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American Journal of Respiratory and Critical Care Medicine
|
November 9, 2000
Cystic fibrosis sputum: a barrier to the transport of nanospheres
N 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 centers
D 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 394delTT
L Messiaen, C Van Loon, R Rossau, et al.
Journal of Public Health (Oxford, England)
|
August 7, 2007
Smoking in young people with asthma
A Hublet, D De Bacquer, W Boyce, et al.
Pediatric Pulmonology
|
September 17, 2013
Achromobacter xylosoxidans induced bronchiolitis obliterans in cystic fibrosis
F 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 nephew
H 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 symptoms
F De Baets, I De Schutter, C Aarts, et al.
Acta Gastro-Enterologica Belgica
|
February 18, 2017
Gastro-intestinal manifestations in cystic fibrosis patients
S 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 outcome
P Lebecque, A Leonard, K De Boeck, et al.
The European Respiratory Journal
|
March 2, 2005
Epidemiology of Pseudomonas aeruginosa in a cystic fibrosis rehabilitation centre
S G Van Daele, H Franckx, R Verhelst, et al.
Page
of 4
Search research articles
Search
Showing results (21-30 of 35) with videos related to
Sort By:
Page
of 4
American Journal of Respiratory and Critical Care Medicine
|
November 9, 2000
Cystic fibrosis sputum: a barrier to the transport of nanospheres
N 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 centers
D 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 394delTT
L Messiaen, C Van Loon, R Rossau, et al.
Journal of Public Health (Oxford, England)
|
August 7, 2007
Smoking in young people with asthma
A Hublet, D De Bacquer, W Boyce, et al.
Pediatric Pulmonology
|
September 17, 2013
Achromobacter xylosoxidans induced bronchiolitis obliterans in cystic fibrosis
F 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 nephew
H 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 symptoms
F De Baets, I De Schutter, C Aarts, et al.
Acta Gastro-Enterologica Belgica
|
February 18, 2017
Gastro-intestinal manifestations in cystic fibrosis patients
S 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 outcome
P Lebecque, A Leonard, K De Boeck, et al.
The European Respiratory Journal
|
March 2, 2005
Epidemiology of Pseudomonas aeruginosa in a cystic fibrosis rehabilitation centre
S G Van Daele, H Franckx, R Verhelst, et al.
Page
of 4