| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
Acceptability and feasibility of a brief behavioral sleep intervention for youth with CF
|
Canter, Kimberly S.
|
|
|
22 |
1 |
p. 179-182
|
artikel
|
| 2 |
CFTR regulates brown adipocyte thermogenesis via the cAMP/PKA signaling pathway
|
Choi, Kyung-Mi
|
|
|
22 |
1 |
p. 132-139
|
artikel
|
| 3 |
Characterizing CFTR modulated sweat chloride response across the cf population: Initial results from the CHEC-SC study
|
Mayer-Hamblett, N
|
|
|
22 |
1 |
p. 79-88
|
artikel
|
| 4 |
Continuous glucose monitoring versus self-monitoring of blood glucose in the management of cystic fibrosis related diabetes: A systematic review and meta-analysis
|
Kumar, Shanal
|
|
|
22 |
1 |
p. 39-49
|
artikel
|
| 5 |
Cystic fibrosis related diabetes is not associated with maximal aerobic exercise capacity in cystic fibrosis: a cross-sectional analysis of an international multicenter trial
|
Radtke, Thomas
|
|
|
22 |
1 |
p. 31-38
|
artikel
|
| 6 |
Development and outcomes of a patient driven cystic fibrosis quality of care improvement project
|
Noordhoek, Jacquelien J.
|
|
|
22 |
1 |
p. 172-178
|
artikel
|
| 7 |
Different management approaches and outcome for infants with an inconclusive diagnosis following newborn screening for cystic fibrosis (CRMS/CFSPID) and Pseudomonas aeruginosa isolation
|
Dolce, Daniela
|
|
|
22 |
1 |
p. 73-78
|
artikel
|
| 8 |
Disparities in first evaluation of infants with cystic fibrosis since implementation of newborn screening
|
McColley, Susanna A.
|
|
|
22 |
1 |
p. 89-97
|
artikel
|
| 9 |
Early Glucose abnormalities in cystic fibrosis – how best to measure them, and what is to be done about them?
|
Hameed, Dr Shihab
|
|
|
22 |
1 |
p. 3-4
|
artikel
|
| 10 |
Editorial Board
|
|
|
|
22 |
1 |
p. ii
|
artikel
|
| 11 |
Evaluation of an association between RANKL and OPG with bone disease in people with cystic fibrosis
|
Abid, Shadaan
|
|
|
22 |
1 |
p. 140-145
|
artikel
|
| 12 |
Glycemic indices at night measured by CGM are predictive for a lower pulmonary function in adults but not in children with cystic fibrosis
|
Declercq, Dimitri
|
|
|
22 |
1 |
p. 59-65
|
artikel
|
| 13 |
Historical note: Horace Dobell's report of cystic fibrosis in 1872
|
Lubinsky, Mark
|
|
|
22 |
1 |
p. 183-184
|
artikel
|
| 14 |
Impact of antibiotic eradication therapy of Pseudomonas aeruginosa on long term lung function in cystic fibrosis
|
Casaredi, Isabel Gascon
|
|
|
22 |
1 |
p. 98-102
|
artikel
|
| 15 |
Insulinogenic index and early phase insulin secretion predict increased risk of worsening glucose tolerance and of cystic fibrosis-related diabetes
|
Potter, Kathryn J.
|
|
|
22 |
1 |
p. 50-58
|
artikel
|
| 16 |
In the Clear: Long-term pulmonary function benefits associated with Pseudomonas aeruginosa eradication
|
Dickinson, Kimberly M.
|
|
|
22 |
1 |
p. 7-8
|
artikel
|
| 17 |
Multi-omic comparisons between CFBE41o- cells stably expressing wild-type CFTR and F508del-mutant CFTR
|
Lu, Shiping
|
|
|
22 |
1 |
p. 146-155
|
artikel
|
| 18 |
Newborn screening for CF – The good, the bad and the ugly
|
Barben, Juerg
|
|
|
22 |
1 |
p. 5-6
|
artikel
|
| 19 |
News article
|
|
|
|
22 |
1 |
p. 1-2
|
artikel
|
| 20 |
Non-respiratory health-related quality of life in people with cystic fibrosis receiving elexacaftor/tezacaftor/ivacaftor
|
Fajac, Isabelle
|
|
|
22 |
1 |
p. 119-123
|
artikel
|
| 21 |
Prevalence, trends and outcomes of long-term inhaled antibiotic treatment in people with cystic fibrosis without chronic Pseudomonas aeruginosa infection – A European cystic fibrosis patient registry data analysis
|
Orenti, Annalisa
|
|
|
22 |
1 |
p. 103-111
|
artikel
|
| 22 |
Rapid chloride and bicarbonate determination by capillary electrophoresis for confirmatory testing of cystic fibrosis infants with volume-limited sweat specimens
|
Mathiaparanam, Stellena
|
|
|
22 |
1 |
p. 66-72
|
artikel
|
| 23 |
β-sitosterol ameliorates inflammation and Pseudomonas aeruginosa lung infection in a mouse model
|
Rossi, Alice
|
|
|
22 |
1 |
p. 156-160
|
artikel
|
| 24 |
Standards of care for CFTR variant-specific therapy (including modulators) for people with cystic fibrosis
|
Southern, Kevin W.
|
|
|
22 |
1 |
p. 17-30
|
artikel
|
| 25 |
Super resolution microscopy analysis reveals increased Orai1 activity in asthma and cystic fibrosis lungs
|
Goriounova, Alexandra S.
|
|
|
22 |
1 |
p. 161-171
|
artikel
|
| 26 |
Telehealth and CFTR modulators: Accelerating innovative models of cystic fibrosis care
|
Prickett, Michelle H.
|
|
|
22 |
1 |
p. 9-16
|
artikel
|
| 27 |
VOCAL: An observational study of ivacaftor for people with cystic fibrosis and selected non–G551D-CFTR gating mutations
|
Simmonds, Nicholas J.
|
|
|
22 |
1 |
p. 124-131
|
artikel
|
| 28 |
Ways of coping and survival in Cystic Fibrosis: a 20-year longitudinal study
|
Abbott, Janice
|
|
|
22 |
1 |
p. 112-118
|
artikel
|
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