Long-term evaluation of respiratory status after esophageal atresia repair von Beucher, J., Wagnon, J., Daniel, V., Habonimana, E., Fremond, B., Lapostolle, C., Guillot, S., Azzis, O., Dabadie, A., Deneuville, E.

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Guidelines for the clinical management and follow-up of infants with inconclusive cystic fibrosis diagnosis through newborn screening von Sermet-Gaudelus, I., Brouard, J., Audrézet, M.-P., Couderc Kohen, L., Weiss, L., Wizla, N., Vrielynck, S., LLerena, K., Le Bourgeois, M., Deneuville, E., Remus, N., Nguyen-Khoa, T., Raynal, C., Roussey, M., Girodon, E.

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Characteristics of endobronchial primitive tumors in children von Eyssartier, E., Ang, P., Bonnemaison, E., Gibertini, I., Diot, P., Carpentier, E., Chantepie, A., Leclair, M.D., Brouard, J., Boutard, P., Deneuville, E., Marie-Cardine, A., Lardy, H.

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220 Does cystic fibrosis have an impact on school absenteeism? von Vigier, C, Lefeuvre, S, Dabadie, A, Beucher, J, Dagorne, M, Rault, G, Storni, V, Vigneron, P, Pladys, P, Deneuville, E

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Respiratory outcome of bronchopulmonary dysplasia in school-age children von Kathegesu, E, Beucher, J, Daniel, V, Guillot, S, Lefeuvre, S, Deneuville, E, Pladys, P

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159 Pneumocystis jirovecii and cystic fibrosis in Britanny, France von Le Gal, S, Robert-Gangneux, F, Damiani, C, Virmaux, M, Belleguic, C, Deneuville, E, Rault, G, Ramel, S, Bihan, J.L, Guillaud-Saumur, T, Pougnet, L, Totet, A, Gangneux, J.-P, Bouchara, J.-P, Nevez, G

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Indoor fungal exposure: What impact on clinical and biological status regarding Aspergillus during cystic fibrosis von Pricope, D, Deneuville, E, Frain, S, Chevrier, S, Belaz, S, Roussey, M, Gangneux, J-P

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Management of infants whose diagnosis is inconclusive at neonatal screening for cystic fibrosis von Sermet-Gaudelus, I, Brouard, J, Audrézet, M-P, Couderc Kohen, L, Weiss, L, Wizla, N, Vrielynck, S, LLerena, K, Le Bourgeois, M, Deneuville, E, Remus, N, Nguyen-Khoa, T, Raynal, C, Roussey, M, Girodon, E

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40 Is oxidative stress responsible for plasma membrane integrity alteration in macrophages from patients with cystic fibrosis? von Le Trionnaire, S, Lévêque, M, Belleguic, C, Deneuville, E, Desrues, B, Brinchault, G, Dabadie, A, Roussey, M, Jouneau, S, Gangneux, J.-P, Dimanche-Boitrel, M.-T, Martin-Chouly, C

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Neonatal screening of cystic fibrosis: diagnostic problems with CFTR mild mutations von Roussey, M., Le Bihannic, A., Scotet, V., Audrezet, M. P., Blayau, M., Dagorne, M., David, V., Deneuville, E., Giniès, J. L., Laurans, M., Moisan‐Petit, V., Rault, G., Vigneron, P., Férec, C.

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Primary ciliary dyskinesia: medical practice in Rennes von Deneuville, E, Beucher, J, Chambellan, A, Beloncle, C, Kathegesu, E, Segalen, J

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P102 Clear illustration of improved survival in cystic fibrosis using the Kaplan-Meier method: the 50-year experience of Brittany, France von L’Hostis, C., Derrien, J., Audrézet, M.-P., Ramel, S., Belleguic, C., Deneuville, E., Storni, V., Munck, M.-R., Frachon, I., Vic, P., Bernard, R., Férec, C., Scotet, V.

