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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1997 2
1999 4
2000 31
2001 13
2002 8
2003 14
2004 13
2005 12
2006 16
2007 17
2008 26
2009 28
2010 28
2011 28
2012 60
2013 66
2014 72
2015 68
2016 91
2017 66
2018 82
2019 79
2020 92
2021 91
2022 86
2023 93
2024 21

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1,113 results

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Page 1
Improving nutrition in cystic fibrosis: A systematic literature review.
Mielus M, Sands D, Woynarowski M. Mielus M, et al. Nutrition. 2022 Oct;102:111725. doi: 10.1016/j.nut.2022.111725. Epub 2022 May 6. Nutrition. 2022. PMID: 35816813 Free article. Review.
With increasing life expectancy of patients with cystic fibrosis (CF), gastrointestinal manifestations of the disease have been increasingly brought into focus. ...
With increasing life expectancy of patients with cystic fibrosis (CF), gastrointestinal manifestations of the disease have bee …
Physical activity and exercise training in cystic fibrosis.
Radtke T, Smith S, Nevitt SJ, Hebestreit H, Kriemler S. Radtke T, et al. Cochrane Database Syst Rev. 2022 Aug 9;8(8):CD002768. doi: 10.1002/14651858.CD002768.pub5. Cochrane Database Syst Rev. 2022. PMID: 35943025 Free PMC article. Review.
BACKGROUND: Physical activity (including exercise) may form an important part of regular care for people with cystic fibrosis (CF). This is an update of a previously published review. OBJECTIVES: To assess the effects of physical activity interventions on exercise c …
BACKGROUND: Physical activity (including exercise) may form an important part of regular care for people with cystic fibrosis …
Airway clearance techniques for cystic fibrosis: an overview of Cochrane systematic reviews.
Wilson LM, Morrison L, Robinson KA. Wilson LM, et al. Cochrane Database Syst Rev. 2019 Jan 24;1(1):CD011231. doi: 10.1002/14651858.CD011231.pub2. Cochrane Database Syst Rev. 2019. PMID: 30676656 Free PMC article.
BACKGROUND: Cystic fibrosis is a life-limiting genetic condition in which thick mucus builds up in the lungs, leading to infections, inflammation, and eventually, deterioration in lung function. ...More long-term, high-quality randomised controlled trials comparing …
BACKGROUND: Cystic fibrosis is a life-limiting genetic condition in which thick mucus builds up in the lungs, leading to infec …
Anxiety in Children with Cystic Fibrosis and Their Parents: A Systematic Review.
Kimball H, Douglas T, Sanders M, Cobham VE. Kimball H, et al. Clin Child Fam Psychol Rev. 2021 Jun;24(2):370-390. doi: 10.1007/s10567-021-00345-5. Epub 2021 Mar 4. Clin Child Fam Psychol Rev. 2021. PMID: 33660071 Review.
Individuals with cystic fibrosis (CF) are at high risk of clinically significant anxiety, which can be related to lower treatment adherence and poorer health outcomes. ...
Individuals with cystic fibrosis (CF) are at high risk of clinically significant anxiety, which can be related to lower treatm …
Physical exercise training for cystic fibrosis.
Radtke T, Nevitt SJ, Hebestreit H, Kriemler S. Radtke T, et al. Cochrane Database Syst Rev. 2017 Nov 1;11(11):CD002768. doi: 10.1002/14651858.CD002768.pub4. Cochrane Database Syst Rev. 2017. PMID: 29090734 Free PMC article. Updated. Review.
BACKGROUND: Physical exercise training may form an important part of regular care for people with cystic fibrosis. This is an update of a previously published review. ...High-quality randomised controlled trials are needed to comprehensively assess the benefits of e …
BACKGROUND: Physical exercise training may form an important part of regular care for people with cystic fibrosis. This is an …
Sleep disorders in cystic fibrosis: A systematic review and meta-analysis.
Reiter J, Gileles-Hillel A, Cohen-Cymberknoh M, Rosen D, Kerem E, Gozal D, Forno E. Reiter J, et al. Sleep Med Rev. 2020 Jun;51:101279. doi: 10.1016/j.smrv.2020.101279. Epub 2020 Feb 19. Sleep Med Rev. 2020. PMID: 32145647 Free PMC article.
Cystic fibrosis (CF) is a genetic disorder that leads to airway mucus accumulation, chronic inflammation, and recurrent respiratory infections - all likely impacting sleep. ...
Cystic fibrosis (CF) is a genetic disorder that leads to airway mucus accumulation, chronic inflammation, and recurrent respir …
Effectiveness of preconceptional and prenatal cystic fibrosis carrier screening: a systematic review.
Banzi R, Allocati E, Gerardi C, Castellani C, Rissone M, Stracuzzi M, Ferrario L, Foglia E, Mosconi P, Colombo C. Banzi R, et al. Epidemiol Prev. 2023 Jul-Oct;47(4-5):243-256. doi: 10.19191/EP23.4-5.A612.064. Epidemiol Prev. 2023. PMID: 37846447 English.
BACKGROUND: genetic testing for cystic fibrosis (CF) has been offered to people with higher risk of being carrier. ...
BACKGROUND: genetic testing for cystic fibrosis (CF) has been offered to people with higher risk of being carrier. ...
Cystic fibrosis, body composition, and health outcomes: a systematic review.
Calella P, Valerio G, Brodlie M, Donini LM, Siervo M. Calella P, et al. Nutrition. 2018 Nov;55-56:131-139. doi: 10.1016/j.nut.2018.03.052. Epub 2018 Apr 6. Nutrition. 2018. PMID: 29981489
OBJECTIVES: Patients with cystic fibrosis are characterized by an increased risk of nutrient malabsorption and inflammation, which may influence body composition. ...CONCLUSIONS: Patients with cystic fibrosis may be at an increased risk of sarcopenia a …
OBJECTIVES: Patients with cystic fibrosis are characterized by an increased risk of nutrient malabsorption and inflammation, w …
Breastfeeding in Cystic Fibrosis: A Systematic Review on Prevalence and Potential Benefits.
Colombo C, Alicandro G, Daccò V, Consales A, Mosca F, Agostoni C, Giannì ML. Colombo C, et al. Nutrients. 2021 Sep 18;13(9):3263. doi: 10.3390/nu13093263. Nutrients. 2021. PMID: 34579139 Free PMC article.
Breastfeeding (BF) is considered the normative standard of feeding for all infants. However, the impact of BF in patients with cystic fibrosis (CF) is not completely defined. Therefore, we conducted a systematic review to evaluate BF prevalence in the CF population …
Breastfeeding (BF) is considered the normative standard of feeding for all infants. However, the impact of BF in patients with cystic …
Cepacia syndrome in cystic fibrosis: A systematic review of the literature and possible new perspectives in treatment.
Daccò V, Alicandro G, Consales A, Rosazza C, Sciarrabba CS, Cariani L, Colombo C. Daccò V, et al. Pediatr Pulmonol. 2023 May;58(5):1337-1343. doi: 10.1002/ppul.26359. Epub 2023 Mar 8. Pediatr Pulmonol. 2023. PMID: 36815622 Free article. Review.
BACKGROUND: Cepacia syndrome (CS) is an acute, necrotizing pneumonia with a high mortality rate, occurring in patients with cystic fibrosis (CF) infected with Burkholderia cepacia complex (BCC). ...
BACKGROUND: Cepacia syndrome (CS) is an acute, necrotizing pneumonia with a high mortality rate, occurring in patients with cystic …
1,113 results