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• W2014873146 abstract "Journal of Inherited Metabolic DiseaseVolume 26, Issue 8 p. 725-727 Commentary Newborn screening for cystic fibrosis: Science, legislation, and human values R. J. Pollitt, Corresponding Author R. J. Pollitt [email protected] The Children's Hospital, Sheffield, S10 2TH UK[email protected]Search for more papers by this author R. J. Pollitt, Corresponding Author R. J. Pollitt [email protected] The Children's Hospital, Sheffield, S10 2TH UK[email protected]Search for more papers by this author First published: 01 December 2003 https://doi.org/10.1023/B:BOLI.0000009975.91855.ccCitations: 2 This revised version was published online in August 2006 with corrections to the Cover Date. AboutPDF ToolsRequest permissionExport citationAdd to favoritesTrack citation ShareShare Give accessShare full text accessShare full-text accessPlease review our Terms and Conditions of Use and check box below to share full-text version of article.I have read and accept the Wiley Online Library Terms and Conditions of UseShareable LinkUse the link below to share a full-text version of this article with your friends and colleagues. Learn more.Copy URL Share a linkShare onEmailFacebookTwitterLinkedInRedditWechat REFERENCES 1 Anonymous (2001) Screening brief: Neonatal screening for cystic fibrosis. J Med Screen, 8: 51, . 2Boyne J, Evans S, Pollitt RJ, Taylor CJ, Dalton A (2000) Many AF508 heterozygote neonates with transient hypertrypsinaemia have a second, mild CFTR mutation. J Med Genet, 37: 543–547, . 3Dhondt JL, Farriaux JP, Briard ML, Boschetti R, Fr6zal J (1993) Results of pilot screening activities in the French neonatal screening program cystic fibrosis, congenital adrenal hyperplasia and sickle cell disease. Screening, 2: 87–89, . 4Eaton RB, Comeau AM, Zytkovicz TH, Larson C (2002) Newborn screening: New developments in a proven field. Clin Lab Sci, 15: 239–244. 5Farriaux JP, Vidailhet M, Briard ML, Belot V, Dhondt JL. (2003) Neonatal screening for cystic fibrosis: France rises to the challenge. J Inherit Metab Dis, 26: 000–000, . 6McCormick J, Green MW, Mehta G, Culross F, Mehta A (2002) Demographics of the UK cystic fibrosis population: Implications for neonatal screening. Eur J Hum Genet, 10: 583–590, . 7Merelle ME, Huisman J, Alderden-van der Vecht A et al (2003) Early versus late diagnosis: psychological impact on parents of children with cystic fibrosis. Pediatrics, 111: 346–500, . 8Pollitt RJ, Dalton A, Evans S, Hughes HN, Curtis D (1997) Neonatal screening for cystic fibrosis in the Trent region (UK): two-stage immunoreactive trypsin screening compared with a three-stage protocol with DNA analysis as an intermediate step. J Med Screen, 4: 23–28. 9Ranieri E, Ryall RG, Morris CP et al (1991) Neonatal screening strategy for cystic fibrosis using immunoreactive trypsinogen and direct gene analysis. Br Med J, 302: 1237–1240, . 10Rosenstein BJ (2003) Non-classical cystic fibrosis: a clinical conundrum. Pediatr Pulmonol, 36: 10–12, . 11Travert G (1988) Analyse de l'exp6rience mondiale de d6pistage neonatal de la mucoviscidose par dosage de la trypsine immunoreactive sanguine. In: G Travert, ed. Mucoviscidose. Dtpistage neonatal et prise en charge precose., University Caen, 1–23. 12Wilfond B, Rosenberg LS (2002) Ethical issues in cystic fibrosis screening: from data to public health policy. Curr Opin Pulm Med, 8: 529–553, . Citing Literature Volume26, Issue8December 2003Pages 725-727 ReferencesRelatedInformation" @default.
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