Cystic fibrosis and survival to 40 years: a study of cystic fibrosis transmembrane conductance regulator function-Reference-Cited by-同舟云学术

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Cystic fibrosis and survival to 40 years: a study of cystic fibrosis transmembrane conductance regulator function

Published:2010-09-16 Issue:5 Volume:37 Page:1076-1082
ISSN:0903-1936
Container-title:European Respiratory Journal
language:en
Short-container-title:European Respiratory Journal

Author:

Simmonds N. J.,D'Souza L.,Roughton M.,Alton E. W. F. W.,Davies J. C.,Hodson M. E.

Publisher

European Respiratory Society (ERS)

Subject

Pulmonary and Respiratory Medicine

Cited by 28 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. Lung fibrosis: Post-COVID-19 complications and evidences;International Immunopharmacology;2023-03

2. Analysis of CF patient survival confirms STAT3 as a CF-modifying gene with changing impact over time;Human Molecular Genetics;2022-09-01

3. Insights into the variability of nasal potential difference, a biomarker of CFTR activity;Journal of Cystic Fibrosis;2020-07

4. Chloride Conductance, Nasal Potential Difference and Cystic Fibrosis Pathophysiology;Lung;2019-11-16

5. Diagnosis and Presentation of Cystic Fibrosis;Kendig's Disorders of the Respiratory Tract in Children;2019

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