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                             27 gevonden resultaten
nr titel auteur tijdschrift jaar jaarg. afl. pagina('s) type
1 A novel guluronate oligomer improves intestinal transit and survival in cystic fibrosis mice Vitko, Megan
2016
15 6 p. 745-751
7 p.
artikel
2 A product of immunoreactive trypsinogen and pancreatitis-associated protein as second-tier strategy in cystic fibrosis newborn screening Weidler, Sophia
2016
15 6 p. 752-758
7 p.
artikel
3 Bioelectrical impedance in young patients with cystic fibrosis: Validation of a specific equation and clinical relevance Charatsi, A.M.
2016
15 6 p. 825-833
9 p.
artikel
4 Biomarkers for cystic fibrosis drug development Muhlebach, Marianne S.
2016
15 6 p. 714-723
10 p.
artikel
5 Bone demineralization is improved by ivacaftor in patients with cystic fibrosis carrying the p.Gly551Asp mutation Sermet-Gaudelus, Isabelle
2016
15 6 p. e67-e69
nvt p.
artikel
6 Continuous alternating inhaled antibiotics for chronic pseudomonal infection in cystic fibrosis Flume, Patrick A.
2016
15 6 p. 809-815
7 p.
artikel
7 Continuous alternating inhaled antibiotic therapy in CF: A single center retrospective analysis Van de Kerkhove, C.
2016
15 6 p. 802-808
7 p.
artikel
8 Coronary artery disease in cystic fibrosis: An emerging concern? Skolnik, Kate
2016
15 6 p. e70-e71
nvt p.
artikel
9 CT-abnormalities, bacteriology and symptoms of sinonasal disease in children with Cystic Fibrosis Berkhout, M.C.
2016
15 6 p. 816-824
9 p.
artikel
10 Cystic fibrosis biomarker — Commentary Durmowicz, Anthony G.
2016
15 6 p. 712-713
2 p.
artikel
11 Cystic fibrosis in Latin America—Improving the awareness Silva Filho, Luiz Vicente Ribeiro F.
2016
15 6 p. 791-793
3 p.
artikel
12 Early pulmonary disease manifestations in cystic fibrosis mice Darrah, Rebecca J.
2016
15 6 p. 736-744
9 p.
artikel
13 Editorial Board 2016
15 6 p. ii-
1 p.
artikel
14 Enteral tube feeding for individuals with cystic fibrosis: Cystic Fibrosis Foundation evidence-informed guidelines Schwarzenberg, Sarah Jane
2016
15 6 p. 724-735
12 p.
artikel
15 Equitable CF care as a basic human right De Boeck, Kris
2016
15 6 p. 703-704
2 p.
artikel
16 Eradication failure of newly acquired Pseudomonas aeruginosa isolates in cystic fibrosis Cohen-Cymberknoh, Malena
2016
15 6 p. 776-782
7 p.
artikel
17 Extensive cultivation of soil and water samples yields various pathogens in patients with cystic fibrosis but not Burkholderia multivorans Peeters, Charlotte
2016
15 6 p. 769-775
7 p.
artikel
18 IL-22 exacerbates weight loss in a murine model of chronic pulmonary Pseudomonas aeruginosa infection Bayes, Hannah K.
2016
15 6 p. 759-768
10 p.
artikel
19 Improving inhaled antibiotic treatment – Practice defeats the proof van der Ent, C Kors
2016
15 6 p. 705-707
3 p.
artikel
20 Long-term work participation among cystic fibrosis patients undergoing lung transplantation Krivchenia, Katelyn
2016
15 6 p. 846-849
4 p.
artikel
21 News 2016
15 6 p. 710-711
2 p.
artikel
22 Nutrition in CF — Two new important guidelines Wolfe, Susan P
2016
15 6 p. 708-709
2 p.
artikel
23 Probability of IV antibiotic retreatment within thirty days is associated with duration and location of IV antibiotic treatment for pulmonary exacerbation in cystic fibrosis VanDevanter, D.R.
2016
15 6 p. 783-790
8 p.
artikel
24 Respiratory pathogens mediate the association between lung function and temperature in cystic fibrosis Collaco, Joseph M.
2016
15 6 p. 794-801
8 p.
artikel
25 Sino nasal inhalation of isotonic versus hypertonic saline (6.0%) in CF patients with chronic rhinosinusitis — Results of a multicenter, prospective, randomized, double-blind, controlled trial Mainz, Jochen G.
2016
15 6 p. e57-e66
nvt p.
artikel
26 Ursodeoxycholic acid treatment is associated with improvement of liver stiffness in cystic fibrosis patients van der Feen, Cathelijne
2016
15 6 p. 834-838
5 p.
artikel
27 Variation of glucose tolerance in adult patients with cystic fibrosis: What is the potential contribution of insulin sensitivity? Boudreau, Valérie
2016
15 6 p. 839-845
7 p.
artikel
                             27 gevonden resultaten
 
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