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Quoted phrase not found in phrase index: "Cystic fibrosis associated meconium ileus"
Page 1
Cystic fibrosis-associated liver disease in children.
Wasuwanich P, Karnsakul W. Wasuwanich P, et al. Minerva Pediatr. 2020 Oct;72(5):440-447. doi: 10.23736/S0026-4946.20.05895-8. Epub 2020 May 15. Minerva Pediatr. 2020. PMID: 32418413 Review.
As improvements in nutritional and pulmonary care increase the life expectancy of cystic fibrosis (CF) patients, CF-associated liver disease (CFLD) is emerging as a cause of mortality. ...Having the SERPINA1 Z allele, a history of pancreatic insufficiency, a …
As improvements in nutritional and pulmonary care increase the life expectancy of cystic fibrosis (CF) patients, CF-associa
Digestive outcomes in Cystic fibrosis.
Ley D, Turck D. Ley D, et al. Best Pract Res Clin Gastroenterol. 2022 Feb-Mar;56-57:101788. doi: 10.1016/j.bpg.2022.101788. Epub 2022 Feb 24. Best Pract Res Clin Gastroenterol. 2022. PMID: 35331400 Review.
Cystic fibrosis (CF) is the most frequent life-limiting autosomal recessive disease in Caucasians, affecting the respiratory tract, but also the pancreas, gut, and hepatobiliary tract. CF is caused by variants in the Cystic Fibrosis Transmembrane condu
Cystic fibrosis (CF) is the most frequent life-limiting autosomal recessive disease in Caucasians, affecting the respiratory t
Clinical and genetic features of cystic fibrosis in Japan.
Kozawa Y, Yamamoto A, Nakakuki M, Fujiki K, Kondo S, Okada T, Fukuyasu T, Yamaguchi M, Taniguchi I, Nomura N, Liu L, Higuchi M, Niwa E, Sohma Y, Naruse S, Takeyama Y, Ishiguro H. Kozawa Y, et al. J Hum Genet. 2023 Oct;68(10):671-680. doi: 10.1038/s10038-023-01160-2. Epub 2023 May 22. J Hum Genet. 2023. PMID: 37217688
Cystic fibrosis (CF) is an autosomal recessive disease caused by pathogenic variants in CF transmembrane conductance regulator (CFTR). ...CF patients in Japan were found to have chronic sinopulmonary disease (85.6%), exocrine pancreatic insufficiency (66.7%), mec
Cystic fibrosis (CF) is an autosomal recessive disease caused by pathogenic variants in CF transmembrane conductance regulator
Cystic fibrosis and fat malabsorption: Pathophysiology of the cystic fibrosis gastrointestinal tract and the impact of highly effective CFTR modulator therapy.
McDonald CM, Reid EK, Pohl JF, Yuzyuk TK, Padula LM, Vavrina K, Altman K. McDonald CM, et al. Nutr Clin Pract. 2024 Apr;39 Suppl 1:S57-S77. doi: 10.1002/ncp.11122. Nutr Clin Pract. 2024. PMID: 38429959 Review.
Cystic fibrosis (CF) is a progressive, genetic, multi-organ disease affecting the respiratory, digestive, endocrine, and reproductive systems. ...Additionally, other factors can cause or worsen fat malabsorption, including the potential for short gut syndrome with a
Cystic fibrosis (CF) is a progressive, genetic, multi-organ disease affecting the respiratory, digestive, endocrine, and repro
Geographic distribution and phenotype of European people with cystic fibrosis carrying A1006E mutation.
Mondejar-Lopez P, Zolin A, Garcia-Marcos PW, Pastor-Vivero MD, Rosa-Silvestre M, de Asis Sanchez-Martinez F, Salvatore D, Cimino G, Majo F, Sole-Jover A, Asensio de la Cruz O, Calderazzo MA, Pizzamiglio G, Castillo-Corullon S, Alvarez-Fernandez A, Gartner S, Padoan R, Carnovale V, Salvatore M, Moya-Quiles MR, Orenti A, Glover G, Sanchez-Solis M. Mondejar-Lopez P, et al. Respir Med. 2022 Feb;192:106736. doi: 10.1016/j.rmed.2022.106736. Epub 2022 Jan 6. Respir Med. 2022. PMID: 35032736 Free article.
