Communication in healthcare: a narrative review of the literature and practical recommendations von Vermeir, P., Vandijck, D., Degroote, S., Peleman, R., Verhaeghe, R., Mortier, E., Hallaert, G., Van Daele, S., Buylaert, W., Vogelaers, D.

Volltext

Long-term use of tube feeding in children with cystic fibrosis: results from two Belgian CF centers von Declercq, D., Huysentruyt, K., Hauser, B., De Wachter, E., Van daele, S., De Baets, F., Van Biervliet, S.

Volltext

Polymorphisms in the lectin pathway genes as a possible cause of early chronic Pseudomonas aeruginosa colonization in cystic fibrosis patients von Haerynck, F, Van Steen, K, Cattaert, T, Loeys, B, Van daele, S, Schelstraete, P, Claes, K, Van Thielen, M, De Canck, I, Mahachie John, J.M, De Baets, F

Volltext

Pseudomonas aeruginosa in the home environment of newly infected cystic fibrosis patients von Schelstraete, P, Van daele, S, De Boeck, K, Proesmans, M, Lebecque, P, Leclercq-Foucart, J, Malfroot, A, Vaneechoutte, M, De Baets, F

Volltext

Genetic variations in toll-like receptor pathway and lung function decline in Cystic Fibrosis patients von Haerynck, F, Mahachie John, J.M, Van Steen, K, Schelstraete, P, Van daele, S, Loeys, B, Van Thielen, M, De Canck, I, Nuytinck, L, De Baets, F

Volltext

Epidemiology of Pseudomonas aeruginosa in a cystic fibrosis rehabilitation centre von Van daele, S. G, Franckx, H, Verhelst, R, Schelstraete, P, Haerynck, F, Van Simaey, L, Claeys, G, Vaneechoutte, M, de Baets, F

Volltext

Survey of Pseudomonas aeruginosa genotypes in colonised cystic fibrosis patients von Van daele, S, Vaneechoutte, M, De Boeck, K, Knoop, C, Malfroot, A, Lebecque, P, Leclercq-Foucart, J, Van Schil, L, Desager, K, De Baets, F

Volltext

Role of nurses specializing in oncology to support the care journey for patients with penile cancer von De Keyser, C, Fele, I, Van Daele, S, Diamand, R, Peltier, A, Roumeguère, T

Volltext

Adding to the mix: a multilevel analysis of residential burglary von Peeters, M. P., Van Daele, S., Vander Beken, T.

Volltext

Malacia, inflammation and bronchoalveolar lavage culture in children with persistent respiratory symptoms von DE BAETS, F, DE SCHUTTER, L, AARTS, C, HAERYNCK, F, VAN DAELE, S, DE WACHTER, E, MALFROOT, A, SCHELSTRAETE, P

Volltext

286 Evaluation of HbA1c and OGTT-results after a first abnormal OGTT von Declercq, D, Van Daele, S, De Baets, F, Van Aken, S, Van Biervliet, S

Volltext

280 Single centre long-term experience with tube feeding in children with cystic fibrosis von Van Biervliet, S, Declercq, D, Van Daele, S, De Baets, F

Volltext

330 Characteristics at baseline of tube-fed cystic fibrosis (CF) patients with matched controls: a registry study von Libeert, D, Wanyama, S, Declercq, D, Thomas, M, Van Daele, S, De Baets, F, Van Biervliet, S

Volltext

WS05.7 Impact of tube feeding (TF) on pulmonary function in children and adults with cystic fibrosis von Libeert, D, Wanyama, S, Declercq, D, Thomas, M, Van Daele, S, De Baets, F, Van Biervliet, S

Volltext

WS05.6 The impact of tube feeding in children and adults with cystic fibrosis von Libeert, D, Wanyama, S, Declercq, D, Thomas, M, Van Daele, S, De Baets, F, Van Biervliet, S

Volltext

Achromobacter xylosoxidans induced bronchiolitis obliterans in cystic fibrosis von De Baets, F., Schelstraete, P., Haerynck, F., Van Biervliet, S., De Bruyne, R., Franckx, H., Van daele, S.

Volltext

81 Evaluation of the European Consensus Criteria for chronic colonization of CF patients with Pseudomonas aeruginosa by means of genotyping of consequent isolates von Jonckheere, L, Van Simaey, L, Van Braeckel, E, Schelstraete, P, Van Daele, S, De Baets, F, Vaneechoutte, M

Volltext

WS21.8 Validity of the Oxygen Uptake Efficiency Slope (OUES) as a parameter of maximal and submaximal exercise testing in children with mild CF von Cornette, J, Keyzer, M, Pyl, F, Coomans, I, Van Daele, S, Vandekerckhove, K

Volltext

192 ABPAs in Pseudomonas aeruginosa colonized CF patients von De Baets, F, De Keyzer, L, Schelstraete, P, Van Daele, S, Wanyama, S

Volltext

156 Exercise performance in children with mild cystic fibrosis (CF): Are there arguments to enhance physical activity? von Keyzer, M, Cornette, J, Pyl, F, Coomans, I, Van Daele, S, Vandekerckhove, K

Volltext