Torthaí cuardaigh - Sermet‐Gaudelus, Isabelle

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

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Airway Surface Liquid pH Regulation in Airway Epithelium Current Understandings and Gaps in Knowledge de réir Zajac, Miroslaw, Dreano, Elise, Edwards, Aurelie, Planelles, Gabrielle, Sermet-Gaudelus, Isabelle

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Achromobacter xylosoxidans airway infection is associated with lung disease severity in children with cystic fibrosis de réir Marsac, Charlotte, Berdah, Laura, Thouvenin, Guillaume, Sermet-Gaudelus, Isabelle, Corvol, Harriet

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Sweat Chloride Testing and Nasal Potential Difference (NPD) Are Primary Outcome Parameters in Treatment with Cystic Fibrosis Transmembrane Conductance Regulator (CFTR) Modulators de réir Sermet-Gaudelus, Isabelle, Nguyen-Khoa, Thao, Hatton, Aurélie, Hayes, Kate, Pranke, Iwona

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Characterization of Nasal Potential Difference in cftr Knockout and F508del-CFTR Mice de réir Saussereau, Emilie Lyne, Roussel, Delphine, Diallo, Siradiou, Debarbieux, Laurent, Edelman, Aleksander, Sermet-Gaudelus, Isabelle

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Use of 16S rRNA Gene Sequencing for Identification of Nonfermenting Gram-Negative Bacilli Recovered from Patients Attending a Single Cystic Fibrosis Center de réir Ferroni, Agnes, Sermet-Gaudelus, Isabelle, Abachin, Eric, Quesne, Gilles, Lenoir, Gerard, Berche, Patrick, Gaillard, Jean-Louis

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

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Determinants of Refusal of A/H1N1 Pandemic Vaccination in a High Risk Population: A Qualitative Approach de réir d'Alessandro, Eugenie, Hubert, Dominique, Launay, Odile, Bassinet, Laurence, Lortholary, Olivier, Jaffre, Yannick, Sermet-Gaudelus, Isabelle

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A multiple reader scoring system for Nasal Potential Difference parameters de réir Solomon, George M., Liu, Bo, Sermet-Gaudelus, Isabelle, Fajac, Isabelle, Wilschanski, Michael, Vermeulen, Francois, Rowe, Steven M.

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Standardized Measurement of Nasal Membrane Transepithelial Potential Difference (NPD) de réir Solomon, George M., Bronsveld, Inez, Hayes, Kathryn, Wilschanski, Michael, Melotti, Paola, Rowe, Steven M., Sermet-Gaudelus, Isabelle

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The CF-CIRC study: a French collaborative study to assess the accuracy of Cystic Fibrosis diagnosis in neonatal screening de réir Sermet-Gaudelus, Isabelle, Roussel, Delphine, Bui, Stéphanie, Deneuville, Eric, Huet, Frédéric, Reix, Philippe, Bellon, Gabriel, Lenoir, Gérard, Edelman, Aleksander

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

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Myeloperoxidase Promoter Polymorphism −463G Is Associated With More Severe Clinical Expression of Cystic Fibrosis Pulmonary Disease de réir Reynolds, Wanda F., Sermet-Gaudelus, Isabelle, Gausson, Valérie, Feuillet, Marie-Noëlle, Bonnefont, Jean-Paul, Lenoir, Gérard, Descamps-Latscha, Béatrice, Witko-Sarsat, Véronique

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Clonal Relationship and Differentiation among Mycobacterium abscessus Isolates as Determined Using the Semiautomated Repetitive Extragenic Palindromic Sequence PCR-Based DiversiLab... de réir Mougari, Faiza, Raskine, Laurent, Ferroni, Agnes, Marcon, Estelle, Sermet-Gaudelus, Isabelle, Veziris, Nicolas, Heym, Beate, Gaillard, Jean-Louis, Nassif, Xavier, Cambau, Emmanuelle

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Matrix-Assisted Laser Desorption Ionization-Time of Flight Mass Spectrometry for Identification of Nonfermenting Gram-Negative Bacilli Isolated from Cystic Fibrosis Patients de réir Degand, Nicolas, Carbonnelle, Etienne, Dauphin, Brunhilde, Beretti, Jean-Luc, Le Bourgeois, Muriel, Sermet-Gaudelus, Isabelle, Segonds, Christine, Berche, Patrick, Nassif, Xavier, Ferroni, Agnès

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A Novel Lipidomic Strategy Reveals Plasma Phospholipid Signatures Associated with Respiratory Disease Severity in Cystic Fibrosis Patients de réir Guerrera, Ida Chiara, Astarita, Giuseppe, Jais, Jean-Philippe, Sands, Dorota, Nowakowska, Anna, Colas, Julien, Sermet-Gaudelus, Isabelle, Schuerenberg, Martin, Piomelli, Daniele, Edelman, Aleksander, Ollero, Mario

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Urinary Exosomes of Patients with Cystic Fibrosis Unravel CFTR-Related Renal Disease de réir Gauthier, Sebastien, Pranke, Iwona, Jung, Vincent, Martignetti, Loredana, Stoven, Véronique, Nguyen-Khoa, Thao, Semeraro, Michaela, Hinzpeter, Alexandre, Edelman, Aleksander, Guerrera, Ida Chiara, Sermet-Gaudelus, Isabelle

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Value of the Chlorhexidine Decontamination Method for Recovery of Nontuberculous Mycobacteria from Sputum Samples of Patients with Cystic Fibrosis de réir Ferroni, Agnès, Vu-Thien, Hoang, Lanotte, Philippe, Le Bourgeois, Muriel, Sermet-Gaudelus, Isabelle, Fauroux, Brigitte, Marchand, Sophie, Varaigne, Françoise, Berche, Patrick, Gaillard, Jean-Louis, Offredo, Catherine

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

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Insights Into Patient Variability During Ivacaftor-Lumacaftor Therapy in Cystic Fibrosis de réir Hanafin, Patrick O., Sermet-Gaudelus, Isabelle, Griese, Matthias, Kappler, Matthias, Ellemunter, Helmut, Schwarz, Carsten, Wilson, John, Tan, Marsha, Velkov, Tony, Rao, Gauri G., Schneider-Futschik, Elena K.

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