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Quoted phrase not found in phrase index: "Cystic fibrosis associated meconium ileus"
Page 1
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. ...Other digestive outcomes in CF reviewed in this paper include meconium …
Cystic fibrosis (CF) is the most frequent life-limiting autosomal recessive disease in Caucasians, affecting the respiratory t …
Cystic Fibrosis is Associated with Adverse Neonatal Outcomes in Washington State, 1996-2013.
Ramos KJ, Sack CS, Mitchell KH, Goss CH, Starr JR. Ramos KJ, et al. J Pediatr. 2017 Jan;180:206-211.e1. doi: 10.1016/j.jpeds.2016.09.069. Epub 2016 Oct 25. J Pediatr. 2017. PMID: 27793338 Free PMC article.
OBJECTIVE: To determine whether cystic fibrosis (CF) is associated with adverse neonatal outcomes in a recent birth cohort in the US. ...The estimated relative risks were similar among infants born from 2006 to 2013, except SGA was no longer associated …
OBJECTIVE: To determine whether cystic fibrosis (CF) is associated with adverse neonatal outcomes in a recent birth coh …
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 …
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 fun …
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 …
Cystic fibrosis newborn screening: the importance of bloodspot sample quality.
Doull I, Course CW, Hanks RE, Southern KW, Forton JT, Thia LP, Moat SJ. Doull I, et al. Arch Dis Child. 2021 Mar;106(3):253-257. doi: 10.1136/archdischild-2020-318999. Epub 2020 Aug 28. Arch Dis Child. 2021. PMID: 32859613
OBJECTIVE: Wales has an immunoreactive trypsin (IRT)-DNA cystic fibrosis (CF) newborn screening (NBS) programme. Most CF NBS false negative cases are due to an IRT concentration below the screening threshold. ...RESULTS: Over 20 years, 673 952 infants were screened …
OBJECTIVE: Wales has an immunoreactive trypsin (IRT)-DNA cystic fibrosis (CF) newborn screening (NBS) programme. Most CF NBS f …
Clinical expression of cystic fibrosis in a large cohort of Italian siblings.
Terlizzi V, Lucarelli M, Salvatore D, Angioni A, Bisogno A, Braggion C, Buzzetti R, Carnovale V, Casciaro R, Castaldo G, Cirilli N, Collura M, Colombo C, Di Lullo AM, Elce A, Lucidi V, Madarena E, Padoan R, Quattrucci S, Raia V, Seia M, Termini L, Zarrilli F. Terlizzi V, et al. BMC Pulm Med. 2018 Dec 22;18(1):196. doi: 10.1186/s12890-018-0766-6. BMC Pulm Med. 2018. PMID: 30577776 Free PMC article.
BACKGROUND: A clinical heterogeneity was reported in patients with Cystic Fibrosis (CF) with the same CFTR genotype and between siblings with CF. ...CF related diabetes was found in 22 pairs (in 6 in both the siblings). It occurred later (median: 32.5 years) and is …
BACKGROUND: A clinical heterogeneity was reported in patients with Cystic Fibrosis (CF) with the same CFTR genotype and betwee …
Pancreatic, hepatobiliary, and gastrointestinal manifestations of children with cystic fibrosis: A 10-year experience from a tertiary care center in southern India.
Thomas L, Kumar M, Lionel BAP, Varkki S, Rebekah G. Thomas L, et al. Indian J Gastroenterol. 2022 Jun;41(3):266-272. doi: 10.1007/s12664-021-01225-0. Epub 2022 Jun 27. Indian J Gastroenterol. 2022. PMID: 35761057
OBJECTIVES: To describe the demography and spectrum of pancreatic, hepatobiliary, and gastrointestinal (GI) manifestations in children with cystic fibrosis (CF) from the Indian subcontinent. METHODS: In this retrospective study, relevant information from the databas …
OBJECTIVES: To describe the demography and spectrum of pancreatic, hepatobiliary, and gastrointestinal (GI) manifestations in children with …
Dilated and echogenic fetal bowel and postnatal outcomes: a surgical perspective. Case series and literature review.
Jackson CR, Orford J, Minutillo C, Dickinson JE. Jackson CR, et al. Eur J Pediatr Surg. 2010 May;20(3):191-3. doi: 10.1055/s-0030-1247523. Epub 2010 Feb 19. Eur J Pediatr Surg. 2010. PMID: 20175047 Review.
INTRODUCTION: Foetal dilated or echogenic bowel have been described as markers for a variety of conditions including bowel obstruction, chromosomal and infectious disorders and cystic fibrosis. We aim to describe possible surgical interventions and outcomes. ...RESU …
INTRODUCTION: Foetal dilated or echogenic bowel have been described as markers for a variety of conditions including bowel obstruction, chro …
Distal intestinal obstruction syndrome: a diagnostic and therapeutic challenge in cystic fibrosis.
Sandy NS, Massabki LHP, Gonçalves AC, Ribeiro AF, Ribeiro JD, Servidoni MFCP, Lomazi EA. Sandy NS, et al. J Pediatr (Rio J). 2020 Nov-Dec;96(6):732-740. doi: 10.1016/j.jped.2019.08.009. Epub 2019 Oct 22. J Pediatr (Rio J). 2020. PMID: 31654616 Free PMC article.
Data analyzed included age, gender, cystic fibrosis genotype, meconium ileus at birth, hydration status, pulmonary exacerbation, Pseudomonas aeruginosa colonization, pancreatic insufficiency (PI), body mass index (BMI) at the episodes, clinical manifes …
Data analyzed included age, gender, cystic fibrosis genotype, meconium ileus at birth, hydration status, pulmona …
61 results