| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
Advancing the GI frontier for patients with CF
|
Freedman, Steven D.
|
|
2018
|
17 |
1 |
p. 1-2
|
artikel
|
| 2 |
Age-related levels of fecal M2-pyruvate kinase in children with cystic fibrosis and healthy children 0 to 10years old
|
Garg, Millie
|
|
2018
|
17 |
1 |
p. 109-113
|
artikel
|
| 3 |
Analytical and biological variation in repeated sweat chloride concentrations in clinical trials for CFTR modulator therapy
|
LeGrys, V.A.
|
|
2018
|
17 |
1 |
p. 43-49
|
artikel
|
| 4 |
Another step in the journey: From CFTR mutation to sweat chloride concentration to survival
|
VanDevanter, D.R.
|
|
2018
|
17 |
1 |
p. 3-4
|
artikel
|
| 5 |
Antibiotic exposure and interpersonal variance mask the effect of ivacaftor on respiratory microbiota composition
|
Peleg, Anton Y.
|
|
2018
|
17 |
1 |
p. 50-56
|
artikel
|
| 6 |
Caregiver burden of parents of young children with cystic fibrosis
|
Fitzgerald, C.
|
|
2018
|
17 |
1 |
p. 125-131
|
artikel
|
| 7 |
Combined lung-liver-pancreas transplantation in a recipient with cystic fibrosis
|
Barbas, A.S.
|
|
2018
|
17 |
1 |
p. e1-e4
|
artikel
|
| 8 |
Comparing the management of constipation and distal intestinal obstruction syndrome between paediatricians and adult physicians
|
Green, J.A.
|
|
2018
|
17 |
1 |
p. e6-e7
|
artikel
|
| 9 |
Complications of long and intermediate term venous catheters in cystic fibrosis patients: A multicenter study
|
May, Teresa L.
|
|
2018
|
17 |
1 |
p. 96-104
|
artikel
|
| 10 |
Detection of CFTR function and modulation in primary human nasal cell spheroids
|
Brewington, John J.
|
|
2018
|
17 |
1 |
p. 26-33
|
artikel
|
| 11 |
Drugs during pregnancy and breast feeding in women diagnosed with Cystic Fibrosis - An update
|
Kroon, M.A.G.M.
|
|
2018
|
17 |
1 |
p. 17-25
|
artikel
|
| 12 |
Editorial Board
|
|
|
2018
|
17 |
1 |
p. ii
|
artikel
|
| 13 |
Exercise and its varied impact on airway dynamics
|
Stevens, Daniel
|
|
2018
|
17 |
1 |
p. e5
|
artikel
|
| 14 |
Faecal calprotectin concentrations in young children with cystic fibrosis
|
Ellemunter, Helmut
|
|
2018
|
17 |
1 |
p. e8-e9
|
artikel
|
| 15 |
Fecal calprotectin concentrations in young children with cystic fibrosis: Authors response
|
Garg, Millie
|
|
2018
|
17 |
1 |
p. e10-e11
|
artikel
|
| 16 |
Gene editing & stem cells
|
Harrison, Patrick T.
|
|
2018
|
17 |
1 |
p. 10-16
|
artikel
|
| 17 |
Is there an association between back pain and stress incontinence in adults with cystic fibrosis? A retrospective cross-sectional study
|
Ashbrook, Jane E.
|
|
2018
|
17 |
1 |
p. 78-82
|
artikel
|
| 18 |
Let's talk about sex: Behaviors, experience and health care utilization in young women with CF
|
Heltshe, Sonya L.
|
|
2018
|
17 |
1 |
p. 5-6
|
artikel
|
| 19 |
Lower exhaled nitric oxide in infants with Cystic Fibrosis compared to healthy controls
|
Korten, Insa
|
|
2018
|
17 |
1 |
p. 105-108
|
artikel
|
| 20 |
Multiple prevalent fractures in relation to macroscopic bone architecture in patients with cystic fibrosis
|
Stahl, Mirjam
|
|
2018
|
17 |
1 |
p. 114-120
|
artikel
|
| 21 |
News
|
|
|
2018
|
17 |
1 |
p. 7-9
|
artikel
|
| 22 |
Recovery of lung function following a pulmonary exacerbation in patients with cystic fibrosis and the G551D-CFTR mutation treated with ivacaftor
|
Flume, Patrick A.
|
|
2018
|
17 |
1 |
p. 83-88
|
artikel
|
| 23 |
Retrospective observational study of French patients with cystic fibrosis and a Gly551Asp-CFTR mutation after 1 and 2years of treatment with ivacaftor in a real-world setting
|
Hubert, Dominique
|
|
2018
|
17 |
1 |
p. 89-95
|
artikel
|
| 24 |
Sexual and reproductive health behaviors and experiences reported by young women with cystic fibrosis
|
Kazmerski, Traci M.
|
|
2018
|
17 |
1 |
p. 57-63
|
artikel
|
| 25 |
Sexual and reproductive health care utilization and preferences reported by young women with cystic fibrosis
|
Kazmerski, Traci M.
|
|
2018
|
17 |
1 |
p. 64-70
|
artikel
|
| 26 |
The CF-CARES primary palliative care model: A CF-specific structured assessment of symptoms, distress, and coping
|
Friedman, Deborah
|
|
2018
|
17 |
1 |
p. 71-77
|
artikel
|
| 27 |
The relationship between sweat chloride levels and mortality in cystic fibrosis varies by individual genotype
|
Espel, Julia C.
|
|
2018
|
17 |
1 |
p. 34-42
|
artikel
|
| 28 |
The use of fructosamine in cystic fibrosis-related diabetes (CFRD) screening
|
Lam, Grace Y.
|
|
2018
|
17 |
1 |
p. 121-124
|
artikel
|
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