Cystic fibrosis diagnosis: New dilemmas for an old disorder
Author:
Publisher
Wiley
Subject
Pulmonary and Respiratory Medicine,Pediatrics, Perinatology, and Child Health
Reference15 articles.
1. Cystic fibrosis: Keeping it in the family
2. Intermediate-range sweat chloride concentration and Pseudomonas bronchitis. A cystic fibrosis variant with preservation of exocrine pancreatic function
3. Low sweat electrolytes in a patient with cystic fibrosis
4. Atypical cystic fibrosis of the pancreas with normal levels of sweat chloride and minimal pancreatic lesions
5. Relative ion permeability of normal and cystic fibrosis nasal epithelium.
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1. Diagnosis and Presentation of Cystic Fibrosis;Kendig's Disorders of the Respiratory Tract in Children;2019
2. The CFTR-Associated Ligand Arrests the Trafficking of the Mutant ΔF508 CFTR Channel in the ER Contributing to Cystic Fibrosis;Cellular Physiology and Biochemistry;2018
3. Diagnosis and Presentation of Cystic Fibrosis;Kendig & Chernickâs Disorders of the Respiratory Tract in Children;2012
4. CYSTIC FIBROSIS;Feigin and Cherry's Textbook of Pediatric Infectious Diseases;2009
5. From Resistance to Usefulness: Sociology and the Clinical Use of Genetic Tests;BioSocieties;2008-05-29
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