complications"

Lung transplantation for cystic fibrosis and bronchiectasis

Autor: Renaud-Picard, B., Tissot, A., Burgel, P.R., Grenet, D., de Miranda, S., Coiffard, B.

Publikováno v: Revue des Maladies Respiratoires
Revue des Maladies Respiratoires, 2023, 40, pp.e33-e41. ⟨10.1016/j.rmr.2022.12.011⟩

International audience; No abstract available

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=od______3430::53e589a197c448e1691e65772bb0d4dc
https://www.hal.inserm.fr/inserm-04061234

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Aspergillus Sensitization or Carriage in Cystic Fibrosis Patients

Autor: Jean-François Magnaval, Christine Segonds, M. Murris, Sophie Cassaing, F. Brémont, Laurent Tétu, Bernard Pipy, Judith Fillaux

Publikováno v: Pediatric Infectious Disease Journal
Pediatric Infectious Disease Journal, Lippincott, Williams & Wilkins, 2014, 33 (7), pp.680-686. ⟨10.1097/INF.0000000000000231⟩
Pediatric Infectious Disease Journal, 2014, 33 (7), pp.680-686. ⟨10.1097/INF.0000000000000231⟩

International audience; Background: Aspergillus fumigatus (Af) sensitization and persistent carriage are deleterious to lung function, but no consensus has been reached defining these medical entities. This work aimed to identify possible predictive

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::af53f93b04130e2e5fad29d6eed4da4c
https://hal-univ-tlse3.archives-ouvertes.fr/hal-03279246

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Prospective Multicenter Study of Pneumocystis jirovecii Colonization among Cystic Fibrosis Patients in France

Autor: Julia Salleron, Emilie Fréalle, Benoit Wallaert, Francisca Hernández-Hernández, Patrick Caneiro, Eduardo Dei-Cas, Isabelle Accoceberry, Laurence Delhaes, Jean-Philippe Bouchara, Isabelle Durand-Joly

Publikováno v: Journal of Clinical Microbiology
Journal of Clinical Microbiology, 2012, 50 (12), pp.4107-4110. ⟨10.1128/JCM.01974-12⟩
Journal of Clinical Microbiology, American Society for Microbiology, 2012, 50 (12), pp.4107-4110. ⟨10.1128/JCM.01974-12⟩

Pneumocystis carriage was detected in 12.5% of 104 cystic fibrosis (CF) patients during a prospective multicenter French study, with a prevalence of genotype 85C/248C and geographic variations. It was significantly associated with the absence of Pseu

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::539d6688f57b98a4ce8bdcdabcbf629d
https://univ-angers.hal.science/hal-03134628

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Reverse line blot hybridisation screening of Pseudallescheria/Scedosporium species in patients with cystic fibrosis

Autor: Q, Lu, A H G Gerrits, van den Ende, G S, de Hoog, R, Li, I, Accoceberry, I, Durand-Joly, J-P, Bouchara, F, Hernandez, L, Delhaes

Publikováno v: Mycoses
Mycoses, 2011, 54 (Suppl. 3), pp.5-11. ⟨10.1111/j.1439-0507.2011.02108.x⟩
Mycoses, 54, 5-11. John Wiley and Sons Ltd
Mycoses, 54(suppl. s3), 5-11. Wiley-Blackwell

International audience; The PCR-RLB (reverse line blot hybridisation) was applied as a molecular technique for the detection of members of Pseudallescheria and Scedosporium from sputum of patients with cystic fibrosis (CF). Fifty-nine sputum samples

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::3c305fab35083275e9227cdc99652723
https://univ-angers.hal.science/hal-03134645

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Fungal respiratory infections in cystic fibrosis: a growing problem

Autor: Françoise Symoens, Jean-Philippe Bouchara, R. Horré, Laurence Delhaes

Publikováno v: Medical Mycology
Medical Mycology, Oxford University Press, 2010, 48 (Suppl. 1), pp.S1-S3. ⟨10.3109/13693786.2010.529304⟩
Medical Mycology, 2010, 48 (Suppl. 1), pp.S1-S3. ⟨10.3109/13693786.2010.529304⟩

tions increases as the life expectancy of patients improves. But in contrast to bacterial respiratory infections, relatively little progress has been made with regards to fungal respiratory infections. Aspergillus fumigatus is by far the most common

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9ab11f07371e82ffcf70bc181e47df43
https://hal.univ-angers.fr/hal-03137656

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Occurrence and relevance of filamentous fungi in respiratory secretions of patients with cystic fibrosis — a review

Autor: Marc Pihet, Jacqueline Carrere, Bernard Cimon, Dominique Chabasse, Laurence Delhaes, Françoise Symoens, Jean-Philippe Bouchara

Publikováno v: Medical Mycology
Medical Mycology, 2009, 47 (4), pp.387-397. ⟨10.1080/13693780802609604⟩

International audience; The colonization of airways by filamentous fungi and the development of respiratory infections require some predisposing factors as encountered in patients with cystic fibrosis (CF). Indeed, the defective mucociliary clearance

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::39fd1edd2266c21bc59953418da3df57
https://hal.univ-angers.fr/hal-03134656

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High resolution genotyping of Aspergillus fumigatus isolates recovered from chronically colonised patients with cystic fibrosis

Autor: Lies M. E. Vanhee, Jean-Philippe Bouchara, Françoise Symoens, Tom Coenye, Hans Nelis

Publikováno v: EUROPEAN JOURNAL OF CLINICAL MICROBIOLOGY & INFECTIOUS DISEASES
European Journal of Clinical Microbiology & Infectious Diseases: Official Publication of the European Society of Clinical Microbiology
European Journal of Clinical Microbiology & Infectious Diseases: Official Publication of the European Society of Clinical Microbiology, 2008, 27 (10), pp.1005-1007. ⟨10.1007/s10096-008-0527-1⟩

International audience; A series of 256 Aspergillus fumigatus isolates, recovered from eight patients with cystic fibrosis (CF), were genotyped using microsatellite-based typing. Only a limited number of genotypes were shared between patients and co-

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::72b97defa34f69eb5cc8017521306531
https://biblio.ugent.be/publication/481100

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