Výsledky vyhledávání - "S, Vrielynck"

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Evolution of sinonasal clinical features in children with cystic fibrosis

Autor: Ruben Hermann, Eric Truy, P. Suy, S Ayari-Khalfallah, S. Vrielynck, A. Coudert

Publikováno v: International Journal of Pediatric Otorhinolaryngology
International Journal of Pediatric Otorhinolaryngology, Elsevier, 2019, 124, pp.47-53. ⟨10.1016/j.ijporl.2019.05.030⟩

International audience; Objective: to assess the evolution of sinonasal manifestations in children with cystic fibrosis, since the improvement of their prognosis over the last decades.Methods: an observational, monocentric study with a retrospective

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6a999e2f5a1054b03f951b873fd7d764
https://doi.org/10.1016/j.ijporl.2019.05.030

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An impulse oscillometry system is less efficient than spirometry in tracking lung function improvements after intravenous antibiotic therapy in pediatric patients with cystic fibrosis

Autor: Clélia Buchs, Philippe Reix, S. Vrielynck, Laurianne Coutier, V. Jubin, Catherine Mainguy

Publikováno v: Pediatric Pulmonology. 50:1073-1081

A literature search identified one retrospective study on the responsiveness of impulse oscillometry (IOS) in pediatric patients with cystic fibrosis. The aim of this prospective observational study was to assess this property in an adequately powere

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::5d811368c3aa45ed48baa1df1aa138a8
https://doi.org/10.1002/ppul.23301

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Guidelines for the clinical management and follow-up of infants with inconclusive cystic fibrosis diagnosis through newborn screening

Autor: E. Deneuville, M.-P. Audrézet, J. Brouard, N. Wizla, N. Remus, L. Couderc Kohen, Emmanuelle Girodon, S. Vrielynck, K. LLerena, C. Raynal, Laurence Weiss, Thao Nguyen-Khoa, Isabelle Sermet-Gaudelus, M. Le Bourgeois, Michel Roussey

Publikováno v: Archives de Pédiatrie
Archives de Pédiatrie, Elsevier, 2017, 24 (12), pp.e1-e14. ⟨10.1016/j.arcped.2017.07.015⟩

Summary Neonatal screening for cystic fibrosis (CF) can detect infants with elevated immunoreactive trypsinogen (IRT) levels and inconclusive sweat tests and/or CFTR DNA results. These cases of uncertain diagnosis are defined by (1) either the presen

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::447df127566203389d884e1cb3b97338
https://hal-normandie-univ.archives-ouvertes.fr/hal-02272269

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164 Are viral respiratory infections a real issue in infants with cystic fibrosis: preliminary results of a prospective cohort study

Autor: Philippe Reix, S. Vrielynck, M. Perceval, F. Morfin, V. Jubin, Anne Doléans-Jordheim, M. Eymery

Publikováno v: Journal of Cystic Fibrosis
Journal of Cystic Fibrosis, Elsevier, 2017, Abstracts of the 40th European Cystic Fibrosis Conference, 16, Supplement 1, pp.S108. ⟨10.1016/S1569-1993(17)30528-3⟩

International audience

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5dc24380e4368352f66b3ca8830f1e0e
https://hal-univ-lyon1.archives-ouvertes.fr/hal-02487209

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Recommandations nationales pour la prise en charge du nourrisson dépisté atteint de mucoviscidose. Consensus de la fédération des centres de ressources et de compétences de la mucoviscidose

Autor: Michel Roussey, M.-L. Dalphin, Anne Munck, L. Weiss, C. Llerena, Jacques Brouard, A. Dirou, Laure Couderc, G. Rault, C. Bailly, M. Lebourgeois, N. Wizla, M. Renouil, Isabelle Sermet-Gaudelus, S. Vrielynck

Publikováno v: Archives de Pédiatrie. 21:654-662

Resume Ces recommandations sont destinees a harmoniser les procedures concernant la prise en charge des nourrissons de moins de 2 ans atteints de formes typiques de mucoviscidose et diagnostiques par depistage neonatal. Elles ont ete elaborees par le

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::85df8b00be4090185a21e5a4c49ff4c9
https://doi.org/10.1016/j.arcped.2014.03.014

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[Management of infants whose diagnosis is inconclusive at neonatal screening for cystic fibrosis]

Autor: I, Sermet-Gaudelus, J, Brouard, M-P, Audrézet, L, Couderc Kohen, L, Weiss, N, Wizla, S, Vrielynck, K, LLerena, M, Le Bourgeois, E, Deneuville, N, Remus, T, Nguyen-Khoa, C, Raynal, M, Roussey, E, Girodon

Publikováno v: Archives de pediatrie : organe officiel de la Societe francaise de pediatrie. 24(4)

Neonatal screening for cystic fibrosis (CF) may detect infants with elevated immunoreactive trypsinogen (IRT) levels but with inconclusive sweat tests and/or DNA results. This includes cases associating (1) either the presence of at most one CF-causi

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::7f05973fbc932cdad1ab3efbb73a47f3
https://pubmed.ncbi.nlm.nih.gov/28258861

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