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EPS6.02 Striking evolution of survival of cystic fibrosis patients in Brittany (western France): an analysis of the last 50 years by birth cohort von Derrien, J., L’Hostis, C., Audrézet, M.-P., Ramel, S., Belleguic, C., Deneuville, E., Arnouat, B., Storni, V., Munck, M.-R., Frachon, I., Vic, P., Bernard, R., Férec, C., Scotet, V.

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Review of respiratory impact in oesophageal atresia von Deneuville, E, Beucher, J, Wagnon, J, Lapostolle, C, Guillot, S, Hesse, N, Habonimana, E, Azzis, O, Fremont, B, Dabadie, A

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504 Elexacaftor/tezacaftor/ivacaftor population pharmacokinetics in children with CF von Truong, N., Benaboud, S., Bardin, E., Miralles, M., Lui, G., Froelicher-Bournaud, L., Rouillon, S., Bouazza, N., Stremler, N., Bihouee, T., Bessaci-Kabouya, K., Deneuville, E., Laurans, M., Reix, P., Mittaine, M., Bui, S., Weiss, L., Barboura, M., Bonnel, A., Treluyer, J., Sermet-Gaudelus, I., Foissac, F.

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WS15.03 Elexacaftor/tezacaftor/ivacaftor population pharmacokinetics in paediatric patients with cystic fibrosis von Truong, N.H., Benaboud, S., Bardin, E., Miralles, M., Lui, G., Froelicher-Bournaud, L., Rouillon, S., Bouazza, N., Stremler, N., Bihouee, T., Bessaci-Kabouya, K., Coirier-Duet, E., Marguet, C., Deneuville, E., Laurans, M., Reix, P., Gerardin, M., Mittaine, M., Epaud, R., Thumerelle, C., Weiss, L., Treluyer, J.-M., Sermet-Gaudelus, I., Foissac, F.

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689 Triple CFTR modulator combination improves glucose tolerance in adolescents with cystic fibrosis: data from the French observational pediatric study MODUL-CF von Weiss, L., Galderisi, A., Besançon, A., Stremler, N., Reix, P., Wizla, N., Rames, C., Marguet, C., Tatapoulos, A., Perrisson, C., Dalphin, M., Troussier, F., Houdouin, V., Abely, M., Cosson, L., Gabsi, A., Corvol, H., Deneuville, E., Sahki, D., Bonnel, A., Group, M., Sermet-Gaudelus, I.

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P286 Triple CFTR modulator combination improves glucose tolerance in adolescents with cystic fibrosis. Data from the French observational paediatric study MODUL-CF von Weiss, L., Galderisi, A., Besançon, A., Stremler, N., Reix, P., Wizla, N., Rames, C., Marguet, C., Tatapoulos, A., Perrisson, C., Dalphin, M.-L., Troussier, F., Houdouin, V., Abely, M., Cosson, L., Gabsi, A., Corvol, H., Deneuville, E., Storni, V., Ramel, S., Bui, S., Heraud, M.-C., Epaud, R., Huet, F., Scalbert, M., Mely, L., Gachelin, E., Giannantonio, M., Sahki, D., Lustre, A., Bonnel, A.-S., Sermet, I.

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P003 The diffusion processes of the CFTR mutations in Brittany (France) von Pellen, N., Bellis, G., Rault, G., Gueganton, L., Belleguic, C., Deneuville, E., Journel, H., Ramel, S., Scotet, V., Ferec, C.

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149 2009 H1N1 influenza A in cystic fibrosis patients. A French collaborative study von Bucher, J, Hubert, D, Bellon, G, Deneuville, E, Delaisi, B, Corvol, H, Boussaud, V, Bremont, F, Ramadour, M, Petit, I, Renouil, M, Vodoff, M.V, Troussier, F, Vallier, C, Remus, N, Bassinet, L, Grenet, D, Leruez, M, Launay, O, Lortholary, O, Sermet-Gaudelus, L

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