Multiple-breath inert gas washout and spirometry versus structural lung disease in cystic fibrosis von Gustafsson, P M, De Jong, P A, Tiddens, H A W M, Lindblad, A

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Improved treatment response to dornase alfa in cystic fibrosis patients using controlled inhalation von BAKKER, E. M, VOLPI, S, SALONINI, E, VAN DER WIEL-KOOIJ, E. C, SINTNICOLAAS, C. J. J. C. M, HOP, W. C. J, ASSAEL, B. M, MERKUS, P. J. F. M, TIDDENS, H. A. W. M

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Lung parenchyma and structure visualisation in paediatric chest MRI: a comparison of different short and ultra-short echo time protocols von Papp, D., Elders, B., Wielopolski, P.A., Kotek, G., Vogel, M., Tiddens, H.A.W.M., Ciet, P., Hernandez-Tamames, J.A.

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Introduction of Ivacaftor/Lumacaftor in Children With Cystic Fibrosis Homozygous for F508del in the Netherlands: A Nationwide Real-Life Study von Zwitserloot, A M, Aziz, S Z, Chen, Y, Bannier, M A G E, Janssens, H M, Merkus, P F J M, Nuijsink, M, Terheggen-Lagro, S W J, Tiddens, H A W M, Zomer-van Ommen, D D, Vonk, J M, de Winter-de Groot, K M, Willemse, B W M, Koppelman, G H

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Model of mucociliary clearance in cystic fibrosis lungs von Kurbatova, P., Bessonov, N., Volpert, V., Tiddens, H.A.W.M., Cornu, C., Nony, P., Caudri, D.

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Open label study of inhaled aztreonam for Pseudomonas eradication in children with cystic fibrosis: The ALPINE study von Tiddens, H.A.W.M, De Boeck, K, Clancy, J.P, Fayon, M, H.G.M., Arets, Bresnik, M, Derchak, A, Lewis, S.A, Oermann, C.M

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Progressive damage on high resolution computed tomography despite stable lung function in cystic fibrosis von de Jong, P.A, Nakano, Y, Lequin, M.H, Mayo, J.R, Woods, R, Pare, P.D, Tiddens, H.A.W.M

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Progression of lung disease on computed tomography and pulmonary function tests in children and adults with cystic fibrosis von de Jong, P A, Lindblad, A, Rubin, L, Hop, W C J, de Jongste, J C, Brink, M, Tiddens, H A W M

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Imaging of respiratory muscles in neuromuscular disease: A review von Harlaar, L., Ciet, P., van der Ploeg, A.T., Brusse, E., van der Beek, N.A.M.E., Wielopolski, P.A., de Bruijne, M., Tiddens, H.A.W.M., van Doorn, P.A.

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Recombinant human DNase nebulisation in children with cystic fibrosis: before bedtime or after waking up? von van der Giessen, L. J, Gosselink, R, Hop, W. C. J, Tiddens, H. A. W. M

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Pharmacokinetics of inhaled monodisperse beclomethasone as a function of particle size von Esposito‐Festen, J. E., Zanen, P., Tiddens, H. A. W. M., Lammers, J.‐W. J.

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Pharmacokinetics and Tolerability of Once Daily Double Dose Tobramycin Inhalation in Cystic Fibrosis Using Controlled and Conventional Nebulization von van Velzen, A J, Bos, A C, Touw, D J, Tiddens, H A W M, Heijerman, H G M, Janssens, H M

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Small airway deposition of dornase alfa during exacerbations in cystic fibrosis; a randomized controlled clinical trial von Bakker, E.M., Volpi, S., Salonini, E., Müllinger, B., Kroneberg, P., Bakker, M., Hop, W.C.J., Assael, B.M., Tiddens, H.A.W.M.

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Development of a core outcome set for congenital pulmonary airway malformations: study protocol of an international Delphi survey von Hermelijn, Sergei, Kersten, Casper, Mullassery, Dhanya, Muthialu, Nagarajan, Cobanoglu, Nazan, Gartner, Silvia, Bagolan, Pietro, Mesas Burgos, Carmen, Sgro, Alberto, Heyman, Stijn, Till, Holger, Suominen, Janne, Schurink, Maarten, Desender, Liesbeth, Losty, Paul, Ertresvag, Kjetil, Tiddens, Harm A W M, Wijnen, Rene M H, Schnater, Marco, Hermelijn, S.M., Kersten, C.M., Schnater, J.M., Wijnen, R.M.H., Tiddens, H.A.W.M., Cochius, S.C.M., Suominen, J., Pakarinen, M., Martelius, L., Heyman, S., Vervloessem, D., Steyaert, H., Sgrò, A., Gamba, P., Schurink, M., van der Heide, S., Roukema, J., Rikkers-Mutsaerts, N., Terheggen-Lagro, S., de Beer, S., Haarman, E., Till, H., Singer, G., Metzelder, M., Sezen, P, Desender, L., Schaballie, H., Cobanoglu, N., Gollu, G., Stanton, M., Bonnard, A., Sfeir, R., Muthialu, N., Mullassery, D., Wallis, C., Cox, D., Bagolan, P., Morini, F., Mesas Burgos, C., Conner, P., Caffrey Osvald, E., Bitkover, C., Decaluwé, H., Proesmans, M., Boon, M., Deprest, J., Gartner, S., Lain, A., Losty, P.D., Sinha, I., Yardley, I., Singh, M., Wessel, L., Zahn, K., Schaible, T., Qvist, N., Zampoli, M., Aksnes, G., van der Ent, C. K., Winter-de Groot, K.M., Peters, R., Hannon, E., Jöbsis, Q., Bannier, M.

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Lung disease in FLNA mutation: Confirmatory report von de Wit, M.C.Y, Tiddens, H.A.W.M, de Coo, I.F.M, Mancini, G.M.S

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Determining presence of lung disease in young children with cystic fibrosis: Lung clearance index, oxygen saturation and cough frequency von Bakker, E.M, van der Meijden, J.C, Nieuwhof, E.M, Hop, W.C.J, Tiddens, H.A.W.M

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Assessment of CF lung disease using motion corrected PROPELLER MRI: a comparison with CT von Ciet, Pierluigi, Serra, Goffredo, Bertolo, Silvia, Spronk, Sandra, Ros, Mirco, Fraioli, Francesco, Quattrucci, Serena, Assael, M. Baroukh, Catalano, Carlo, Pomerri, Fabio, Tiddens, Harm. A. W. M, Morana, Giovanni

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Novel strategies in newborn screening for cystic fibrosis: a prospective controlled study von Vernooij-van Langen, Annette M M, Loeber, J Gerard, Elvers, Bert, Triepels, Ralf H, Gille, Johan J P, Van der Ploeg, Catharina P B, Reijntjens, Sandra, Dompeling, Edward, Dankert-Roelse, Jeannette E

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Cost-effectiveness of newborn screening for cystic fibrosis determined with real-life data von van der Ploeg, C.P.B, van den Akker-van Marle, M.E, Vernooij-van Langen, A.M.M, Elvers, L.H, Gille, J.J.P, Verkerk, P.H, Dankert-Roelse, J.E

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Bronchodilation in infants with malacia or recurrent wheeze von Hofhuis, W, van der Wiel, E C, Tiddens, H A W M, Brinkhorst, G, Holland, W P J, de Jongste, J C, Merkus, P J F M

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