The effect of azithromycin on sputum inflammatory markers in bronchiectasis von Terpstra, L C, Altenburg, J, Doodeman, H J, Piñeros, Y S Sabogal, Lutter, R, Heijerman, H G M, Boersma, W G

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Forskolin induced swelling (FIS) assay in intestinal organoids to guide eligibility for compassionate use treatment in a CF patient with a rare genotype von Aalbers, B.L., Brunsveld, J.E., van der Ent, C.K., van den Eijnden, J.C., Beekman, J.M., Heijerman, H.G.M.

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Sinonasal manifestations of cystic fibrosis: A correlation between genotype and phenotype? von Berkhout, M.C, van Rooden, C.J, Rijntjes, E, Fokkens, W.J, el Bouazzaoui, L.H, Heijerman, H.G.M

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Effectiveness of pulmonary rehabilitation at high-altitude compared to sea-level in adults with severe refractory asthma von de Nijs, S.B., Krop, E.J.M., Portengen, L., Rijssenbeek-Nouwens, L.H., de Vries, D., Weersink, E.J.M., Heijerman, H.G.M., Heederik, D.J.J., Lammers, J.W.J.

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Dry powder inhalation of colistin sulphomethate in healthy volunteers: A pilot study von Westerman, E.M., de Boer, A.H., Le Brun, P.P.H., Touw, D.J., Frijlink, H.W., Heijerman, H.G.M.

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Clinical effect of lumacaftor/ivacaftor in F508del homozygous CF patients with FEV1 ≥ 90% predicted at baseline von Aalbers, B.L., de Winter-de Groot, K.M., Arets, H.G.M., Hofland, R.W., de Kiviet, A.C., van Oirschot-van de Ven, M.M.M., Kruijswijk, M.A., Schotman, S., Michel, S., van der Ent, C.K., Heijerman, H.G.M.

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Non-fasting bioelectrical impedance analysis in cystic fibrosis: Implications for clinical practice and research von Hollander-Kraaijeveld, F.M., Lindeman, Y., de Roos, N.M., Burghard, M., van de Graaf, E.A., Heijerman, H.G.M.

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Resting energy expenditure in cystic fibrosis patients decreases after lung transplantation, which improves applicability of prediction equations for energy requirement von Hollander-Kraaijeveld, F.M., van Lanen, A.S., de Roos, N.M., van de Graaf, E.A., Heijerman, H.G.M.

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Clinical impact of a highly prevalent Pseudomonas aeruginosa clone in Dutch cystic fibrosis patients von de Vrankrijker, A.M.M., Brimicombe, R.W., Wolfs, T.F.W., Heijerman, H.G.M., van Mansfeld, R., van Berkhout, F.T., Willems, R.J.L., Bonten, M.J.M., Ent, C. K. van der

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CT-abnormalities, bacteriology and symptoms of sinonasal disease in children with Cystic Fibrosis von Berkhout, M.C, Klerx-Melis, F, Fokkens, W.J, Nuijsink, M, van Aalderen, W.M.C, Heijerman, H.G.M

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Long-term effects of birth order and age at diagnosis in cystic fibrosis: A sibling cohort study von Slieker, M.G., van den Berg, J.M.W., Kouwenberg, J., van Berkhout, F. Teding, Heijerman, H.G.M., van der Ent, C.K.

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The BATTLE study: Effects of long-term tobramycin inhalation solution (TIS) once daily on exacerbation rate in patients with non-cystic fibrosis bronchiectasis. Study protocol of a... von Terpstra, L.C., Altenburg, J., Bronsveld, I., Doodeman, H.J., Rozemeijer, W., Heijerman, H.G.M., Boersma, W.G.

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Importance of bacteriology in upper airways of patients with Cystic Fibrosis von Berkhout, M.C, Rijntjes, E, el Bouazzaoui, L.H, Fokkens, W.J, Brimicombe, R.W, Heijerman, H.G.M

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Ivacaftor and sinonasal pathology in a cystic fibrosis patient with genotype deltaF508/S1215N von Vreede, C.L, Berkhout, M.C, Sprij, A.J, Fokkens, W.J, Heijerman, H.G.M

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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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Systemic absorption of nasally administered tobramycin and colistin in patients with cystic fibrosis von Berkhout, M C, van Velzen, A J, Touw, D J, de Kok, B M, Fokkens, W J, Heijerman, H G M

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Dry powder inhalation of colistin in cystic fibrosis patients: A single dose pilot study von Westerman, E.M, De Boer, A.H, Le Brun, P.P.H, Touw, D.J, Roldaan, A.C, Frijlink, H.W, Heijerman, H.G.M

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The influence of breathing mode on tobramycin serum levels using the I-neb AAD system in adults with cystic fibrosis von van Velzen, A.J, Uges, J.W.F, Le Brun, P.P.H, Shahbabai, P, Touw, D.J, Heijerman, H.G.M

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A productive cough von SCHILD, D, HEIJERMAN, H. G. M, SLEEBOOM, H. P

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Demographics of glucose metabolism in cystic fibrosis von van den Berg, J.M.W, Kouwenberg, J.M, Heijerman, H.G.M

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