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Factors increasing the risk for stone formation in adult patients with cystic fibrosis.
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- Nephrology Dialysis Transplantation, 2006, v. 21, n. 7, p. 1870
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- Article
Clinical expression of cystic fibrosis in a large cohort of Italian siblings.
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- 2018
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- Publication type:
- journal article
Cystic Fibrosis: Recent Insights into Inhaled Antibiotic Treatment and Future Perspectives.
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- Antibiotics (2079-6382), 2021, v. 10, n. 3, p. 338, doi. 10.3390/antibiotics10030338
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- Article
Influence of pancreatic status on circulating plasma sterols in patients with cystic fibrosis.
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- Clinical Chemistry & Laboratory Medicine, 2020, v. 58, n. 10, p. 1725, doi. 10.1515/cclm-2019-1112
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- Article
Reduced absorption and enhanced synthesis of cholesterol in patients with cystic fibrosis: a preliminary study of plasma sterols.
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- Clinical Chemistry & Laboratory Medicine, 2016, v. 54, n. 9, p. 1461, doi. 10.1515/cclm-2015-1151
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- Article
Effectivenesss of ivacaftor in severe cystic fibrosis patients and non‐G551D gating mutations.
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- Pediatric Pulmonology, 2019, v. 54, n. 9, p. 1398, doi. 10.1002/ppul.24424
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- Article
Liver biochemical indexes and cholesterol metabolism in cystic fibrosis patients with F508del/CFTR variant genotype after elexacaftor/tezacaftor/ivacaftor treatment.
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- Scientific Reports, 2024, v. 14, n. 1, p. 1, doi. 10.1038/s41598-024-68511-7
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- Article
Lung structure and function similarities between primary ciliary dyskinesia and mild cystic fibrosis: a pilot study.
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- Italian Journal of Pediatrics, 2017, v. 43, p. 1, doi. 10.1186/s13052-017-0351-2
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- Article
Employment Status and Work Ability in Adults with Cystic Fibrosis.
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- International Journal of Environmental Research & Public Health, 2021, v. 18, n. 22, p. 11776, doi. 10.3390/ijerph182211776
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- Article
TAS2R38 is a novel modifier gene in patients with cystic fibrosis.
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- Scientific Reports, 2020, v. 10, n. 1, p. 1, doi. 10.1038/s41598-020-62747-9
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- Article
The Diagnosis of Cystic Fibrosis in Adult Age. Data from the Italian Registry.
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- Diagnostics (2075-4418), 2021, v. 11, n. 2, p. 321, doi. 10.3390/diagnostics11020321
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- Article
Impaired Ratio of Unsaturated to Saturated Non-Esterified Fatty Acids in Saliva from Patients with Cystic Fibrosis.
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- Diagnostics (2075-4418), 2020, v. 10, n. 11, p. 915, doi. 10.3390/diagnostics10110915
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- Article
Salivary Cytokines and Airways Disease Severity in Patients with Cystic Fibrosis.
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- Diagnostics (2075-4418), 2020, v. 10, n. 4, p. 222, doi. 10.3390/diagnostics10040222
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- Publication type:
- Article
Incidental late diagnosis of cystic fibrosis following AH1N1 influenza virus pneumonia: a case report.
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- 2017
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- Publication type:
- journal article
Cystic Fibrosis: The Sense of Smell.
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- American Journal of Rhinology & Allergy, 2020, v. 34, n. 1, p. 35, doi. 10.1177/1945892419870450
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- Article
A New Method to Improve the Clinical Evaluation of Cystic Fibrosis Patients by Mucus Viscoelastic Properties.
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- PLoS ONE, 2014, v. 9, n. 1, p. 1, doi. 10.1371/journal.pone.0082297
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- Article
Use of mucoactive agents in cystic fibrosis: A consensus survey of Italian specialists.
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- Health Science Reports, 2022, v. 5, n. 4, p. 1, doi. 10.1002/hsr2.604
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- Publication type:
- Article
One year of treatment with elexacaftor/tezacaftor/ivacaftor in patients with cystic fibrosis homozygous for the F508del mutation causes a significant increase in liver biochemical indexes.
