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                             37 results found
no title author magazine year volume issue page(s) type
1 A phase I study assessing the safety and tolerability of allogeneic mesenchymal stem cell infusion in adults with cystic fibrosis Roesch, Erica A.

22 3 p. 407-413
article
2 Bariatric surgery in a patient with cystic fibrosis and diabetes: A case report Bruijn, N.R.A.

22 3 p. 577-579
article
3 Bone health outcomes in post-lung transplant patients with cystic fibrosis Tran, Triet Vincent M.

22 3 p. 381-387
article
4 Clinical outcomes of adults and children with cystic fibrosis during the COVID-19 pandemic Doumit, Michael

22 3 p. 581-586
article
5 Clinician perspectives on assessing for disordered eating and body image disturbance in adolescents and young adults with cystic fibrosis Kass, Alexandra P.

22 3 p. 431-435
article
6 Contemporary cystic fibrosis incidence rates in Canada and the United States Stephenson, Anne L.

22 3 p. 443-449
article
7 Cost burden among the CF population in the United States: A focus on debt, food insecurity, housing and health services Seyoum, Semret

22 3 p. 471-477
article
8 Cystic fibrosis in a transformative era: Adapting to changing mental health needs Landau, Eddie (Edwina) C.

22 3 p. 372-373
article
9 Cystic fibrosis prevalence in the United States and participation in the Cystic Fibrosis Foundation Patient Registry in 2020 Cromwell, Elizabeth A.

22 3 p. 436-442
article
10 Drug-drug interactions with CFTR modulator therapy in cystic fibrosis: Focus on Trikafta®/Kaftrio® Purkayastha, Debanjali

22 3 p. 478-483
article
11 Early life growth trajectories in cystic fibrosis are associated with lung function at age six Psoter, Kevin J.

22 3 p. 395-401
article
12 Editorial Board
22 3 p. ii
article
13 EFFECT OF ELEXACAFTOR/TEZACAFTOR/IVACAFTOR ON ANNUAL RATE OF LUNG FUNCTION DECLINE IN PEOPLE WITH CYSTIC FIBROSIS Lee, Tim

22 3 p. 402-406
article
14 European survey of newborn bloodspot screening for CF: opportunity to address challenges and improve performance Munck, Anne

22 3 p. 484-495
article
15 Factors associated with receiving CF care and use of telehealth in 2020 among persons with Cystic Fibrosis in the United States Collaco, JM

22 3 p. 456-463
article
16 FDA-approved drug screening in patient-derived organoids demonstrates potential of drug repurposing for rare cystic fibrosis genotypes de Poel, E.

22 3 p. 548-559
article
17 Growth trajectories in young children with cystic fibrosis: Where are we going? Sanders, Don B.

22 3 p. 370-371
article
18 High rates of anxiety detected in mothers of children with inconclusive cystic fibrosis screening results Ginsburg, Daniella K.

22 3 p. 420-426
article
19 Human papillomavirus prevalence, persistence and cervical dysplasia in females with cystic fibrosis Rousset-Jablonski, C.

22 3 p. 505-514
article
20 Lived experiences of people with cystic fibrosis that were not eligible for elexacaftor-tezacaftor-ivacaftor (ETI): A qualitative study Milo, Francesco

22 3 p. 414-419
article
21 Long-term tezacaftor/ivacaftor safety and efficacy in people with cystic fibrosis and an F508del-CFTR mutation: 96-week, open-label extension of the EXTEND trial Flume, Patrick A.

22 3 p. 464-470
article
22 News
22 3 p. 365-366
article
23 Position paper: Models of post-transplant care for individuals with cystic fibrosis McKone, Edward

22 3 p. 374-380
article
24 Regarding the article entitled “Effect of elexacaftor/tezacaftor/ivacaftor on annual rate of lung function decline in people with cystic fibrosis” Hoo, Zhe Hui

22 3 p. 587
article
25 Rescue by elexacaftor-tezacaftor-ivacaftor of the G1244E cystic fibrosis mutation's stability and gating defects are dependent on cell background Tomati, Valeria

22 3 p. 525-537
article
26 Steps Ahead: Optimising physical activity in adults with cystic fibrosis: A pilot randomised trial using wearable technology, goal setting and text message feedback Curran, Máire

22 3 p. 570-576
article
27 Suicide attempts in adolescents with cystic fibrosis on Elexacaftor/Tezacaftor/Ivacaftor therapy Arslan, Meliksah

22 3 p. 427-430
article
28 Targeted locus amplification reveals heterogeneity between and within CFTR genotypes and association with CFTR function in patient-derived intestinal organoids Lefferts, J.W.

22 3 p. 538-547
article
29 The influence of exocrine pancreatic function on the exposure and pharmacokinetics of ivacaftor in people with cystic fibrosis van der Meer, Renske

22 3 p. 564-569
article
30 The multi-faceted nature of 15 CFTR exonic variations: Impact on their functional classification and perspectives for therapy Bergougnoux, A.

22 3 p. 515-524
article
31 The risk of colorectal cancer in individuals with mutations of the cystic fibrosis transmembrane conductance regulator (CFTR) gene: An English population-based study Birch, Rebecca J.

22 3 p. 499-504
article
32 The use of dornase alfa in patients with COVID-19 Ramachandram, Dinesh Sangarran

22 3 p. 580
article
33 The U UGA C sequence provides a favorable context to ELX-02 induced CFTR readthrough Pranke, Iwona M.

22 3 p. 560-563
article
34 Trajectories of early growth and subsequent lung function in cystic fibrosis: An observational study using UK and Canadian registry data Macdougall, Amy

22 3 p. 388-394
article
35 Treatment effects of Elexacaftor/Tezacaftor/Ivacaftor in people with CF carrying non-F508del mutations Livnat, Galit

22 3 p. 450-455
article
36 Variability of the sweat test in children with Cystic Fibrosis previously CRMS/CFSPID: A retrospective monocenter experience Terlizzi, Vito

22 3 p. 496-498
article
37 When triple therapy is not working: A reverse iceberg perspective Castellani, Carlo

22 3 p. 367-369
article
                             37 results found
 
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