P012 Advancing precision in cystic fibrosis registries: identification and classification of patients with unclear diagnosis in the Norwegian cystic fibrosis patient registry by Wathne, A.C., Os, A., Kolsgaard, M.P., Finstad, P.L., Bakkeheim, E.

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WS4.4 Multicenter prevalence study of nontuberculous mycobacteria in patients with cystic fibrosis in Scandinavia by Qvist, T, Jönsson, B, Gilljam, M, Svahn, A, Jensen-Fangel, S, Kötz, K, Wang, M, Hansson, L, Krjukova, J, Hollsing, A, Finstad, P.L, Laerum, B.N, Høiby, N, Pressler, T, Katzenstein, T.L

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P388 Mental health scores in adults with cystic fibrosis are not strongly associated with clinical outcomes by Heddan, M.V., Christensen, B., Wathne, A.C.S., Finstad, P.L., Bakkeheim, E., Kolsgaard, M.L.P.

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P061 Low FEV1 performance in the 30–34 years of age cohort in Norway: utilising Registry data in the search for causes by Os, A., Alderslyst, H., Grøterud, B. Akselsen, Finstad, P.L., Bakkeheim, E.

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MON-LB680: Nutritional Status in Adults with Cystic Fibrosis and Pancreatic Insufficiency by Sripalan, N., Moen, I.E., Finstad, P.L., Brekke, H.K., Ekornes, M., Gharagozlian, S.

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228 Informing the children: a challenging task for the CF patient by Homme, I, Finstád, P.L, Legáárd, M

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