Nasal potential difference in suspected cystic fibrosis patients with 5T polymorphism-Reference-Cited by-同舟云学术

Nasal potential difference in suspected cystic fibrosis patients with 5T polymorphism

Published:2020-07 Issue:4 Volume:19 Page:627-631
ISSN:1569-1993
Container-title:Journal of Cystic Fibrosis
language:en
Short-container-title:Journal of Cystic Fibrosis

Author:

Aalbers Bente L.,Yaakov Yasmin,Derichs Nico,Simmonds Nicholas J.,De Wachter Elke,Melotti Paola,De Boeck Kris,Leal Teresinha,Tümmler Burkhart,Wilschanski Michael,Bronsveld Inez

Funder

NCFS

Publisher

Elsevier BV

Subject

Pulmonary and Respiratory Medicine,Pediatrics, Perinatology and Child Health

Reference30 articles.

1. Cystic fibrosis;Welsh;Sci Am,1995

2. Guidelines for diagnosis of cystic fibrosis in newborns through older adults: cystic fibrosis foundation consensus report;Farrell;J Pediatr,2008

3. CFTR cl channel function in native human colon correlates with the genotype and phenotype in cystic fibrosis;Hirtz;Gastroenterology,2004

4. Lung disease associated with the IVS8 5T allele of the CFTR gene;Noone;Am J Respir Crit Care Med,2000

5. Extensive posttranscriptional deletion of the coding sequences for part of nucleotide-binding fold 1 in respiratory epithelial mRNA transcripts of the cystic fibrosis transmembrane conductance regulator gene is not associated with the clinical manifestations of cystic fibrosis.

Cited by 10 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Recurrent Wheezing in a Child: Unraveling Atypical Presentations of Cystic Fibrosis and Polymorphisms: A Case Report;Current Respiratory Medicine Reviews;2024-11

2. Diagnostic challenges in CFTR-related metabolic syndrome: Where the guidelines fall short;Paediatric Respiratory Reviews;2023-08

3. Diagnosing Cystic Fibrosis in Adults;Seminars in Respiratory and Critical Care Medicine;2023-01-09

4. ECFS standards of care on CFTR-related disorders: Diagnostic criteria of CFTR dysfunction;Journal of Cystic Fibrosis;2022-11

5. ECFS standards of care on CFTR-related disorders: Updated diagnostic criteria;Journal of Cystic Fibrosis;2022-11