| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
Airway clearance therapy in the school environment: Retrospective analysis of a cohort of pediatric patients with cystic fibrosis
|
Byrwa, David J.
|
|
|
22 |
5 |
p. 811-815
|
artikel
|
| 2 |
Airway infections as a risk factor for Pseudomonas aeruginosa acquisition and chronic colonisation in children with cystic fibrosis
|
Mésinèle, Julie
|
|
|
22 |
5 |
p. 901-908
|
artikel
|
| 3 |
A multidisciplinary model for prenatal care for patients with cystic fibrosis in the era of highly effective modulator therapy
|
Li, Susan S
|
|
|
22 |
5 |
p. 806-810
|
artikel
|
| 4 |
A paradigm shift in cystic fibrosis nutritional care: Clinicians' views on the management of patients with overweight and obesity
|
Snowball, Joanna E
|
|
|
22 |
5 |
p. 836-842
|
artikel
|
| 5 |
Association between unplanned pregnancies and maternal exacerbations in cystic fibrosis
|
Peng, Giselle
|
|
|
22 |
5 |
p. 796-803
|
artikel
|
| 6 |
Association of Pseudomonas aeruginosa infection stage with lung function trajectory in children with cystic fibrosis
|
Rosenfeld, Margaret
|
|
|
22 |
5 |
p. 857-863
|
artikel
|
| 7 |
Automatic bronchus and artery analysis on chest computed tomography to evaluate the effect of inhaled hypertonic saline in children aged 3-6 years with cystic fibrosis in a randomized clinical trial
|
Chen, Yuxin
|
|
|
22 |
5 |
p. 916-925
|
artikel
|
| 8 |
Body composition and body mass index measures from 8 to 18 years old in children with cystic fibrosis
|
Tran, Jade K.
|
|
|
22 |
5 |
p. 851-856
|
artikel
|
| 9 |
Cervical mucus quality in females with and without cystic fibrosis
|
ROE, Andrea H.
|
|
|
22 |
5 |
p. 804-805
|
artikel
|
| 10 |
Cost-effectiveness analysis of genetic tools to predict treatment response in patients with cystic fibrosis
|
Sahakyan, Yeva
|
|
|
22 |
5 |
p. 933-940
|
artikel
|
| 11 |
Drug desensitization to lumacaftor/ivacaftor: A fast lane to drug tolerance
|
Westhoff, J.
|
|
|
22 |
5 |
p. 941-943
|
artikel
|
| 12 |
Editorial Board
|
|
|
|
22 |
5 |
p. ii
|
artikel
|
| 13 |
Effects of postage on recovery of pathogens from cystic fibrosis sputum samples
|
Hatfield, Lauren
|
|
|
22 |
5 |
p. 816-822
|
artikel
|
| 14 |
Ethnic differences in staphylococcus aureus acquisition in cystic fibrosis
|
McGarry, Meghan E.
|
|
|
22 |
5 |
p. 909-915
|
artikel
|
| 15 |
Exhaled breath profiles to detect lung infection with Staphylococcus aureus in children with cystic fibrosis
|
Licht, Johann-Christoph
|
|
|
22 |
5 |
p. 888-893
|
artikel
|
| 16 |
Exploration of the relationship between cumulative exposure to tobramycin and ototoxicity in patients with cystic fibrosis
|
Madaule, Justine
|
|
|
22 |
5 |
p. 944-948
|
artikel
|
| 17 |
Factors associated with lung function response with oral antibiotic treatment of pulmonary exacerbations in cystic fibrosis
|
Blanchard, Ana C.
|
|
|
22 |
5 |
p. 880-883
|
artikel
|
| 18 |
Food for thought: The revolution stirring within nutritional care priorities in cystic fibrosis
|
Sathe, Meghana N
|
|
|
22 |
5 |
p. 785-787
|
artikel
|
| 19 |
Impact of elexacaftor/tezacaftor/ivacaftor on fat-soluble vitamin levels in children with cystic fibrosis
|
Schembri, L
|
|
|
22 |
5 |
p. 843-846
|
artikel
|
| 20 |
Impact of lumacaftor/ivacaftor and tezacaftor/ivacaftor on treatment response in pulmonary exacerbations of F508del/F508del cystic fibrosis
|
McElvaney, Oliver J.
|
|
|
22 |
5 |
p. 875-879
|
artikel
|
| 21 |
Investigating Pseudomonas aeruginosa population structure and frequency of cross-infection in UK cystic fibrosis clinics - a reference laboratory perspective
|
Kenna, Dervla T.D.
|
|
|
22 |
5 |
p. 894-900
|
artikel
|
| 22 |
Managing women's health in CF: the birth of new challenges
|
Cohen, Raya
|
|
|
22 |
5 |
p. 783-784
|
artikel
|
| 23 |
Mobile health platform for self-management of pediatric cystic fibrosis: Impact on patient-centered care outcomes
|
Oates, Gabriela R.
|
|
|
22 |
5 |
p. 823-829
|
artikel
|
| 24 |
News article
|
Madge, Susan
|
|
|
22 |
5 |
p. 781-782
|
artikel
|
| 25 |
Nutritional considerations for a new era: A CF foundation position paper
|
Leonard, Amanda
|
|
|
22 |
5 |
p. 788-795
|
artikel
|
| 26 |
Partners in research: The success with therapies research consortium and the CF community unite to improve self-management
|
Sawicki, Gregory S.
|
|
|
22 |
5 |
p. 830-835
|
artikel
|
| 27 |
Prevalence, Risk Factors, and Sequelae of Asymptomatic Clostridioides difficile Colonization in Children with Cystic Fibrosis
|
Reasoner, Seth A.
|
|
|
22 |
5 |
p. 884-887
|
artikel
|
| 28 |
Re-examining baseline lung function recovery following IV-treated pulmonary exacerbations
|
Heltshe, Sonya L.
|
|
|
22 |
5 |
p. 864-867
|
artikel
|
| 29 |
Role of hyperglycemia in cystic fibrosis pulmonary exacerbations
|
Merjaneh, Lina
|
|
|
22 |
5 |
p. 868-874
|
artikel
|
| 30 |
Short-term structural and functional changes after airway clearance therapy in cystic fibrosis
|
West, Michael E.
|
|
|
22 |
5 |
p. 926-932
|
artikel
|
| 31 |
Traits, trends and hits of orphan drug designations in cystic fibrosis
|
Costa, Enrico
|
|
|
22 |
5 |
p. 949-957
|
artikel
|
| 32 |
Weight a minute: Exploring the effect on weight and body composition after the initiation of elexacaftor/tezacaftor/ivacaftor in adults with CF
|
Proud, David
|
|
|
22 |
5 |
p. 847-850
|
artikel
|
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