Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My NCBI Filters

Results by year

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

Year Number of Results
2001 2
2002 1
2004 1
2006 1
2007 1
2008 2
2009 2
2010 1
2011 2
2012 8
2013 14
2014 7
2015 9
2016 9
2017 8
2018 12
2019 8
2020 19
2021 10
2022 18
2023 9
2024 6

Text availability

Article attribute

Article type

Publication date

Search Results

137 results

Results by year

Filters applied: . Clear all
Page 1
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 …
Bronchiectasis.
Magis-Escurra C, Reijers MH. Magis-Escurra C, et al. BMJ Clin Evid. 2015 Feb 25;2015:1507. BMJ Clin Evid. 2015. PMID: 25715965 Free PMC article. Review.
It can be associated with primary ciliary dyskinesia, primary immunodeficiencies, certain systemic diseases such as inflammatory bowel disease and rheumatoid arthritis, and foreign body inhalation. Bronchiectasis can be due to cystic fibrosis but this is excluded fr …
It can be associated with primary ciliary dyskinesia, primary immunodeficiencies, certain systemic diseases such as inflammatory bowel disea …
Surgery for nasal polyposis in cystic fibrosis.
Almeida PRL, Person OC, Puga ME, Atallah ÁN, Trevisani VF. Almeida PRL, et al. Cochrane Database Syst Rev. 2023 Dec 8;12(12):CD014084. doi: 10.1002/14651858.CD014084.pub2. Cochrane Database Syst Rev. 2023. PMID: 38063253 Review.
BACKGROUND: Cystic fibrosis (CF) is a life-shortening, autosomal recessive disease that leads to abnormal electrolyte concentration in exocrine secretions. ...AUTHORS' CONCLUSIONS: Very low-certainty evidence means we are not certain if endoscopic sinus surgery
BACKGROUND: Cystic fibrosis (CF) is a life-shortening, autosomal recessive disease that leads to abnormal electrolyte concentr …
Laparoscopic surgery in patients with cystic fibrosis: A systematic review.
El Boghdady M, Ewalds-Kvist BM. El Boghdady M, et al. Asian J Endosc Surg. 2021 Jul;14(3):327-334. doi: 10.1111/ases.12874. Epub 2020 Oct 6. Asian J Endosc Surg. 2021. PMID: 33025750
INTRODUCTION: Laparoscopic surgery may be advantageous for cystic fibrosis (CF) patients because it leads to fewer complications than open surgery. ...A literature search was performed using PubMed/MEDLINE, ScienceDirect, EMBASE, and Google Scholar, wi …
INTRODUCTION: Laparoscopic surgery may be advantageous for cystic fibrosis (CF) patients because it leads to fewer comp …
Systematic Review of the Prevalence of Kidney Stones in Cystic Fibrosis.
Moryousef J, Kwong J, Kishibe T, Ordon M. Moryousef J, et al. J Endourol. 2021 Nov;35(11):1693-1700. doi: 10.1089/end.2021.0151. Epub 2021 Sep 17. J Endourol. 2021. PMID: 33906435 Review.
Purpose: To investigate the prevalence of urolithiasis in cystic fibrosis (CF) and to summarize the available clinical features within this unique population. ...There was no apparent sex difference, with a female to male ratio of 1:1. Surgical intervention w …
Purpose: To investigate the prevalence of urolithiasis in cystic fibrosis (CF) and to summarize the available clinical feature …
Newly Discovered Cutting-Edge Triple Combination Cystic Fibrosis Therapy: A Systematic Review.
Dawood SN, Rabih AM, Niaj A, Raman A, Uprety M, Calero MJ, Villanueva MRB, Joshaghani N, Villa N, Badla O, Goit R, Saddik SE, Mohammed L. Dawood SN, et al. Cureus. 2022 Sep 20;14(9):e29359. doi: 10.7759/cureus.29359. eCollection 2022 Sep. Cureus. 2022. PMID: 36284811 Free PMC article. Review.
A cystic fibrosis (CF) transmembrane conductor regulator (CFTR) gene modulating triple therapy combining elexacaftor-tezacaftor-ivacaftor (Trikafta) has been recently discovered. ...
A cystic fibrosis (CF) transmembrane conductor regulator (CFTR) gene modulating triple therapy combining elexacaftor-tezacafto …
Bronchiectasis.
Ten Hacken NH, Kerstjens HA. Ten Hacken NH, et al. BMJ Clin Evid. 2011 Aug 16;2011:1507. BMJ Clin Evid. 2011. PMID: 21846412 Free PMC article. Review.
Bronchiectasis may cause signs of chronic obstructive pulmonary disease. It can also be associated with cystic fibrosis and other congenital disorders, foreign body inhalation, and other causes of lung damage. METHODS AND OUTCOMES: We conducted a systematic review a …
Bronchiectasis may cause signs of chronic obstructive pulmonary disease. It can also be associated with cystic fibrosis and ot …
Role of Salivary Biomarkers in Cystic Fibrosis: A Systematic Review.
Almeslet A, Alnamlah S, Alanzan L, Aldriwesh R, AlWehaiby S. Almeslet A, et al. Biomed Res Int. 2022 Jan 19;2022:5818840. doi: 10.1155/2022/5818840. eCollection 2022. Biomed Res Int. 2022. PMID: 35097122 Free PMC article. Review.
BACKGROUND: Saliva biomarkers could be easily used as a noninvasive alternative tool for diagnosing cystic fibrosis (CF) disease. In this study, the significance of changes in salivary compositions in patients with CF was systematically reviewed. ...CONCLUSION: Alte …
BACKGROUND: Saliva biomarkers could be easily used as a noninvasive alternative tool for diagnosing cystic fibrosis (CF) disea …
Endoscopic sinus surgery in patients with cystic fibrosis: a systematic review and meta-analysis of pulmonary function.
Macdonald KI, Gipsman A, Magit A, Fandino M, Massoud E, Witterick IJ, Hong P. Macdonald KI, et al. Rhinology. 2012 Dec;50(4):360-9. doi: 10.4193/Rhino.11.271. Rhinology. 2012. PMID: 23181249 Review.
INTRODUCTION: The role of endoscopic sinus surgery (ESS) in patients with cystic fibrosis (CF) is not clearly defined. ...METHODS: A systematic review was performed using the keywords 'sinusitis,' 'sinus surgery,' 'nasal polyps' and 'cystic f
INTRODUCTION: The role of endoscopic sinus surgery (ESS) in patients with cystic fibrosis (CF) is not clearly defined. …
Bronchiectasis.
ten Hacken N, Kerstjens H, Postma D. ten Hacken N, et al. BMJ Clin Evid. 2008 Jan 2;2008:1507. BMJ Clin Evid. 2008. PMID: 19450337 Free PMC article. Review.
Bronchiectasis may cause signs of chronic obstructive pulmonary disease. It can also be associated with cystic fibrosis and other congenital disorders, foreign body inhalation, and other causes of lung damage. METHODS AND OUTCOMES: We conducted a systematic review a …
Bronchiectasis may cause signs of chronic obstructive pulmonary disease. It can also be associated with cystic fibrosis and ot …
137 results