Search Results - Isabelle Sermet‐Gaudelus

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  1. 1
    Ivacaftor treatment in patients with cystic fibrosis and the G551D-CFTR mutation

    Ivacaftor treatment in patients with cystic fibrosis and the G551D-CFTR mutation by Isabelle Sermet‐Gaudelus

    Published 2013
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  2. 2
    Therapeutic Approaches for Patients with Cystic Fibrosis Not Eligible for Current CFTR Modulators

    Therapeutic Approaches for Patients with Cystic Fibrosis Not Eligible for Current CFTR Modulators by Isabelle Fajac, Isabelle Sermet‐Gaudelus

    Published 2021
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  3. 3
    Guidelines on the early management of infants diagnosed with cystic fibrosis following newborn screening

    Guidelines on the early management of infants diagnosed with cystic fibrosis following newborn screening by Isabelle Sermet‐Gaudelus, Sarah Mayell, Kevin W Southern

    Published 2010
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  4. 4
    Bone demineralization is improved by ivacaftor in patients with cystic fibrosis carrying the p.Gly551Asp mutation

    Bone demineralization is improved by ivacaftor in patients with cystic fibrosis carrying the p.Gly551Asp mutation by Isabelle Sermet‐Gaudelus, M. Delion, I. Durieu, Jacky Jacquot, D. Hubert

    Published 2016
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  5. 5
    Emerging Therapeutic Approaches for Cystic Fibrosis. From Gene Editing to Personalized Medicine

    Emerging Therapeutic Approaches for Cystic Fibrosis. From Gene Editing to Personalized Medicine by Iwona Pranke, Anita Golec, Alexandre Hinzpeter, Aleksander Edelman, Isabelle Sermet‐Gaudelus

    Published 2019
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  6. 6
    Airway Surface Liquid pH Regulation in Airway Epithelium Current Understandings and Gaps in Knowledge

    Airway Surface Liquid pH Regulation in Airway Epithelium Current Understandings and Gaps in Knowledge by Mirosław Zając, Elise Dréano, Aurélie Edwards, Gabrielle Planelles, Isabelle Sermet‐Gaudelus

    Published 2021
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  7. 7
    Cystic fibrosis bone disease treatment: Current knowledge and future directions

    Cystic fibrosis bone disease treatment: Current knowledge and future directions by Melissa S. Putman, Abeer Anabtawi, Trang N. Le, Vin Tangpricha, Isabelle Sermet‐Gaudelus

    Published 2019
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  8. 8
    Cystic fibrosis in Europe: improved lung function and longevity – reasons for cautious optimism, but challenges remain

    Cystic fibrosis in Europe: improved lung function and longevity – reasons for cautious optimism, but challenges remain by Eitan Kerem, Annalisa Orenti, Arianna Adamoli, Elpis Hatziagorou, Lutz Naehrlich, Isabelle Sermet‐Gaudelus

    Published 2024
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  9. 9
    Plasma lipidomics reveals potential prognostic signatures within a cohort of cystic fibrosis patients

    Plasma lipidomics reveals potential prognostic signatures within a cohort of cystic fibrosis patients by Mario Ollero, Giuseppe Astarita, Ida Chiara Guerrera, Isabelle Sermet‐Gaudelus, Stéphanie Trudel, Daniele Piomelli, Aleksander Edelman

    Published 2011
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  10. 10
    ECFS standards of care on CFTR-related disorders: Updated diagnostic criteria

    ECFS standards of care on CFTR-related disorders: Updated diagnostic criteria by Carlo Castellani, K. De Boeck, Elke De Wachter, Isabelle Sermet‐Gaudelus, N.J. Simmonds, K.W. Southern

    Published 2022
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  11. 11
    Simple pediatric nutritional risk score to identify children at risk of malnutrition

    Simple pediatric nutritional risk score to identify children at risk of malnutrition by Isabelle Sermet‐Gaudelus, Anne-Sylvie Poisson-Salomon, V. Colomb, M.C. Brusset, Françoise Mosser, Fabienne Berrier, C. Ricour

    Published 2000
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  12. 12
    A European consensus for the evaluation and management of infants with an equivocal diagnosis following newborn screening for cystic fibrosis

    A European consensus for the evaluation and management of infants with an equivocal diagnosis following newborn screening for cystic fibrosis by Sarah Mayell, À. Munck, J.V. Craig, Isabelle Sermet‐Gaudelus, K. Brownlee, Martin Schwarz, Carlo Castellani, Kevin W Southern

