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Uncertainty in the diagnosis of cystic fibrosis: Possible role of in vivo nasal potential difference measurements

  • Published:1998-04 Issue:4 Volume:132 Page:596-599
  • ISSN:0022-3476
  • Container-title:The Journal of Pediatrics
  • language:en
  • Short-container-title:The Journal of Pediatrics

Author:

Wilson David C.,Ellis Lynda,Zielenski Julian,Corey Mary,Ip Wan F.,Tsui Lap-Chee,Tullis Elizabeth,Knowles Michael R.,Durie Peter R.

Publisher

Elsevier BV

Subject

Pediatrics, Perinatology, and Child Health

Reference16 articles.

1. Cystic fibrosis;Welsh,1995

2. Identification of the cystic fibrosis gene: cloning and characterization of complementary DNA;Riordan;Science,1989

3. A test for concentration of electrolytes in sweat in cystic fibrosis of the pancreas utilizing pilocarpine by iontophoresis;Gibson;Pediatrics,1959

4. The relation between genotype and phenotype in cystic fibrosis: analysis of the most common mutation (ΔF508);Kerem;N Engl J Med,1990

5. The bentiromide test using plasma p-aminobenzoic acid for diagnosing pancreatic insufficiency in young children;Laufer;Gastroenterology,1991

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1. Cystic Fibrosis;Airway diseases;2023

2. Cystic fibrosis;Biochemical and Molecular Basis of Pediatric Disease;2021

3. Cystic Fibrosis;Emery and Rimoin's Principles and Practice of Medical Genetics and Genomics;2020

4. Measurement of ion fluxes across epithelia;Progress in Biophysics and Molecular Biology;2017-08

5. Relationships among CFTR expression, HCO3− secretion, and host defense may inform gene- and cell-based cystic fibrosis therapies;Proceedings of the National Academy of Sciences;2016-04-25
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