A European consensus for the evaluation and management of infants with an equivocal diagnosis following newborn screening for cystic fibrosis.
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A Munck | K G Brownlee | C Castellani | C. Castellani | I. Sermet | M. Schwarz | A. Munck | K. Southern | J. Craig | K W Southern | K. Brownlee | S J Mayell | J V Craig | I Sermet | M J Schwarz | S. Mayell | Balascakova Miroslava | Gabriel Bellon | Hopital Debrousse | France Brownlee Lyon | Keith | Elinor Burrows | Andrew Bush | De Boeck | Kristiane | John Dodge | Macek Milan | Quattrucci Serena | Reid Alastair | Renner Sabine | Southern Kevin | Schwarz Martin | Taccetti Giovanni | Weller Peter | Wilschanski Michael
[1] J. Dankert-Roelse,et al. Newborn screening for cystic fibrosis. , 2009, The Cochrane database of systematic reviews.
[2] K. Southern. Newborn screening for cystic fibrosis: the practical implications. , 2004, Journal of the Royal Society of Medicine.
[3] Xavier Estivill,et al. Variation in a repeat sequence determines whether a common variant of the cystic fibrosis transmembrane conductance regulator gene is pathogenic or benign. , 2004, American journal of human genetics.
[4] P. Farrell. Is newborn screening for cystic fibrosis a basic human right? , 2008, Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society.
[5] D. Spiegelhalter,et al. Consensus development methods, and their use in clinical guideline development. , 1998, Health technology assessment.
[6] C. Castellani,et al. Cystic fibrosis carriers have higher neonatal immunoreactive trypsinogen values than non‐carriers , 2005, American journal of medical genetics. Part A.
[7] K. Webb,et al. Delayed diagnosis of cystic fibrosis associated with R117H on a background of 7T polythymidine tract at intron 8. , 2006, Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society.
[8] R. Parad,et al. Sweat testing infants detected by cystic fibrosis newborn screening. , 2005, The Journal of pediatrics.
[9] JeanetteR. Crossle,et al. DRIED-BLOOD SPOT SCREENING FOR CYSTIC FIBROSIS IN THE NEWBORN , 1979, The Lancet.
[10] C. Férec,et al. Neonatal screening of cystic fibrosis: diagnostic problems with CFTR mild mutations , 2007, Journal of Inherited Metabolic Disease.
[11] P. V. van Asperen,et al. Pancreatic function and extended mutation analysis in DeltaF508 heterozygous infants with an elevated immunoreactive trypsinogen but normal sweat electrolyte levels. , 2000, The Journal of pediatrics.
[12] J. Yankaskas,et al. Diagnostic sweat testing: the Cystic Fibrosis Foundation guidelines. , 2007, The Journal of pediatrics.
[13] C. Castellani,et al. A survey of newborn screening for cystic fibrosis in Europe. , 2007, Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society.
[14] C. Dezateux,et al. Newborn screening for cystic fibrosis (Cochrane Review) , 2001 .
[15] M. Goossens,et al. Polyvariant mutant cystic fibrosis transmembrane conductance regulator genes. The polymorphic (Tg)m locus explains the partial penetrance of the T5 polymorphism as a disease mutation. , 1998, The Journal of clinical investigation.
[16] M. Laughon,et al. Sweat‐testing in preterm and full‐term infants less than 6 weeks of age , 2005, Pediatric pulmonology.
[17] B. Kerem,et al. Consensus on the Use and Interpretation of Cystic Fibrosis Mutation Analysis in Clinical Practice , 2022 .