    Published 2008
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  13. 13
    Impact of COVID-19 on people with cystic fibrosis

    Impact of COVID-19 on people with cystic fibrosis by Carla Colombo, Pierre‐Régis Burgel, Silvia Gärtner, Silke van Koningsbruggen‐Rietschel, Lutz Naehrlich, Isabelle Sermet‐Gaudelus, Kevin W Southern

    Published 2020
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  14. 14
    Cystic fibrosis transmembrane conductance regulator (CFTR) regulates the production of osteoprotegerin (OPG) and prostaglandin (PG) E2 in human bone

    Cystic fibrosis transmembrane conductance regulator (CFTR) regulates the production of osteoprotegerin (OPG) and prostaglandin (PG) E2 in human bone by Louis Le Heron, Christine Guillaume, Frédéric Velard, Julien Braux, Lhousseine Touqui, Sandra Moriceau, Isabelle Sermet‐Gaudelus, D. Laurent‐Maquin, Jacky Jacquot

    Published 2009
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  15. 15
    Follow-up of 452 totally implantable vascular devices in cystic fibrosis patients

    Follow-up of 452 totally implantable vascular devices in cystic fibrosis patients by À. Munck, S. Malbezin, J. Bloch, M. Gérardin, Muriel Lebourgeois, J. Derelle, F. Brémont, Isabelle Sermet‐Gaudelus, M.-R. Munck, J Navarro

    Published 2004
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  16. 16
    Matrix-Assisted Laser Desorption Ionization-Time of Flight Mass Spectrometry for Identification of Nonfermenting Gram-Negative Bacilli Isolated from Cystic Fibrosis Patients

    Matrix-Assisted Laser Desorption Ionization-Time of Flight Mass Spectrometry for Identification of Nonfermenting Gram-Negative Bacilli Isolated from Cystic Fibrosis Patients by Nicolas Degand, Étienne Carbonnelle, Brunhilde Dauphin, Jean‐Luc Béretti, M. Le Bourgeois, Isabelle Sermet‐Gaudelus, Christine Segonds, Patrick Berche, Xavier Nassif, Agnès Ferroni

    Published 2008
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  17. 17
    Association between Staphylococcus aureus alone or combined with Pseudomonas aeruginosa and the clinical condition of patients with cystic fibrosis

    Association between Staphylococcus aureus alone or combined with Pseudomonas aeruginosa and the clinical condition of patients with cystic fibrosis by D. Hubert, Hélène Réglier‐Poupet, Isabelle Sermet‐Gaudelus, Agnès Ferroni, M. Le Bourgeois, Pierre‐Régis Burgel, Raphaël Serreau, Daniel Dusser, Claire Poyart, Joël Coste

    Published 2013
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  18. 18
    Moving the Dial on Airway Inflammation in Response to Trikafta in Adolescents with Cystic Fibrosis

    Moving the Dial on Airway Inflammation in Response to Trikafta in Adolescents with Cystic Fibrosis by Agathe Lepissier, Anne Sophie Bonnel, Nathalie Wizla, Laurence Weiss, Marie Mittaine, Katia Bessaci, Eitan Kerem, Véronique Houdouin, Philippe Reix, Christophe Marguet, Isabelle Sermet‐Gaudelus

    Published 2023
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  19. 19
    <i>Pseudomonas aeruginosa</i>LasB protease impairs innate immunity in mice and humans by targeting a lung epithelial cystic fibrosis transmembrane regulator–IL-6–antimicrobial–repair pathway

    <i>Pseudomonas aeruginosa</i>LasB protease impairs innate immunity in mice and humans by targeting a lung epithelial cystic fibrosis transmembrane regulator–IL-6–antimicrobial–repa... by Vinciane Saint‐Criq, Bérengère Villeret, Fabien Bastaert, Saadé Kheir, Aurélie Hatton, Aurélie Cazes, Zhou Xing, Isabelle Sermet‐Gaudelus, Ignacio García-Verdugo, Aleksander Edelman, Jean‐Michel Sallenave

    Published 2017
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  20. 20
    Modulators of CFTR. Updates on clinical development and future directions

    Modulators of CFTR. Updates on clinical development and future directions by Emmanuelle Bardin, Alexandra Pastor, Michaëla Semeraro, Anita Golec, Kate Hayes, B. Chevalier, Farouk Berhal, Guillaume Prestat, Alexandre Hinzpeter, Christine Gravier‐Pelletier, Iwona Pranke, Isabelle Sermet‐Gaudelus

    Published 2021
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