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Volumn 60, Issue 6, 2002, Pages 693-695

The french neonatal screening of cystic fibrosis;Mucoviscidose: Un dépistage pour toute la France

Author keywords

[No Author keywords available]

Indexed keywords

CFTR PROTEIN, HUMAN; TRANSMEMBRANE CONDUCTANCE REGULATOR;

EID: 17744417972     PISSN: 00033898     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article
Times cited : (6)

References (12)
  • 1
    • 17744372496 scopus 로고    scopus 로고
    • Early diagnosis of cystic fibrosis through neonatal screening prevents severe malnutrition and improves long-term growth
    • Wisconsin Cystic Fibrosis Neonatal Screening Study Group
    • Farrell PM, Kosorok MR, Rock MJ, et al. Early diagnosis of cystic fibrosis through neonatal screening prevents severe malnutrition and improves long-term growth. Wisconsin Cystic Fibrosis Neonatal Screening Study Group. Pediatrics 2001; 107: 1-13.
    • (2001) Pediatrics , vol.107 , pp. 1-13
    • Farrell, P.M.1    Kosorok, M.R.2    Rock, M.J.3
  • 2
    • 0034323941 scopus 로고    scopus 로고
    • Does neonatal screening of cystic fibrosis affect outcome? Comparative study of two cohorts in Britanny and Loire-Atlantique with follow-up after ten years
    • Siret D, Branger B, Storni V, et al. Does neonatal screening of cystic fibrosis affect outcome? Comparative study of two cohorts in Britanny and Loire-Atlantique with follow-up after ten years Arch Pediatr 2000; 7: 1154-62.
    • (2000) Arch Pediatr , vol.7 , pp. 1154-1162
    • Siret, D.1    Branger, B.2    Storni, V.3
  • 3
    • 0034596493 scopus 로고    scopus 로고
    • Neonatal screening for cystic fibrosis in Brittany, France: Assessment of 10 years' experience and impact on prenatal diagnosis
    • Scotet V, de Braekeleer M, Roussey M, et al. Neonatal screening for cystic fibrosis in Brittany, France: Assessment of 10 years' experience and impact on prenatal diagnosis. Lancet 2000; 356: 789-94.
    • (2000) Lancet , vol.356 , pp. 789-794
    • Scotet, V.1    De Braekeleer, M.2    Roussey, M.3
  • 4
    • 0034686221 scopus 로고    scopus 로고
    • Newborn screening for cystic fibrosis in Victoria: 10 Years' experience (1989-1998)
    • Massie RJ, Olsen M, Glazner J, Robertson CF, Francis I. Newborn screening for cystic fibrosis in Victoria: 10 Years' experience (1989-1998). Med J Aust 2000; 172: 584-7.
    • (2000) Med J Aust , vol.172 , pp. 584-587
    • Massie, R.J.1    Olsen, M.2    Glazner, J.3    Robertson, C.F.4    Francis, I.5
  • 5
    • 0030921031 scopus 로고    scopus 로고
    • Newborn screening strategy for cystic fibrosis: A field study in an area with high allelic heterogeneity
    • Castellani C, Bonizzato A, Cabrini G, Mastella G. Newborn screening strategy for cystic fibrosis: A field study in an area with high allelic heterogeneity. Acta Paediatr 1997; 86: 497-502.
    • (1997) Acta Paediatr , vol.86 , pp. 497-502
    • Castellani, C.1    Bonizzato, A.2    Cabrini, G.3    Mastella, G.4
  • 6
    • 0033860259 scopus 로고    scopus 로고
    • Spectrum of CFTR mutations in cystic fibrosis and in congenital absence of the vas deferens in France
    • Claustres M, Guittard C, Bozon D, et al. Spectrum of CFTR mutations in cystic fibrosis and in congenital absence of the vas deferens in France. Hum Mutat 2000; 16: 143-56.
    • (2000) Hum Mutat , vol.16 , pp. 143-156
    • Claustres, M.1    Guittard, C.2    Bozon, D.3
  • 8
    • 0034972954 scopus 로고    scopus 로고
    • Genetic testing for cystic fibrosis: Evaluation of the Elucigene CF20 kit in blood and buccal cells
    • Feldmann D, Guittard C, Georges MD, et al. Genetic testing for cystic fibrosis: Evaluation of the Elucigene CF20 kit in blood and buccal cells. Ann Biol Clin 2001; 59: 277-83.
    • (2001) Ann Biol Clin , vol.59 , pp. 277-283
    • Feldmann, D.1    Guittard, C.2    Georges, M.D.3
  • 9
    • 0036009317 scopus 로고    scopus 로고
    • Negative sweat test in hypertrypsinaemic infants with cystic fibrosis carrying rare CFTR mutations
    • Padoan R, Bassotti A, Seia M, Corbetta C. Negative sweat test in hypertrypsinaemic infants with cystic fibrosis carrying rare CFTR mutations. Eur J Pediatr 2002; 161: 212-5.
    • (2002) Eur J Pediatr , vol.161 , pp. 212-215
    • Padoan, R.1    Bassotti, A.2    Seia, M.3    Corbetta, C.4
  • 10
    • 0029558007 scopus 로고
    • Neonatal screening for cystic fibrosis: A comparison of two strategies for case detection in 1.2 million babies
    • Wilcken B, Wiley V, Sherry G, Bayliss U. Neonatal screening for cystic fibrosis: A comparison of two strategies for case detection in 1.2 million babies. J Pediatr 1995; 127: 965-70.
    • (1995) J Pediatr , vol.127 , pp. 965-970
    • Wilcken, B.1    Wiley, V.2    Sherry, G.3    Bayliss, U.4
  • 11
    • 0034545223 scopus 로고    scopus 로고
    • Genotype analysis and phenotypic manifestations of children with intermediate sweat chloride test results
    • Desmarquest P, Feldmann D, Tamalat A, et al. Genotype analysis and phenotypic manifestations of children with intermediate sweat chloride test results. Chest 2000; 118: 1591-7.
    • (2000) Chest , vol.118 , pp. 1591-1597
    • Desmarquest, P.1    Feldmann, D.2    Tamalat, A.3
  • 12
    • 0031900652 scopus 로고    scopus 로고
    • The diagnosis of cystic fibrosis: A consensus statement. Cystic Fibrosis Foundation Consensus Panel
    • Rosenstein BJ, Cutting GR. The diagnosis of cystic fibrosis: A consensus statement. Cystic Fibrosis Foundation Consensus Panel. J Pediatr 1998; 132: 589-95.
    • (1998) J Pediatr , vol.132 , pp. 589-595
    • Rosenstein, B.J.1    Cutting, G.R.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.