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The European Respiratory Journal|April 23, 2016
Optimal correction of distinct CFTR folding mutants in rectal cystic fibrosis organoidsJohanna F Dekkers, Ricardo A Gogorza Gondra, Evelien Kruisselbrink, et al.Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|February 17, 2020
R117H-CFTR function and response to VX-770 correlate with mRNA and protein expression in intestinal organoidsPeter Van Mourik, Paul van Haaren, Evelien Kruisselbrink, et al.International Journal of Neonatal Screening|December 22, 2023
Cystic Fibrosis Cases Missed by Newborn Bloodspot Screening-Towards a Consistent Definition and Data AcquisitionAnne Munck, Kevin W Southern, Jared Murphy, et al.Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|November 13, 2022
European survey of newborn bloodspot screening for CF: opportunity to address challenges and improve performanceAnne Munck, Daria O Berger, Kevin W Southern, et al.Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|May 11, 2016
Potentiator synergy in rectal organoids carrying S1251N, G551D, or F508del CFTR mutationsJohanna F Dekkers, Peter Van Mourik, Annelotte M Vonk, et al.Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|August 28, 2018
Newborn blood spot screening for cystic fibrosis with a four-step screening strategy in the NetherlandsJeannette E Dankert-Roelse, Marelle J Bouva, Bernadette S Jakobs, et al.Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|June 4, 2020
Development of the gut microbiota in early life: The impact of cystic fibrosis and antibiotic treatmentMaartje Kristensen, Sabine M P J Prevaes, Gino Kalkman, et al.Journal of Personalized Medicine|April 30, 2021
Individual and Group Response of Treatment with Ivacaftor on Airway and Gut Microbiota in People with CF and a S1251N MutationMaartje I Kristensen, Karin M de Winter-de Groot, Gitte Berkers, et al.Scientific Reports|October 31, 2023
Exploring intrinsic variability between cultured nasal and bronchial epithelia in cystic fibrosisLisa W Rodenburg, Mieke Metzemaekers, Isabelle S van der Windt, et al.Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|December 1, 2020
Updated guidance on the management of children with cystic fibrosis transmembrane conductance regulator-related metabolic syndrome/cystic fibrosis screen positive, inconclusive diagnosis (CRMS/CFSPID)Jürg Barben, Carlo Castellani, Anne Munck, et al.Pageof 4