BACKGROUND: A1006E is a Cystic Fibrosis (CF) mutation that is still not widely known. We report phenotypic features and geographic distribution of the largest cohort of people with CF (pwCF) carrying A1006E to date. ...Compared to F508del homozygous, A1006E-pwCF wer …
BACKGROUND: A1006E is a Cystic Fibrosis (CF) mutation that is still not widely known. We report phenotypic features and geogra …
Cholestasis and meconium ileus in infants with cystic fibrosis and their clinical outcomes.
Leeuwen L, Magoffin AK, Fitzgerald DA, Cipolli M, Gaskin KJ. Leeuwen L, et al. Arch Dis Child. 2014 May;99(5):443-7. doi: 10.1136/archdischild-2013-304159. Epub 2014 Jan 16. Arch Dis Child. 2014. PMID: 24436365
OBJECTIVE: To identify the incidence and outcomes of cholestasis and meconium ileus (MI) in infants with cystic fibrosis (CF). DESIGN: Retrospective cohort study. ...MAIN OUTCOME MEASUREMENTS: (1) incidence of cholestasis, (2) identification of risk fa …
OBJECTIVE: To identify the incidence and outcomes of cholestasis and meconium ileus (MI) in infants with cystic fibr
A review of pathophysiology and management of fetuses and neonates with meconium ileus for the pediatric surgeon.
Carlyle BE, Borowitz DS, Glick PL. Carlyle BE, et al. J Pediatr Surg. 2012 Apr;47(4):772-81. doi: 10.1016/j.jpedsurg.2012.02.019. J Pediatr Surg. 2012. PMID: 22498395 Review.
PURPOSE: Meconium ileus (MI) is the earliest clinical manifestation of cystic fibrosis (CF), occurring in up to 20% of patients with CF. ...METHODS: We identified areas of interest including pathophysiology, prenatal diagnosis, nonoperative and operati …
PURPOSE: Meconium ileus (MI) is the earliest clinical manifestation of cystic fibrosis (CF), occurring in up to …
The success of the Cystic Fibrosis Registry of Turkey for improvement of patient care.
Asfuroglu P, Sismanlar Eyuboglu T, Aslan AT, Gursoy TR, Emiralioglu N, Yalcin E, Kiper N, Sen V, Sen HS, Altintas DU, Ozcan D, Kilinc AA, Cokugras H, Baskan AK, Yazan H, Erenberk U, Dogan G, Unal G, Yilmaz AI, Keskin O, Arik E, Kucukosmanoglu E, Irmak I, Damadoglu E, Ozturk GK, Gulen F, Basaran AE, Bingol A, Cekic S, Sapan N, Kilic G, Harmanci K, Kose M, Ozdemir A, Tugcu GD, Polat SE, Hangul M, Ozcan G, Aydin ZGG, Yuksel H, Topal E, Ozdogan S, Caltepe G, Suleyman A, Can D, Ekren PK, Bal CM, Kilic M, Cinel G, Cobanoglu N, Pekcan S, Cakir E, Ozcelik U, Dogru D. Asfuroglu P, et al. Pediatr Pulmonol. 2022 May;57(5):1245-1252. doi: 10.1002/ppul.25852. Epub 2022 Feb 11. Pediatr Pulmonol. 2022. PMID: 35102722
BACKGROUND: Cystic fibrosis (CF) registries play an essential role in improving disease outcomes of people with CF. ...METHODS: Age at diagnosis, current age, sex, z-scores of weight, height and body mass index (BMI), neonatal screening results, pulmonary function t …
BACKGROUND: Cystic fibrosis (CF) registries play an essential role in improving disease outcomes of people with CF. ...METHODS …
Incidence and risk factors of cancer in individuals with cystic fibrosis in the UK; a case-control study.
Archangelidi O, Cullinan P, Simmonds NJ, Mentzakis E, Peckham D, Bilton D, Carr SB. Archangelidi O, et al. J Cyst Fibros. 2022 Mar;21(2):302-308. doi: 10.1016/j.jcf.2021.07.004. Epub 2021 Aug 1. J Cyst Fibros. 2022. PMID: 34348871 Free article.
To assess cancer incidence in the UK cystic fibrosis (CF) population and determine the associated risk factors, we undertook a nested case-control study of patients with CF, registered with the UK CF Registry. ...Conditional logistic regressions were adjusted …
To assess cancer incidence in the UK cystic fibrosis (CF) population and determine the associated risk factors, we unde …
77 results