Sweat Testing Infants Detected by Cystic Fibrosis Newborn Screening
- 30 September 2005
- journal article
- research article
- Published by Elsevier in The Journal of Pediatrics
- Vol. 147 (3) , S69-S72
- https://doi.org/10.1016/j.jpeds.2005.08.015
Abstract
No abstract availableKeywords
This publication has 6 references indexed in Scilit:
- Diagnostic dilemmas resulting from the immunoreactive trypsinogen/DNA cystic fibrosis newborn screening algorithmThe Journal of Pediatrics, 2005
- Population-Based Newborn Screening for Genetic Disorders When Multiple Mutation DNA Testing Is Incorporated: A Cystic Fibrosis Newborn Screening Model Demonstrating Increased Sensitivity but More Carrier DetectionsPublished by American Academy of Pediatrics (AAP) ,2004
- Newborn Screening for Cystic FibrosisPediatric Annals, 2003
- Mutations of the Cystic Fibrosis Gene and Intermediate Sweat Chloride Levels in ChildrenAmerican Journal of Respiratory and Critical Care Medicine, 2002
- Negative sweat test in hypertrypsinaemic infants with cystic fibrosis carrying rare CFTR mutations.European Journal of Pediatrics, 2002
- Nutritional Benefits of Neonatal Screening for Cystic FibrosisNew England Journal of Medicine, 1997