nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
1 |
A comparison of clinic and home spirometry as longtudinal outcomes in cystic fibrosis
|
Paynter, Alex |
|
|
21 |
1 |
p. 78-83 |
artikel |
2 |
Acute ST-elevation myocardial infarction in two young women with cystic fibrosis and cystic fibrosis-related diabetes
|
Thambuluru, Sirisha Reddy |
|
|
21 |
1 |
p. e44-e47 |
artikel |
3 |
A Short extension to multiple breath washout provides additional signal of distal airway disease in people with CF: A pilot study
|
Short, Christopher |
|
|
21 |
1 |
p. 146-154 |
artikel |
4 |
Association between insurance variability and early lung function in children with cystic fibrosis
|
Dickinson, Kimberly M. |
|
|
21 |
1 |
p. 104-110 |
artikel |
5 |
Cardiovascular complications in cystic fibrosis: A review of the literature
|
Poore, T. Spencer |
|
|
21 |
1 |
p. 18-25 |
artikel |
6 |
Clinical characteristics of Pseudomonas and Aspergillus co-infected cystic fibrosis patients: A UK registry study
|
Hughes, Dominic A. |
|
|
21 |
1 |
p. 129-135 |
artikel |
7 |
Clinician variability in the diagnosis and treatment of aspergillus fumigatus-related conditions in cystic fibrosis: An international survey
|
Hong, Gina |
|
|
21 |
1 |
p. 136-142 |
artikel |
8 |
Comparing encounter-based and annualized chronic pseudomonas infection definitions in cystic fibrosis
|
Rosenfeld, Margaret |
|
|
21 |
1 |
p. 40-44 |
artikel |
9 |
Comparison of Cas9 and Cas12a CRISPR editing methods to correct the W1282X-CFTR mutation
|
Santos, Lúcia |
|
|
21 |
1 |
p. 181-187 |
artikel |
10 |
Comparison of microbial composition of cough swabs and sputum for pathogen detection in patients with cystic fibrosis
|
Fenn, Dominic |
|
|
21 |
1 |
p. 52-60 |
artikel |
11 |
Comparison of the readability of lay summaries and scientific abstracts published in CF Research News and the Journal of Cystic Fibrosis: Recommendations for writing lay summaries
|
Anderson, Hannah L. |
|
|
21 |
1 |
p. e11-e14 |
artikel |
12 |
Disease burden in people with cystic fibrosis heterozygous for F508del and a minimal function mutation
|
Sawicki, Gregory S. |
|
|
21 |
1 |
p. 96-103 |
artikel |
13 |
Editorial Board
|
|
|
|
21 |
1 |
p. ii |
artikel |
14 |
Effect of lumacaftor-ivacaftor on mucociliary clearance and clinical outcomes in cystic fibrosis: Results from the PROSPECT MCC sub-study
|
Donaldson, Scott H. |
|
|
21 |
1 |
p. 143-145 |
artikel |
15 |
Emergence and impact of oprD mutations in Pseudomonas aeruginosa strains in cystic fibrosis
|
Sherrard, Laura J. |
|
|
21 |
1 |
p. e35-e43 |
artikel |
16 |
Epigenome editing of the CFTR-locus for treatment of cystic fibrosis
|
Kabadi, Ami M. |
|
|
21 |
1 |
p. 164-171 |
artikel |
17 |
Health care costs related to home spirometry in the eICE randomized trial
|
Franz, Natalie |
|
|
21 |
1 |
p. 61-69 |
artikel |
18 |
HOMA indices as screening tests for cystic fibrosis-related diabetes
|
Toin, Tom |
|
|
21 |
1 |
p. 123-128 |
artikel |
19 |
Home monitoring for cystic fibrosis: The future is now
|
Moor, Catharina C. |
|
|
21 |
1 |
