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F De Baets

Showing results (21-30 of 35) with videos related to

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American Journal of Respiratory and Critical Care Medicine|November 9, 2000
Cystic fibrosis sputum: a barrier to the transport of nanospheresN N Sanders, S C De Smedt, E Van Rompaey, et al.
European Journal of Clinical Nutrition|October 20, 2020
Long-term use of tube feeding in children with cystic fibrosis: results from two Belgian CF centersD Declercq, K Huysentruyt, B Hauser, et al.
Human Mutation|January 1, 1997
Analysis of 22 cystic fibrosis mutations in 62 patients from the Flanders, Belgium, reveals a high prevalence of Nordic mutation 394delTTL Messiaen, C Van Loon, R Rossau, et al.
Journal of Public Health (Oxford, England)|August 7, 2007
Smoking in young people with asthmaA Hublet, D De Bacquer, W Boyce, et al.
Pediatric Pulmonology|September 17, 2013
Achromobacter xylosoxidans induced bronchiolitis obliterans in cystic fibrosisF De Baets, P Schelstraete, F Haerynck, et al.
Journal of Medical Genetics|November 1, 1990
A child, homozygous for a stop codon in exon 11, shows milder cystic fibrosis symptoms than her heterozygous nephewH Cuppens, P Marynen, C De Boeck, et al.
The European Respiratory Journal|July 23, 2011
Malacia, inflammation and bronchoalveolar lavage culture in children with persistent respiratory symptomsF De Baets, I De Schutter, C Aarts, et al.
Acta Gastro-Enterologica Belgica|February 18, 2017
Gastro-intestinal manifestations in cystic fibrosis patientsS Van Biervliet, C de Clercq, D Declercq, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|October 8, 2008
Early referral to cystic fibrosis specialist centre impacts on respiratory outcomeP Lebecque, A Leonard, K De Boeck, et al.
The European Respiratory Journal|March 2, 2005
Epidemiology of Pseudomonas aeruginosa in a cystic fibrosis rehabilitation centreS G Van Daele, H Franckx, R Verhelst, et al.
Pageof 4

Showing results (21-30 of 35) with videos related to

Sort By:
Pageof 4
American Journal of Respiratory and Critical Care Medicine|November 9, 2000
Cystic fibrosis sputum: a barrier to the transport of nanospheresN N Sanders, S C De Smedt, E Van Rompaey, et al.
European Journal of Clinical Nutrition|October 20, 2020
Long-term use of tube feeding in children with cystic fibrosis: results from two Belgian CF centersD Declercq, K Huysentruyt, B Hauser, et al.
Human Mutation|January 1, 1997
Analysis of 22 cystic fibrosis mutations in 62 patients from the Flanders, Belgium, reveals a high prevalence of Nordic mutation 394delTTL Messiaen, C Van Loon, R Rossau, et al.
Journal of Public Health (Oxford, England)|August 7, 2007
Smoking in young people with asthmaA Hublet, D De Bacquer, W Boyce, et al.
Pediatric Pulmonology|September 17, 2013
Achromobacter xylosoxidans induced bronchiolitis obliterans in cystic fibrosisF De Baets, P Schelstraete, F Haerynck, et al.
Journal of Medical Genetics|November 1, 1990
A child, homozygous for a stop codon in exon 11, shows milder cystic fibrosis symptoms than her heterozygous nephewH Cuppens, P Marynen, C De Boeck, et al.
The European Respiratory Journal|July 23, 2011
Malacia, inflammation and bronchoalveolar lavage culture in children with persistent respiratory symptomsF De Baets, I De Schutter, C Aarts, et al.
Acta Gastro-Enterologica Belgica|February 18, 2017
Gastro-intestinal manifestations in cystic fibrosis patientsS Van Biervliet, C de Clercq, D Declercq, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|October 8, 2008
Early referral to cystic fibrosis specialist centre impacts on respiratory outcomeP Lebecque, A Leonard, K De Boeck, et al.
The European Respiratory Journal|March 2, 2005
Epidemiology of Pseudomonas aeruginosa in a cystic fibrosis rehabilitation centreS G Van Daele, H Franckx, R Verhelst, et al.
Pageof 4