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期刊名:Journal of cystic fibrosis

缩写:J CYST FIBROS

ISSN:1569-1993

e-ISSN:1873-5010

IF/分区:6.0/Q1

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共收录本刊相关文章索引2548
Clinical Trial Case Reports Meta-Analysis RCT Review Systematic Review
Classical Article Case Reports Clinical Study Clinical Trial Clinical Trial Protocol Comment Comparative Study Editorial Guideline Letter Meta-Analysis Multicenter Study Observational Study Randomized Controlled Trial Review Systematic Review
C Smith,H K Chadwick,N Shaw et al. C Smith et al.
Background: Clarity and consistency of required knowledge and skills is crucial in supporting the development of members of cystic fibrosis (CF) multidisciplinary teams. Syllabi are effective frameworks for delivering a m...
Yuxin Chen,Daan Caudri,Eleni-Rosalina Andrinopoulou et al. Yuxin Chen et al.
Background: Cystic fibrosis (CF) lung disease begins early in life and progresses throughout childhood into adolescence. Children completing the Australasian CF Bronchoalveolar Lavage (ACFBAL) trial were followed longitud...
Elsie Clarke,Joshua Gardner,Alanood Howsawi et al. Elsie Clarke et al.
Background: The introduction of CFTR modulators has been transformative for many people with cystic fibrosis (CF). The drugs are generally well tolerated although adverse reactions such as delayed-type T-cell mediated hyp...
Nazanin Abolhassani,Kim Dao,Roberta Noseda et al. Nazanin Abolhassani et al.
Background: Cystic fibrosis transmembrane conductance regulator (CFTR) modulators have transformed the management of cystic fibrosis (CF), but evidence on their safety during pregnancy remains limited and pregnancy-relate...
Solène Castanier,Ahmad Elbahnsi,Benoit Chevalier et al. Solène Castanier et al.
The Cystic Fibrosis Transmembrane conductance Regulator (CFTR) modulator VX-445 (Elexacaftor) used to treat cystic fibrosis presents both corrector and potentiator activities. This drug binds to a pocket within the CFTR membrane-spanning do...
Laure Alexandre-Heymann,Quitterie Reynaud,Caroline Grou et al. Laure Alexandre-Heymann et al.
Background: Systematic screening for cystic fibrosis related diabetes (CFRD) is recommended for all people living with cystic fibrosis (pwCF) from the age of 10. However, adhering to these guidelines is challenging given ...
Valeria Rimoldi,Giulia Soldà,Anita Capalbo et al. Valeria Rimoldi et al.
Background: Cystic Fibrosis (CF) results from CFTR gene mutations, including splicing defects such as the polymorphic TGnTm repeat, which disrupts exon-10 inclusion and contributes to CF monosymptomatic forms. While recen...
Fabiana Ciciriello,Andrea Foppiani,Federica Sileo et al. Fabiana Ciciriello et al.
Background: People with Cystic Fibrosis (pwCF) often exhibit impaired insulin secretion, which may lead to Cystic Fibrosis-Related Diabetes (CFRD). The impact of CF variants in the complex relationship between CFTR channe...
Angelica Squarzoni,Gaia Boschetti,Sine Mandrup Bertozzi et al. Angelica Squarzoni et al.
Background: We previously demonstrated that Tezacaftor inhibits the enzyme (DEGS) that converts dihydroceramides (dHCer) into ceramides, thus producing accumulation of dHCer in various cells and tissues. We here conducted...