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2018 1
2019 1
2020 89
2021 2
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Sexual and reproductive health in cystic fibrosis.
Frayman KB, Chin M, Sawyer SM, Bell SC. Frayman KB, et al. Curr Opin Pulm Med. 2020 Nov;26(6):685-695. doi: 10.1097/MCP.0000000000000731. Curr Opin Pulm Med. 2020. PMID: 32941352
This review aims to describe advances in cystic fibrosis-related SRH and highlight optimal practices. RECENT FINDINGS: Recent publications suggest that people with cystic fibrosis follow a similar trajectory of sexual development and activity as their …
This review aims to describe advances in cystic fibrosis-related SRH and highlight optimal practices. RECENT FINDINGS: Recent …
Treatment of pulmonary exacerbations in cystic fibrosis.
Ng C, Nadig T, Smyth AR, Flume P. Ng C, et al. Curr Opin Pulm Med. 2020 Nov;26(6):679-684. doi: 10.1097/MCP.0000000000000730. Curr Opin Pulm Med. 2020. PMID: 32890021
Chronic cystic fibrosis therapies have been shown to reduce pulmonary exacerbations. In the era of new CFTR (cystic fibrosis transmembrane conductance regulator) modulator therapies, the number of pulmonary exacerbations are expected to be even fewer. …
Chronic cystic fibrosis therapies have been shown to reduce pulmonary exacerbations. In the era of new CFTR (cystic
The role of essential fatty acids in cystic fibrosis and normalizing effect of fenretinide.
Garić D, Dumut DC, Shah J, De Sanctis JB, Radzioch D. Garić D, et al. Cell Mol Life Sci. 2020 Nov;77(21):4255-4267. doi: 10.1007/s00018-020-03530-x. Epub 2020 May 11. Cell Mol Life Sci. 2020. PMID: 32394023 Review.
Cystic fibrosis (CF) is the most common autosomal-recessive disease in Caucasians caused by mutations in the CF transmembrane regulator (CFTR) gene. ...
Cystic fibrosis (CF) is the most common autosomal-recessive disease in Caucasians caused by mutations in the CF transmembrane
Dysregulated signalling pathways in innate immune cells with cystic fibrosis mutations.
Lara-Reyna S, Holbrook J, Jarosz-Griffiths HH, Peckham D, McDermott MF. Lara-Reyna S, et al. Cell Mol Life Sci. 2020 Nov;77(22):4485-4503. doi: 10.1007/s00018-020-03540-9. Epub 2020 May 4. Cell Mol Life Sci. 2020. PMID: 32367193 Free article. Review.
Cystic fibrosis (CF) is one of the most common life-limiting recessive genetic disorders in Caucasians, caused by mutations in the cystic fibrosis transmembrane conductance regulator (CFTR). ...
Cystic fibrosis (CF) is one of the most common life-limiting recessive genetic disorders in Caucasians, caused by mutations in
Monitoring early stage lung disease in cystic fibrosis.
Nissenbaum C, Davies G, Horsley A, Davies JC. Nissenbaum C, et al. Curr Opin Pulm Med. 2020 Nov;26(6):671-678. doi: 10.1097/MCP.0000000000000732. Curr Opin Pulm Med. 2020. PMID: 32925367
As diagnosis happens earlier and conventional management improves, we are seeing larger proportions of people with cystic fibrosis (CF) in adolescence and even adulthood with well preserved lung health. The availability of highly effective cystic fibrosis
As diagnosis happens earlier and conventional management improves, we are seeing larger proportions of people with cystic fibrosis
Selectively targeting key inflammatory pathways in cystic fibrosis.
Costantini C, Puccetti M, Pariano M, Renga G, Stincardini C, D'Onofrio F, Bellet MM, Cellini B, Giovagnoli S, Romani L. Costantini C, et al. Eur J Med Chem. 2020 Nov 15;206:112717. doi: 10.1016/j.ejmech.2020.112717. Epub 2020 Aug 9. Eur J Med Chem. 2020. PMID: 32823008
Cystic fibrosis (CF) is a rare genetic disorder caused by a defect in the ion channel Cystic Fibrosis Transmembrane conductance Regulator (CFTR), resulting in ionic imbalance of surface fluid. ...
Cystic fibrosis (CF) is a rare genetic disorder caused by a defect in the ion channel Cystic Fibrosis Transmembr
Pilot study for cystic fibrosis neonatal screening: the Cuban experience.
Castells EM, Sánchez A, Frómeta A, Mokdse Y, Ozunas N, Licourt T, Arteaga AL, Silva E, Collazo T, Rodríguez F, Martín O, Espinosa M, Del Río L, Pérez PL, Morejón G, Almira C, Núñez Z, Melchor A, González EC. Castells EM, et al. Clin Chem Lab Med. 2020 Oct 25;58(11):1857-1864. doi: 10.1515/cclm-2020-0037. Clin Chem Lab Med. 2020. PMID: 32352395
Background In Cuba, no screening program for cystic fibrosis (CF) has been implemented yet. The ultramicro enzyme-linked immunosorbent assay (UMELISA)TIR NEONATAL has been developed for the measurement of immunoreactive trypsin (IRT) in dried blood spots on filter p …
Background In Cuba, no screening program for cystic fibrosis (CF) has been implemented yet. The ultramicro enzyme-linked immun …
Explaining the Sex Effect on Survival in Cystic Fibrosis: a Joint Modeling Study of UK Registry Data.
Taylor-Robinson D, Schlüter DK, Diggle PJ, Barrett JK. Taylor-Robinson D, et al. Epidemiology. 2020 Nov;31(6):872-879. doi: 10.1097/EDE.0000000000001248. Epidemiology. 2020. PMID: 32841985 Free PMC article.
METHODS: This study analyzes data between 1996 and 2015 from the longitudinal registry study of the UK Cystic Fibrosis Registry. ...CONCLUSIONS: We estimate that about 37% of the association of sex on survival in cystic fibrosis is mediated through lun …
METHODS: This study analyzes data between 1996 and 2015 from the longitudinal registry study of the UK Cystic Fibrosis Registr …
Editorial: The changing landscape of cystic fibrosis: new therapies, challenges and a global pandemic.
Barry PJ, Plant BJ. Barry PJ, et al. Curr Opin Pulm Med. 2020 Nov;26(6):668-670. doi: 10.1097/MCP.0000000000000734. Curr Opin Pulm Med. 2020. PMID: 32941353 No abstract available.
Early pathogenesis of cystic fibrosis gallbladder disease in a porcine model.
Zarei K, Stroik MR, Gansemer ND, Thurman AL, Ostedgaard LS, Ernst SE, Thornell IM, Powers LS, Pezzulo AA, Meyerholz DK, Stoltz DA. Zarei K, et al. Lab Invest. 2020 Nov;100(11):1388-1399. doi: 10.1038/s41374-020-0474-8. Epub 2020 Jul 27. Lab Invest. 2020. PMID: 32719544 Free article.
Hepatobiliary disease causes significant morbidity in people with cystic fibrosis (CF), yet this problem remains understudied. ...
Hepatobiliary disease causes significant morbidity in people with cystic fibrosis (CF), yet this problem remains understudied. …
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