Tang C, Zhou J, Song Y, Liu S
Gastroenterol Rep (Oxf). 2025; 13:goaf019.
PMID: 40066317
PMC: 11893156.
DOI: 10.1093/gastro/goaf019.
Davis J, Perkins R, Bailey J, Chaudary N, Garcia B, Froh D
Pediatr Pulmonol. 2025; 60(2):e70000.
PMID: 39960328
PMC: 11890385.
DOI: 10.1002/ppul.70000.
Poamaneagra S, Plesca D, Tataranu E, Marginean O, Nemtoi A, Mihai C
J Clin Med. 2024; 13(23).
PMID: 39685886
PMC: 11642410.
DOI: 10.3390/jcm13237428.
Hinton A, Sears E, Zuckerman J, Lopez-Pintado S
PLoS One. 2024; 19(12):e0313510.
PMID: 39625878
PMC: 11614261.
DOI: 10.1371/journal.pone.0313510.
Enochs C, Filbrun A, Hjelm M, Lehrmann J, Mullen L, Packard R
Pediatr Pulmonol. 2024; 60(1):e27326.
PMID: 39441068
PMC: 11733705.
DOI: 10.1002/ppul.27326.
IL1B gene variants, but not TNF, CXCL8, IL6 and IL10, modify the course of cystic fibrosis in Polish patients.
Zakerska-Banaszak O, Gozdzik-Spychalska J, Gabryel M, Zuraszek J, Skrzypczak-Zielinska M, Slomski R
F1000Res. 2024; 11:379.
PMID: 39185143
PMC: 11344199.
DOI: 10.12688/f1000research.110472.3.
Cystic Fibrosis in Adults: A Paradigm of Frailty Syndrome? An Observational Study.
Iacotucci P, Carnovale V, Ferrillo L, Somma J, Bocchino M, DIppolito M
J Clin Med. 2024; 13(2).
PMID: 38276090
PMC: 10816671.
DOI: 10.3390/jcm13020585.
Screening for Cystic Fibrosis Related Complications in the Context of a Pandemic and Altered Models of Care.
Doumit M, Strachan R, Lazarus R, Middleton P, Dentice R, Marouvo J
Health Serv Insights. 2023; 16:11786329231205145.
PMID: 37854074
PMC: 10580724.
DOI: 10.1177/11786329231205145.
Modified forced expiration technique using expiratory resistance in adults with cystic fibrosis.
Watson K, Koenig E, Bannister A, Mayne V, Jacques A, Sawyer A
Clin Respir J. 2023; 17(11):1196-1199.
PMID: 37793978
PMC: 10632078.
DOI: 10.1111/crj.13708.
Falling through the Cracks-The Impact of Care Gaps on Lung Function Loss in Cystic Fibrosis.
Love A, Quon B
Ann Am Thorac Soc. 2023; 20(9):1235-1236.
PMID: 37655958
PMC: 10502880.
DOI: 10.1513/AnnalsATS.202305-459ED.
Reproductive Counseling and Care in Cystic Fibrosis: A Multidisciplinary Approach for a New Therapeutic Era.
McGlynn J, DeCelie-Germana J, Kier C, Langfelder-Schwind E
Life (Basel). 2023; 13(7).
PMID: 37511919
PMC: 10381247.
DOI: 10.3390/life13071545.
Evolving Nutritional Needs in Cystic Fibrosis.
Frantzen T, Barsky S, LaVecchia G, Marowitz M, Wang J
Life (Basel). 2023; 13(7).
PMID: 37511806
PMC: 10381916.
DOI: 10.3390/life13071431.
Nutritional Risks in Patients Undergoing Total Pancreatectomy Islet AutoTransplantation in the POST Consortium.
Downs E, Eaton A, Witkowski P, Wijkstrom M, Walsh M, Trikudanathan G
J Gastrointest Surg. 2023; 27(9):1893-1902.
PMID: 37442881
PMC: 11335039.
DOI: 10.1007/s11605-023-05770-1.
Inhaled anti-pseudomonal antibiotics for long-term therapy in cystic fibrosis.
Smith S, Rowbotham N
Cochrane Database Syst Rev. 2022; 11:CD001021.
PMID: 36373968
PMC: 9662285.
DOI: 10.1002/14651858.CD001021.pub4.
Diet quality in cystic fibrosis - associations with patient reported outcome measures and enablers and barriers to eating a healthy diet: A protocol paper for a mixed methods study.
Greaney C, Bohan K, Tecklenborg S, Casserly B, Green J, Van de Ven P
HRB Open Res. 2022; 5:33.
PMID: 36091185
PMC: 9428499.
DOI: 10.12688/hrbopenres.13533.1.
The Exeter Activity Unlimited statement on physical activity and exercise for cystic fibrosis: methodology and results of an international, multidisciplinary, evidence-driven expert consensus.
Williams C, Barker A, Denford S, van Beurden S, Bianchim M, Caterini J
Chron Respir Dis. 2022; 19:14799731221121670.
PMID: 36068015
PMC: 9459449.
DOI: 10.1177/14799731221121670.
Update on the management of vitamins and minerals in cystic fibrosis.
Sankararaman S, Hendrix S, Schindler T
Nutr Clin Pract. 2022; 37(5):1074-1087.
PMID: 35997322
PMC: 9544449.
DOI: 10.1002/ncp.10899.
Physical activity and exercise training in cystic fibrosis.
Radtke T, Smith S, Nevitt S, Hebestreit H, Kriemler S
Cochrane Database Syst Rev. 2022; 8:CD002768.
PMID: 35943025
PMC: 9361297.
DOI: 10.1002/14651858.CD002768.pub5.
Feasibility of the A-STEP for the assessment of exercise capacity in people with cystic fibrosis.
Wilson L, Potter A, Maher C, Ellis M, Lane R, Wilson J
Pediatr Pulmonol. 2022; 57(10):2524-2532.
PMID: 35811327
PMC: 9796135.
DOI: 10.1002/ppul.26069.
Using A Work System Framework to Investigate Pharmacists' Roles in Cystic Fibrosis Management.
Abraham O, Buechel M, Gay S, Szela L, Decker C, Braun A
J Pediatr Pharmacol Ther. 2022; 27(3):270-276.
PMID: 35350161
PMC: 8939272.
DOI: 10.5863/1551-6776-27.3.270.