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- Frontiers in Molecular Biosciences, 2024, p. 01, doi. 10.3389/fmolb.2023.1327958
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- Article
Adiponectin Expression Is Modulated by Long-Term Physical Activity in Adult Patients Affected by Cystic Fibrosis.
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- Mediators of Inflammation, 2019, p. 1, doi. 10.1155/2019/2153934
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- Article
Microbiology of airway disease in a cohort of patients with Cystic Fibrosis.
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- BMC Infectious Diseases, 2006, v. 6, n. 1, p. 4, doi. 10.1186/1471-2334-6-4
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- Article
Clinical outcome of individuals carrying 5T;TG12 in trans with CFTR variants with varying clinical consequences.
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- Pediatric Pulmonology, 2023, v. 58, n. 4, p. 1253, doi. 10.1002/ppul.26323
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- Article
Disease characterization of people with cystic fibrosis and a minimal function mutation: Data from the Italian registry.
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- Pediatric Pulmonology, 2021, v. 56, n. 10, p. 3232, doi. 10.1002/ppul.25616
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- Article
Cystic fibrosis with non‐G551D gating mutations in Italy: Epidemiology and clinical characteristics.
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- Pediatric Pulmonology, 2021, v. 56, n. 2, p. 442, doi. 10.1002/ppul.25179
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- Article
Lipidomic alterations in human saliva from cystic fibrosis patients.
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- Scientific Reports, 2023, v. 13, n. 1, p. 1, doi. 10.1038/s41598-022-24429-6
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- Article
Supervised physical exercise improves clinical, anthropometric and biochemical parameters in adult cystic fibrosis patients: A 2‐year evaluation.
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- Clinical Respiratory Journal, 2018, v. 12, n. 7, p. 2228, doi. 10.1111/crj.12796
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- Article
Physical Activity Regulates TNFα and IL-6 Expression to Counteract Inflammation in Cystic Fibrosis Patients.
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- International Journal of Environmental Research & Public Health, 2021, v. 18, n. 9, p. 4691, doi. 10.3390/ijerph18094691
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- Article
Cystic Fibrosis in Adults: A Paradigm of Frailty Syndrome? An Observational Study.
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- Journal of Clinical Medicine, 2024, v. 13, n. 2, p. 585, doi. 10.3390/jcm13020585
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- Article
Cystic Fibrosis Patients with F508del/Minimal Function Genotype: Laboratory and Nutritional Evaluations after One Year of Elexacaftor/Tezacaftor/Ivacaftor Treatment.
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- Journal of Clinical Medicine, 2022, v. 11, n. 23, p. 6900, doi. 10.3390/jcm11236900
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- Article
Elexacaftor/Tezacaftor/Ivacaftor in Patients with Cystic Fibrosis Homozygous for the F508del Mutation and Advanced Lung Disease: A 48-Week Observational Study.
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- Journal of Clinical Medicine, 2022, v. 11, n. 4, p. N.PAG, doi. 10.3390/jcm11041021
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- Publication type:
- Article
Extensive CFTR Gene Analysis Revealed a Higher Occurrence of Cystic Fibrosis Transmembrane Regulator-Related Disorders (CFTR-RD) among CF Carriers.
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- Journal of Clinical Medicine, 2020, v. 9, n. 12, p. 3853, doi. 10.3390/jcm9123853
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- Article
Oxylipin profile in saliva from patients with cystic fibrosis reveals a balance between pro-resolving and pro-inflammatory molecules.
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- Scientific Reports, 2022, v. 12, n. 1, p. 1, doi. 10.1038/s41598-022-09618-7
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- Publication type:
- Article
Totally implantable central venous access ports in patients with cystic fibrosis: a multicenter prospective cohort study.
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- Journal of Vascular Access, 2012, v. 13, n. 3, p. 290, doi. 10.5301/jva.5000036
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- Article