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Published in 2024 at "Pediatric Pulmonology"
DOI: 10.1002/ppul.27123
Abstract: The aerodigestive organs share a kindred embryologic origin that allows for a more complete explanation as to how the foregut can remain a barrier to normalcy in people with cystic fibrosis (pwCF). The structures of…
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Keywords:
disease;
cystic fibrosis;
management;
pwcf ... See more keywords
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3
Published in 2022 at "Journal of Cystic Fibrosis"
DOI: 10.1016/j.jcf.2022.02.012
Abstract: Background : People with cystic fibrosis (pwCF) may be at risk of complications from COVID-19 but the impact of COVID-19 on pwCF remains unknown. Methods : We conducted a multicenter retrospective cohort study to assess…
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Keywords:
impact covid;
cystic fibrosis;
pandemic first;
covid ... See more keywords
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Published in 2021 at "Jornal de pediatria"
DOI: 10.1016/j.jped.2021.05.010
Abstract: OBJECTIVES Cystic fibrosis (CF) is a severe autosomal recessive disease that results from mutations in a gene encoding the Cystic Fibrosis Transmembrane Conductance Regulator (CFTR) protein, a chloride channel. This study aims to characterize the…
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Keywords:
cystic fibrosis;
fibrosis;
pwcf;
candidates new ... See more keywords
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Published in 2021 at "Journal of Cystic Fibrosis"
DOI: 10.1016/s1569-1993(21)01220-0
Abstract: During COVID-19, musculoskeletal (MSK) physiotherapists were redeployed to supplement acute staffing. Virtual clinics (VC) were used by the cystic fibrosis (CF) MDT to assess and monitor patients. Objectives: To scope benefits of providing MSK physiotherapy…
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Keywords:
msk;
pwcf;
cystic fibrosis;
physiotherapy ... See more keywords
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Published in 2025 at "Journal of Proteome Research"
DOI: 10.1021/acs.jproteome.5c00260
Abstract: Fungal infections caused by Scedosporium/Lomentospora species are a significant threat to patients with cystic fibrosis (pwCF), ranking as the second most common filamentous fungi in their airways after Aspergillus. Current serodiagnostic methods, such as counterimmunoelectrophoresis…
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Keywords:
scedosporium;
boydii antigens;
cystic fibrosis;
scedosporium boydii ... See more keywords
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Published in 2024 at "European Heart Journal"
DOI: 10.1093/eurheartj/ehae666.3034
Abstract: Cystic fibrosis (CF) is an autosomal recessive disease affecting multiple organs, however the extent of cardiac involvement in CF is yet to be determined. The remarkable therapeutic advancements with new highly effective CF transmembrane conductance…
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Keywords:
structure function;
function;
sex;
cardiac structure ... See more keywords
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Published in 2024 at "European Heart Journal"
DOI: 10.1093/eurheartj/ehae666.3035
Abstract: Cystic fibrosis (CF) is an autosomal recessive disease affecting multiple organs. Emerging evidence indicates an elevated risk of cardiovascular complications in people with CF (pwCF), with some studies implicating CF-related cardiomyopathy as an underlying mechanism.…
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Keywords:
pain;
dyspnea chest;
cardiac impairment;
pwcf ... See more keywords
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1
Published in 2022 at "mSystems"
DOI: 10.1128/msystems.00364-22
Abstract: The airway microbiome in persons with cystic fibrosis (pwCF) is correlated with lung function and disease severity. Supplemental oxygen use is common in more advanced CF, yet its role in perturbing airway microbial communities is…
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Keywords:
supplemental oxygen;
oxygen;
pwcf;
airway microbiome ... See more keywords
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Published in 2025 at "Microbiology Spectrum"
DOI: 10.1128/spectrum.00382-25
Abstract: ABSTRACT Nontuberculous mycobacterial (NTM) infections in people with cystic fibrosis (pwCF) can have detrimental effects on prognosis and pose significant challenges to treatment. However, there are still questions regarding the contribution and influence of NTMs…
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Keywords:
cftr modulator;
culture;
cystic fibrosis;
pwcf ... See more keywords
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Published in 2022 at "Thorax"
DOI: 10.1136/thorax-2022-219429
Abstract: Cystic fibrosis (CF) is the most common lifelimiting genetic disease. The treatment landscape of CF lung disease is changing dramatically with widespread availability of CF transmembrane conductance regulator (CFTR) modulator treatments targeting the primary protein…
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Keywords:
physical activity;
trial;
activity;
pwcf ... See more keywords
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Published in 2022 at "American Journal of Respiratory Cell and Molecular Biology"
DOI: 10.1165/rcmb.2021-0341le
Abstract: Mutations in CFTR (cystic fibrosis transmembrane regulator) lead indirectly to impaired innate defense of the respiratory tract, and people with cystic fibrosis (PwCF) develop a host of bacterial and fungal infections. The role of viruses…
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Keywords:
genes upregulated;
expression;
f508del;
cluster ... See more keywords