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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
Nicole A Taylor,Sheila Sivam,Josie van Dorst et al. Nicole A Taylor et al.
Background: People with cystic fibrosis (pwCF) have increased colorectal cancer (CRC) risk. Colonoscopy is recommended, yet CF comorbidities increase complexity and risk. ...
Stephen E Congly,Ranjani Somayaji,Michael D Parkins et al. Stephen E Congly et al.
The introduction of elexacaftor/tezacaftor/ivacaftor (ETI) has led to improved outcomes and survival in patients living with cystic fibrosis (PwCF) although imposes a substantial economic burden. Despite the reduced healthcare utilization t...
Samantha A Whiteside,John E McGinniss,Rebecca A Deek et al. Samantha A Whiteside et al.
Background: Lung transplantation is commonly required for advanced lung disease in cystic fibrosis (CF). Long-term lung allograft survival is limited primarily by chronic lung allograft dysfunction (CLAD), and microbial f...
Traci M Kazmerski,Olivia M Stransky,Catherine E Wright et al. Traci M Kazmerski et al.
Background: Males with cystic fibrosis (MwCF) face many sexual health concerns that have been understudied. We compared sexual health experiences and care utilization of MwCF to the general population and defined CF-relat...
Amit Saha,Michael Stormon,Peter Lewindon et al. Amit Saha et al.
Background: Cystic fibrosis-related liver disease(CFLD) has long been thought to be secondary to CFTR dysfunction in the biliary epithelial cells causing hepatobiliary complications,eventually progressing to cirrhosis. Ho...
Kari Thrasher,Jianguo Chen,Lianwu Fu et al. Kari Thrasher et al.
Background: Cystic fibrosis patients who carry a CFTR nonsense allele often express negligible CFTR protein, and thus, are unresponsive to CFTR modulators. Nonsense suppression (also called readthrough) is an emerging the...
Laura Schembri,Delyth Jones,Siân Bentley et al. Laura Schembri et al.
Background: Clinical trials showed improved faecal elastase (FE-1) levels in younger children with cystic fibrosis (cwCF) on elexacaftor/tezacaftor/ivacaftor (ETI). Lower sweat chloride has been linked to better clinical ...
Madeline Sanders,Eunjin Hong,Peter S Chung et al. Madeline Sanders et al.
Background: Rifampin is a guideline-recommended treatment for nontuberculous mycobacteria infections; however, it is a strong inducer of CYP3A metabolism and therefore is contraindicated in patients receiving elexacaftor/...