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Journal of Pediatric Gastroenterology and Nutrition|July 20, 2010
Supplementation with fatty acids influences the airway nitric oxide and inflammatory markers in patients with cystic fibrosisChristina Keen, Anna-Carin Olin, Susanne Eriksson, et al.BMC Pulmonary Medicine|July 5, 2022
Persistent Aspergillus fumigatus infection in cystic fibrosis: impact on lung function and role of treatment of asymptomatic colonization-a registry-based case-control studyAxel Blomquist, Malin Inghammar, Mahasin Al Shakirchi, et al.The European Respiratory Journal|May 17, 2014
Paediatrics in BarcelonaFabio Midulla, Enrico Lombardi, Bart Rottier, et al.Pediatric Pulmonology|July 31, 2010
Gender differences in the Scandinavian cystic fibrosis populationHanne Vebert Olesen, Tacjana Pressler, Lena Hjelte, et al.Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|October 7, 2008
Diagnostic significance of measurements of specific IgG antibodies to Pseudomonas aeruginosa by three different serological methodsTacjana Pressler, Ferenc Karpati, Marta Granström, et al.Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|January 23, 2009
Differences in prevalence and treatment of Pseudomonas aeruginosa in cystic fibrosis centres in Denmark, Norway and SwedenPer Kristian Knudsen, Hanne V Olesen, Niels Høiby, et al.The European Respiratory Journal|February 25, 2012
Paediatrics in AmsterdamErnst Eber, Paul Aurora, Karin C Lødrup Carlsen, et al.Pediatric Pulmonology|January 14, 2022
Contemporary N2 and SF6 multiple breath washout in infants and toddlers with cystic fibrosisRikke M Sandvik, Per M Gustafsson, Anders Lindblad, et al.Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|April 5, 2021
Ursodeoxycholic acid and liver disease associated with cystic fibrosis: A multicenter cohort studyCarla Colombo, Gianfranco Alicandro, Mark Oliver, et al.Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|July 4, 2025
Pulmonary endpoints in clinical trials for children with cystic fibrosis under two years of ageTim Lee, Kate Hill, Daan Caudri, et al.Pageof 4