ePS04.3 CF patients' pain experience with different sampling methods for bacterial culture
Eyns, H, Galasso, N, De Wachter, E, Malfroot, A
Published in Journal of cystic fibrosis (01.06.2016)
Published in Journal of cystic fibrosis (01.06.2016)
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Journal Article
WS08.2/2 Use of the AKITA JET for inhalation treatment in cystic fibrosis – Part II: Patients’ satisfaction
Eyns, H, Willekens, J, Opdekamp, C, Van Hove, O, Gaspar, V, Galasso, C, Vanderhelst, E, Hanssens, L, Knoop, C, Malfroot, A
Published in Journal of cystic fibrosis (01.06.2015)
Published in Journal of cystic fibrosis (01.06.2015)
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Journal Article
WS08.2/1 Use of the AKITA JET for inhalation treatment in cystic fibrosis – Part I: Clinical outcomes
Eyns, H, Willekens, J, Gaspar, V, Opdekamp, C, Van Hove, O, Galasso, C, Vanderhelst, E, Hanssens, L, Knoop, C, Malfroot, A
Published in Journal of cystic fibrosis (01.06.2015)
Published in Journal of cystic fibrosis (01.06.2015)
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Journal Article
105 Adaptation of Pseudomonas aeruginosa in the CF host: Link between laboratory findings and the clinic?
Willekens, J, Dingemans, J, Eyns, H, Crabbé, A, Cornelis, P, Malfroot, A
Published in Journal of cystic fibrosis (01.06.2013)
Published in Journal of cystic fibrosis (01.06.2013)
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Journal Article
149 Epidemiology and clinical impact of Burkholderia cepacia complex: A single-centre analysis
Willekens, J, Eyns, H, De Wachter, E, De Schutter, I, De Bel, A, Echahidi, F, Malfroot, A
Published in Journal of cystic fibrosis (01.06.2013)
Published in Journal of cystic fibrosis (01.06.2013)
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135 The use of rep-PCR (Diversilab, bioMerieux) in combination with multiplex PCR (targeting virulence genes) reveals the transmission of Pseudomonas aeruginosa isolates among cystic fibrosis patients in a hospital background
Dingemans, J, Craggs, M, Bilocq, F, Willekens, J, Eyns, H, Crabbé, A, De Vos, D, Pirnay, J.-P, Malfroot, A, Cornelis, P
Published in Journal of cystic fibrosis (01.06.2013)
Published in Journal of cystic fibrosis (01.06.2013)
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244 Influence of inhaled hypertonic saline (NaCI 6%) before or during autogenic drainage on sputum weight, oxygen saturation, heart frequency and dyspnoea in cystic fibrosis patients
Van Ginderdeuren, F, Vanlaethem, S, Eyns, H, De Schutter, I, Dewachter, E, Malfroot, A
Published in Journal of cystic fibrosis (2011)
Published in Journal of cystic fibrosis (2011)
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Journal Article
P390 Ageing with cystic fibrosis: challenges for patients and team members
Braun, S., Eyns, H., Vincken, S., De Wachter, E., Vanderhelst, E.
Published in Journal of cystic fibrosis (01.06.2023)
Published in Journal of cystic fibrosis (01.06.2023)
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Journal Article
P243 Psychosocial impact of 6 months of treatment with Symkevi® among adult cystic fibrosis patients
Braun, S., Eyns, H., Verbanck, S., Vanderhelst, E., Knoop, C., De Wachter, E., Vincken, S.
Published in Journal of cystic fibrosis (01.06.2022)
Published in Journal of cystic fibrosis (01.06.2022)
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Journal Article
P362 A Belgian survey comparing the knowledge of cystic fibrosis in 2 different groups of teenagers
Braun, S., Eyns, H., Daelemans, S., Peeters, L., De Wachter, E.
Published in Journal of cystic fibrosis (01.06.2020)
Published in Journal of cystic fibrosis (01.06.2020)
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