p. 15-17 |
artikel |
20 |
Impact of guideline-recommended dietitian assessments on weight gain in infants with cystic fibrosis
|
Ong, Thida |
|
|
21 |
1 |
p. 115-122 |
artikel |
21 |
Ivacaftor-elexacaftor-tezacaftor and tacrolimus combination in cystic fibrosis
|
Smith, Megan |
|
|
21 |
1 |
p. e8-e10 |
artikel |
22 |
Lack of CFTR alters the ferret pancreatic ductal epithelial secretome and cellular proteome: Implications for exocrine/endocrine signaling
|
Rotti, Pavana G. |
|
|
21 |
1 |
p. 172-180 |
artikel |
23 |
Longitudinal changes and regional variation of incident infection rates at cystic fibrosis centers, United States 2010-2016
|
Muhlebach, Marianne S. |
|
|
21 |
1 |
p. 34-39 |
artikel |
24 |
News article
|
|
|
|
21 |
1 |
p. 1-2 |
artikel |
25 |
No drug-drug interaction between tezacaftor-ivacaftor and clofazimine: A case report
|
Vonk, S.E.M. |
|
|
21 |
1 |
p. e5-e7 |
artikel |
26 |
Overweight and obesity in adults with cystic fibrosis: An Italian multicenter cohort study
|
Gramegna, Andrea |
|
|
21 |
1 |
p. 111-114 |
artikel |
27 |
Pathogen detection. The bread and butter
|
Forton, Julian T. |
|
|
21 |
1 |
p. 13-14 |
artikel |
28 |
Peripheral lung effect of elexacaftor/tezacaftor/ivacaftor in adult cystic fibrosis
|
Stylemans, Dimitri |
|
|
21 |
1 |
p. 160-163 |
artikel |
29 |
Preclinical atherosclerosis in cystic fibrosis: Two distinct presentations are related to pancreatic status
|
Nowak, Jan Krzysztof |
|
|
21 |
1 |
p. 26-33 |
artikel |
30 |
Quality of home spirometry performance amongst adults with cystic fibrosis
|
Bell, Jody M |
|
|
21 |
1 |
p. 84-87 |
artikel |
31 |
Real-world assessment of LCI following lumacaftor-ivacaftor initiation in adolescents and adults with cystic fibrosis
|
Reix, Philippe |
|
|
21 |
1 |
p. 155-159 |
artikel |
32 |
Retracing changes in cystic fibrosis understanding and management over the past twenty years
|
Ratjen, Felix |
|
|
21 |
1 |
p. 3-9 |
artikel |
33 |
Risk factors for Pseudomonas aeruginosa airway infection and lung function decline in children with cystic fibrosis
|
Mésinèle, Julie |
|
|
21 |
1 |
p. 45-51 |
artikel |
34 |
Satisfaction and effectiveness of opioid pain management among adults with cystic fibrosis: A mixed methods study
|
Allgood, Sarah |
|
|
21 |
1 |
p. e15-e22 |
artikel |
35 |
Targeted exhaled breath analysis for detection of Pseudomonas aeruginosa in cystic fibrosis patients
|
Kos, Renate |
|
|
21 |
1 |
p. e28-e34 |
artikel |
36 |
Temporal trends in healthcare resource use and associated costs of patients with cystic fibrosis
|
Durieu, Isabelle |
|
|
21 |
1 |
p. 88-95 |
artikel |
37 |
The feasibility of home monitoring of young people with cystic fibrosis: Results from CLIMB-CF
|
Edmondson, C. |
|
|
21 |
1 |
p. 70-77 |
artikel |
38 |
The journal of cystic fibrosis’ 20th anniversary
|
De Boeck, Kris |
|
|
21 |
1 |
p. 10-12 |
artikel |
39 |
Urinary tract infections in cystic fibrosis patients
|
Reasoner, Seth A. |
|
|
21 |
1 |
p. e1-e4 |
artikel |
40 |
When CFSPID becomes CF
|
Ginsburg, Daniella |
|
|
21 |
1 |
p. e23-e27 |
artikel |