| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
Abnormal glucose tolerance and the 50-gram glucose challenge test in Cystic fibrosis
|
Sheikh, Saba
|
|
|
19 |
5 |
p. 696-699
|
artikel
|
| 2 |
Accumulation and persistence of ivacaftor in airway epithelia with prolonged treatment
|
Guhr Lee, Tara N.
|
|
|
19 |
5 |
p. 746-751
|
artikel
|
| 3 |
Amplifiers co-translationally enhance CFTR biosynthesis via PCBP1-mediated regulation of CFTR mRNA
|
Dukovski, Danijela
|
|
|
19 |
5 |
p. 733-741
|
artikel
|
| 4 |
Answering the call to address cystic fibrosis treatment burden in the era of highly effective CFTR modulator therapy
|
Gifford, Alex H.
|
|
|
19 |
5 |
p. 762-767
|
artikel
|
| 5 |
Anti-inflammatory effects of lenabasum, a cannabinoid receptor type 2 agonist, on macrophages from cystic fibrosis
|
Tarique, Abdullah A.
|
|
|
19 |
5 |
p. 823-829
|
artikel
|
| 6 |
Building global development strategies for cf therapeutics during a transitional cftr modulator era
|
Mayer-Hamblett, N.
|
|
|
19 |
5 |
p. 677-687
|
artikel
|
| 7 |
Comment on "Effect of one-year lumacaftor-ivacaftor treatment on glucose tolerance abnormalities in cystic fibrosis patients"
|
Ballmann, Manfred
|
|
|
19 |
5 |
p. 839
|
artikel
|
| 8 |
Cystic fibrosis drug trial design in the era of CFTR modulators associated with substantial clinical benefit: stakeholders’ consensus view
|
De Boeck, K.
|
|
|
19 |
5 |
p. 688-695
|
artikel
|
| 9 |
Cystic fibrosis related diabetes: Revisiting the OGTT and alternate screening tests
|
Chan, Christine L.
|
|
|
19 |
5 |
p. 671-672
|
artikel
|
| 10 |
Dyslipidemia is not associated with the development of glucose intolerance or diabetes in cystic fibrosis
|
Colomba, Johann
|
|
|
19 |
5 |
p. 704-711
|
artikel
|
| 11 |
Editorial Board
|
|
|
|
19 |
5 |
p. ii
|
artikel
|
| 12 |
Effect of one-year lumacaftor–ivacaftor treatment on glucose tolerance abnormalities in cystic fibrosis patients
|
Misgault, Bastien
|
|
|
19 |
5 |
p. 712-716
|
artikel
|
| 13 |
Eligibility of CFTR modulators for the adult-diagnosed cystic fibrosis population
|
Desai, Sameer
|
|
|
19 |
5 |
p. 840-841
|
artikel
|
| 14 |
Endobronchial valve treatment of persistent alveolopleural fistulae in a patient with cystic fibrosis and empyema
|
Bongers, Kale S.
|
|
|
19 |
5 |
p. e36-e38
|
artikel
|
| 15 |
Fibrocyte accumulation in the lungs of cystic fibrosis patients
|
Kasam, Rajesh K.
|
|
|
19 |
5 |
p. 815-822
|
artikel
|
| 16 |
Formative evaluation of a dashboard to support coproduction of healthcare services in cystic fibrosis
|
Van Citters, Aricca D.
|
|
|
19 |
5 |
p. 768-776
|
artikel
|
| 17 |
From disease mechanisms to novel therapies and back
|
Farinha, Carlos M.
|
|
|
19 |
5 |
p. 673-674
|
artikel
|
| 18 |
Functional rescue of c.3846G>A (W1282X) in patient-derived nasal cultures achieved by inhibition of nonsense mediated decay and protein modulators with complementary mechanisms of action
|
Laselva, Onofrio
|
|
|
19 |
5 |
p. 717-727
|
artikel
|
| 19 |
Glucose abnormalities detected by continuous glucose monitoring are common in young children with Cystic Fibrosis
|
Prentice, Bernadette J.
|
|
|
19 |
5 |
p. 700-703
|
artikel
|
| 20 |
Influenza B outbreak at an adult cystic fibrosis centre - Clinical impact and factors influencing spread
|
Dennis, Jordan B
|
|
|
19 |
5 |
p. 808-814
|
artikel
|
| 21 |
In the south, if you give us lemons, we will make you lemonade
|
Garcia, Bryan
|
|
|
19 |
5 |
p. 842-843
|
artikel
|
| 22 |
Intrinsic alterations in peripheral neutrophils from cystic fibrosis newborn piglets
|
Bréa, Déborah
|
|
|
19 |
5 |
p. 830-836
|
artikel
|
| 23 |
In vitro 3D culture lung model from expanded primary cystic fibrosis human airway cells
|
Rayner, Rachael E.
|
|
|
19 |
5 |
p. 752-761
|
artikel
|
| 24 |
Metabolomics profiling of tobacco exposure in children with cystic fibrosis
|
Wisniewski, Benjamin L.
|
|
|
19 |
5 |
p. 791-800
|
artikel
|
| 25 |
News Article
|
|
|
|
19 |
5 |
p. 675-676
|
artikel
|
| 26 |
New therapies for people with CF in the CFTR modulator world
|
Wainwright, Claire E
|
|
|
19 |
5 |
p. 669-670
|
artikel
|
| 27 |
No detection of SARS-CoV-2 in cystic fibrosis patients at the Regional (Lazio) Reference Center for CF in Italy
|
Scagnolari, Carolina
|
|
|
19 |
5 |
p. 837-838
|
artikel
|
| 28 |
Organizing pneumonia secondary to Exophiala dermatitidis in cystic fibrosis: A case report
|
Radonjic, Aleksandar
|
|
|
19 |
5 |
p. e33-e35
|
artikel
|
| 29 |
R117H-CFTR function and response to VX-770 correlate with mRNA and protein expression in intestinal organoids
|
Van Mourik, Peter
|
|
|
19 |
5 |
p. 728-732
|
artikel
|
| 30 |
Sleep disturbance and sleep insufficiency in primary caregivers and their children with cystic fibrosis
|
Byars, Kelly C.
|
|
|
19 |
5 |
p. 777-782
|
artikel
|
| 31 |
Testicular pain following initiation of elexacaftor/tezacaftor/ivacaftor in males with cystic fibrosis
|
Rotolo, Shannon M.
|
|
|
19 |
5 |
p. e39-e41
|
artikel
|
| 32 |
The specialist as primary care provider in CF
|
Haywood, Kelsey B.
|
|
|
19 |
5 |
p. 844-845
|
artikel
|
| 33 |
Tobacco smoke exposure and socioeconomic factors are independent predictors of pulmonary decline in pediatric cystic fibrosis
|
Oates, Gabriela R.
|
|
|
19 |
5 |
p. 783-790
|
artikel
|
| 34 |
Urine lipoarabinomannan as a marker for low-risk of NTM infection in the CF airway
|
De, Prithwiraj
|
|
|
19 |
5 |
p. 801-807
|
artikel
|
| 35 |
Variable cellular ivacaftor concentrations in people with cystic fibrosis on modulator therapy
|
Guimbellot, Jennifer S.
|
|
|
19 |
5 |
p. 742-745
|
artikel
|
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