Diagnosis of CF despite normal or borderline sweat chloride
Author:
Publisher
Elsevier BV
Subject
Pulmonary and Respiratory Medicine,Pediatrics, Perinatology and Child Health
Reference17 articles.
1. A novel mutation in the CF gene in patients with pulmonary disease but normal sweat chloride concentrations;Highsmith;N Engl J Med,1994
2. Sweat testing for the diagnosis of cystic fibrosis: Practical considerations;Legrys;J Pediatr,1996
3. Cooperative study comparing three methods of performing sweat tests to diagnose cystic fibrosis;Denning;Pediatrics,1980
4. Incidence and implications of false negative sweat test reports in patients with cystic fibrosis;Legrys;Pediatr Pulmonol,1988
5. Variation of sweat sodium and chloride with age in cystic fibrosis and normal populations: further investigations in equivocal cases;Kirk;Ann Clin Biochem,1992
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1. Comparison between Gibson–Cooke and Macroduct Methods in the Cystic Fibrosis Neonatal Screening Program and in Subjects Who Are Cystic Fibrosis Screen-Positive with an Inconclusive Diagnosis;International Journal of Neonatal Screening;2023-07-25
2. Quality of sweat test (ST) based on the proportion of sweat sodium (Na) and sweat chloride (Cl) as diagnostic parameter of cystic fibrosis: are we on the right way?;Diagnostic Pathology;2016-10-26
3. Sweat conductivity: An accurate diagnostic test for cystic fibrosis?;Journal of Cystic Fibrosis;2014-09
4. Comparison between classic Gibson and Cooke technique and sweat conductivity test in patients with and without cystic fibrosis;Jornal de Pediatria;2010-02-10
5. Overview;Pediatric Respiratory Medicine;2008
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