P019 Complex CFTR allele [HB1] L467F-F508del is responsible for poor clinical response to elexacaftor/tezacaftor/ivacaftor CFTRm therapy in a cystic fibrosis female with the L467F-... von Kreslová, M., Libik, M., Bittenglová, R., Sýkora, J., Macek, M.

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P324 Essential fatty acid deficiency in children and young adults with cystic fibrosis – micronutrient assessment is still an actual topic von Kreslová, M., Vecka, M., Staňková, B., Žák, A., Bittenglová, R., Schwarzová, V., Kaslová, R., Sýkora, J.

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P029 Complex CFTR allele F508del-L467F in the era of elexacaftor/tezacaftor/ivacaftor (ETI) therapy: a retrospective analysis in three Czech cases who partially respond to ETI von Kreslová, M., Libik, M., Holubová, A., Gaillyová, R., Skalická, V., Doušová, T., Bartošová, J., Bílková, A., Bittenglová, R., Macek, M.

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Age-Related Progression of Microvascular Dysfunction in Cystic Fibrosis: New Detection Ways and Clinical Outcomes von Kreslová, M., Sýkorová, A., Bittenglová, R., Schwarz, J., Pomahačová, R, Jehlička, P., Kobr, J., Trefil, L., Sýkora, J.

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P192 Cardiovascular risk in patients with cystic fibrosis: a combined diagnostic approach to the detection of endothelial dysfunction in children and adults von Kreslová, M., Sýkorová, A., Jehlička, P., Bittenglová, R., Trefil, L., Sýkora, J.

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Age-Related Progression of Microvascular Dysfunction in Cystic Fibrosis: New Detection Ways and Clinical Outcomes von Kreslová, M, Sýkorová, A, Bittenglová, R, Schwarz, J, Pomahačová, R, Jehlička, P, Kobr, J, Trefil, L, Sýkora, J

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9074 POSTER DNA Hypermethylation in Progressive Advanced Non Small Cell Lung Cancer von Pesek, M, Benesova, L, Bruha, F, Mukasnabl, P, Kopeckova, M, Bittenglova, R, Fiala, O, Krakorova, G, Sefrna, F, Minarik, M

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Twenty years of care for cystic fibrosis adults in Czech Republic von Fila, L, Sedlák, V, Binková, I, Jakubec, P, Bittenglová, R, Musil, J

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349 Twenty years of care for CF adults in Czech Republic von Fila, L, Jakubec, P, Polak, J, Bittenglova, R, Binkova, I, Musil, J

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Biomarkers of extracellular matrix turnover in patients with idiopathic pulmonary fibrosis given nintedanib (INMARK study): a randomised, placebo-controlled study von Maher, TM, Stowasser, S, Nishioka, Y, White, ES, Cottin, V, Noth, I, Selman, M, Rohr, KB, Michael, A, Ittrich, C, Diefenbach, C, Jenkins, RG, Corte, T, Glaspole, I, Holmes, M, Troy, L, Veitch, E, Bondue, B, Dahlqvist, C, Louis, R, Van Meerbeeck, J, Wuyts, W, Bittenglova, R, Kolek, V, Pauk, N, Reiterer, P, Sterclova, M, Kilpeläinen, M, Mäkitaro, R, Myllärniemi, M, Purokivi, M, Rantala, T, Couturaud, F, Israel-Biet, D, Jouneau, S, Kessler, R, Lebargy, F, Marchand-Adam, S, Bollmann, T, Günther, A, Hammerl, P, Kirschner, J, Kirsten, A-M, Kreuter, M, Neurohr, C, Prasse, A, Schönfeld, N, Wiewrodt, R, Attila, S, Balazs, M, Csanky, E, Losonczy, G, Hayashi, H, Homma, S, Inoue, Y, Kitamura, H, Nishiyama, O, Ogura, T, Okamoto, M, Saito, T, Taniguchi, H, Zaizen, Y, Filipowska, M, Jarzemska, A, Pierzchala, W, Piotrowski, W, Sladek, K, Trawinska, E, Kim, YW, Park, JS, Song, JW, Aburto, M, Castillo Villegas, D, Echave-Sustaeta, JM, Garcia Fadul, C, Herrera, S, Moises, J, Molina-Molina, M, Moreno, A, Nieto, A, Rodríguez Nieto, MJ, Rodriguez-Portal, JA, Safont, B, Sellares, J, Valenzuela, C, Adamali, H, Chaudhuri, N, Gibbons, M, Hoyles, R, Maher, T, Parfrey, H, Averill, F, Chambers, S, Ettinger, N, Giessel, G, Jones, LM, Kaye, MG, Oelberg, D, Westerman, JH, Zoz, D

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The European MultiPartner IPF registry (EMPIRE): validating long-term prognostic factors in idiopathic pulmonary fibrosis von Tran, Tanja, Šterclová, Martina, Mogulkoc, Nesrin, Lewandowska, Katarzyna, Müller, Veronika, Hájková, Marta, Kramer, Mordechai R, Jovanović, Dragana, Tekavec-Trkanjec, Jasna, Studnicka, Michael, Stoeva, Natalia, Hejduk, Karel, Dušek, Ladislav, Suissa, Samy, Vašáková, Martina

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