Journal of Cystic Fibrosis, 1569-1993

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  1. Clinical effects of the three CFTR potentiator treatments curcumin, genistein and ivacaftor in patients with the CFTR-S1251N gating mutation

    Berkers, G., van der Meer, R., van Mourik, P., Vonk, A. M., Kruisselbrink, E., Suen, S. W., Heijerman, H. G., Majoor, C. J., Koppelman, G. H., Roukema, J., Janssens, H. M., de Rijke, Y. B., Kemper, E. M., Beekman, J. M., van der Ent, C. K. & de Jonge, H. R., 1-Jun-2020, In : Journal of Cystic Fibrosis. 7 p.

    Research output: Contribution to journalArticleAcademicpeer-review

  2. Cirrhosis associated with decreased survival and a 10-year lower median age at death of cystic fibrosis patients in the Netherlands

    Pals, F. H., Verkade, H. J., Gulmans, V. A. M., De Koning, B. A. E., Koot, B. G. P., De Meij, T. G. J., Hendriks, D. M., Gierenz, N., Vreugdenhil, A. C. E., Houwen, R. H. J. & Bodewes, F. A. J. A., May-2019, In : Journal of Cystic Fibrosis. 18, 3, p. 385-389 5 p.

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  3. Ursodeoxycholate reduces cholate biosynthesis rate and pool

    Bodewes, F. A. J. A., Wouthuyzen-Bakker, M., Bijvelds, M., De Jonge, H. R. & Verkade, H. J., 1-Jun-2011, In : Journal of Cystic Fibrosis. 10, p. S69 1 p.

    Research output: Contribution to journalMeeting AbstractAcademic

  4. IVACAFTOR restores FGF19 regulated bile acid homeostasis in cystic fibrosis patients with an S1251N or a G551D gating mutation

    van de Peppel, I. P., Doktorova, M., Berkers, G., de Jonge, H. R., Houwen, R. H. J., Verkade, H. J., Jonker, J. W. & Bodewes, F. A. J. A., Mar-2019, In : Journal of Cystic Fibrosis. 18, 2, p. 286-293 8 p.

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  5. Bile acid homeostasis in gastrointestinal and metabolic complications of cystic fibrosis

    van de Peppel, I. P., Bodewes, F. A. J. A., Verkade, H. J. & Jonker, J. W., May-2019, In : Journal of Cystic Fibrosis. 18, 3, p. 313-320 8 p.

    Research output: Contribution to journalReview articleAcademicpeer-review

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