A case report of an unusual non-mucinous papillary variant of CPAM type 1 with KRAS mutations by Timco Koopman, Bart L. Rottier, Arja ter Elst, Wim Timens

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Prerequisites for a dry powder inhaler for children with cystic fibrosis. by Anne J Lexmond, Paul Hagedoorn, Henderik W Frijlink, Bart L Rottier, Anne H de Boer

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Monitoring asthma in childhood: management-related issues by Bart L. Rottier, Ernst Eber, Gunilla Hedlin, Steve Turner, Edwina Wooler, Eva Mantzourani, Neeta Kulkarni

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Effect of inhaler design variables on paediatric use of dry powder inhalers. by Anne J Lexmond, Tonnis J Kruizinga, Paul Hagedoorn, Bart L Rottier, Henderik W Frijlink, Anne H de Boer

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Remote monitoring and teleconsultations can reduce greenhouse gas emissions while maintaining quality of care in cystic fibrosis by Martinus C. Oppelaar, Michiel A. G. E. Bannier, Monique H. E. Reijers, Hester van der Vaart, Renske van der Meer, Josje Altenburg, Lennart Conemans, Lennart Conemans, Bart L. Rottier, Bart L. Rottier, Marianne Nuijsink, Lara S. van den Wijngaart, Peter J. F. M. Merkus, Jolt Roukema

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Key paediatric messages from the 2016 European Respiratory Society International Congress by Jonathan Grigg, Ian M. Balfour-Lynn, Mark Everard, Graham Hall, Bülent Karadag, Kostas Priftis, Charles Christoph Roehr, Bart L. Rottier, Fabio Midulla

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Eradication of Burkholderia cepacia complex in cystic fibrosis patients with inhalation of amiloride and tobramycin combined with oral cotrimoxazole by Anne M. Akkerman-Nijland, Bart L. Rottier, Joanne Holstein, Rik L.J. Winter, Daniel J. Touw, Onno W. Akkerman, Gerard H. Koppelman

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Correction: Tolerance of Organ Transplant Recipients to Physical Activity during a High-Altitude Expedition: Climbing Mount Kilimanjaro. by Edwin J van Adrichem, Marion J Siebelink, Bart L Rottier, Janneke M Dilling, Greetje Kuiken, Cees P van der Schans, Erik A M Verschuuren

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Tolerance of Organ Transplant Recipients to Physical Activity during a High-Altitude Expedition: Climbing Mount Kilimanjaro. by Edwin J van Adrichem, Marion J Siebelink, Bart L Rottier, Janneke M Dilling, Greetje Kuiken, Cees P van der Schans, Erik A M Verschuuren

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Eradication of in cystic fibrosis patients with inhalation of dry powder tobramycin by Anne M. Akkerman-Nijland, Mina Yousofi, Bart L. Rottier, Hester Van der Vaart, Johannes G. M. Burgerhof, Henderik W. Frijlink, Daan J. Touw, Gerard H. Koppelman, Onno W. Akkerman

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The Long-Term Uptake of Home Spirometry in Regular Cystic Fibrosis Care: Retrospective Multicenter Observational Study by Pia Bertram, Martinus C Oppelaar, Michiel AGE Bannier, Monique HE Reijers, Hester van der Vaart, Renske van der Meer, Josje Altenburg, Lennart Conemans, Bart L Rottier, Marianne Nuijsink, Lara S van den Wijngaart, Peter JFM Merkus, Jolt Roukema

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Accuracy, Reproducibility, and Responsiveness to Treatment of Home Spirometry in Cystic Fibrosis: Multicenter, Retrospective, Observational Study by Martinus C Oppelaar, Hanneke AC van Helvoort, Michiel AGE Bannier, Monique HE Reijers, Hester van der Vaart, Renske van der Meer, Josje Altenburg, Lennart Conemans, Bart L Rottier, Marianne Nuijsink, Lara S van den Wijngaart, Peter JFM Merkus, Jolt Roukema

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Potential, Pitfalls, and Future Directions for Remote Monitoring of Chronic Respiratory Diseases: Multicenter Mixed Methods Study in Routine Cystic Fibrosis Care by Martinus C Oppelaar, Yvette Emond, Michiel A G E Bannier, Monique H E Reijers, Hester van der Vaart, Renske van der Meer, Josje Altenburg, Lennart Conemans, Bart L Rottier, Marianne Nuijsink, Lara S van den Wijngaart, Peter J F M Merkus, Maud Heinen, Jolt Roukema

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