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Elexacaftor/tezacaftor/ivacaftor in children aged 6–11 years with cystic fibrosis, at least one F508DEL allele, and advanced lung disease: A 24‐week observational study.
- Published in:
- Pediatric Pulmonology, 2022, v. 57, n. 9, p. 2253, doi. 10.1002/ppul.25980
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- Article
Effectivenesss of ivacaftor in severe cystic fibrosis patients and non‐G551D gating mutations.
- Published in:
- Pediatric Pulmonology, 2019, v. 54, n. 9, p. 1398, doi. 10.1002/ppul.24424
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- Article
Treatment of Cystic Fibrosis Patients Homozygous for F508del with Lumacaftor-Ivacaftor (Orkambi®) Restores Defective CFTR Channel Function in Circulating Mononuclear Cells.
- Published in:
- International Journal of Molecular Sciences, 2020, v. 21, n. 7, p. 2398, doi. 10.3390/ijms21072398
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- Article
Cystic fibrosis and CFTR-related disorder with electrolyte imbalance at diagnosis: clinical features and outcome in an Italian cohort.
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- European Journal of Pediatrics, 2023, v. 182, n. 12, p. 5275, doi. 10.1007/s00431-023-05193-9
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- Article
CFTR-dependent chloride efflux in cystic fibrosis mononuclear cells is increased by ivacaftor therapy.
- Published in:
- Pediatric Pulmonology, 2017, v. 52, n. 7, p. 900, doi. 10.1002/ppul.23712
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- Article
Clinical course and risk factors for severe COVID-19 among Italian patients with cystic fibrosis: a study within the Italian Cystic Fibrosis Society.
- Published in:
- Infection, 2022, v. 50, n. 3, p. 671, doi. 10.1007/s15010-021-01737-z
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- Article
SARS-CoV-2 infection in cystic fibrosis: A multicentre prospective study with a control group, Italy, February-July 2020.
- Published in:
- PLoS ONE, 2021, v. 16, n. 5, p. 1, doi. 10.1371/journal.pone.0251527
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- Article
G-CSF and GM-CSF Modify Neutrophil Functions at Concentrations found in Cystic Fibrosis.
- Published in:
- Scientific Reports, 2019, v. 9, n. 1, p. N.PAG, doi. 10.1038/s41598-019-49419-z
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- Article