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Profiling the response to lumacaftor‐ivacaftor in children with cystic between fibrosis and new insight from a French‐Italian real‐life cohort.
- Published in:
- Pediatric Pulmonology, 2022, v. 57, n. 12, p. 2992, doi. 10.1002/ppul.26123
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- Publication type:
- Article
Psychological interventions during COVID pandemic: Telehealth for individuals with cystic fibrosis and caregivers.
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- Pediatric Pulmonology, 2021, v. 56, n. 7, p. 1976, doi. 10.1002/ppul.25413
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- Publication type:
- 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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- Publication type:
- Article
Distribution of OGTT-Related Variables in Patients with Cystic Fibrosis from Puberty to Adulthood: An Italian Multicenter Study.
- Published in:
- Journal of Personalized Medicine, 2023, v. 13, n. 3, p. 469, doi. 10.3390/jpm13030469
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- Publication type:
- Article
Theratyping of the Rare CFTR Variants E193K and R334W in Rectal Organoid-Derived Epithelial Monolayers.
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- Journal of Personalized Medicine, 2022, v. 12, n. 4, p. 632, doi. 10.3390/jpm12040632
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- Publication type:
- Article
A Different Microbiome Gene Repertoire in the Airways of Cystic Fibrosis Patients with Severe Lung Disease.
- Published in:
- International Journal of Molecular Sciences, 2017, v. 18, n. 8, p. 1654, doi. 10.3390/ijms18081654
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- Publication type:
- Article
Caregiver burden and vocational participation among parents of adolescents with CF.
- Published in:
- Pediatric Pulmonology, 2016, v. 51, n. 3, p. 243, doi. 10.1002/ppul.23352
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- Publication type:
- Article
Glucose tolerance affects pubertal growth and final height of children with cystic fibrosis.
- Published in:
- Pediatric Pulmonology, 2015, v. 50, n. 2, p. 144, doi. 10.1002/ppul.23042
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- Publication type:
- Article
Usefulness of a program of hospital‐supervised physical training in patients with cystic fibrosis.
- Published in:
- Pediatric Pulmonology, 2004, v. 38, n. 2, p. 115, doi. 10.1002/ppul.20073
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- Publication type:
- Article
Fungal infections of the lung in children.
- Published in:
- 2016
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- Publication type:
- journal article
Liposomes loaded with bioactive lipids enhance antibacterial innate immunity irrespective of drug resistance.
- Published in:
- Scientific Reports, 2017, p. 45120, doi. 10.1038/srep45120
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- Publication type:
- Article
Changes in Cystic Fibrosis Airway Microbial Community Associated with a Severe Decline in Lung Function.
- Published in:
- PLoS ONE, 2015, v. 10, n. 4, p. 1, doi. 10.1371/journal.pone.0124348
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- Publication type:
- Article
Genetic Polymorphisms Affecting IDO1 or IDO2 Activity Differently Associate With Aspergillosis in Humans.
- Published in:
- Frontiers in Immunology, 2019, p. N.PAG, doi. 10.3389/fimmu.2019.00890
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- Publication type:
- Article
An inflammatory Signature of Glucose Impairment in Cystic Fibrosis.
- Published in:
- Journal of Inflammation Research, 2022, v. 15, p. 5677, doi. 10.2147/JIR.S365772
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- Publication type:
- Article
Oral cysteamine as an adjunct treatment in cystic fibrosis pulmonary exacerbations: An exploratory randomized clinical trial.
- Published in:
- PLoS ONE, 2020, v. 15, n. 12, p. 1, doi. 10.1371/journal.pone.0242945
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- Publication type:
- Article
Aryl Hydrocarbon Receptor Agonism Antagonizes the Hypoxia-driven Inflammation in Cystic Fibrosis.
- Published in:
- American Journal of Respiratory Cell & Molecular Biology, 2023, v. 68, n. 3, p. 288, doi. 10.1165/rcmb.2022-0196OC
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- Publication type:
- Article
Untargeted Metagenomic Investigation of the Airway Microbiome of Cystic Fibrosis Patients with Moderate-Severe Lung Disease.
- Published in:
- Microorganisms, 2020, v. 8, n. 7, p. 1003, doi. 10.3390/microorganisms8071003
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- Publication type:
- Article
Liposomes Loaded With Phosphatidylinositol 5-Phosphate Improve the Antimicrobial Response to Pseudomonas aeruginosa in Impaired Macrophages From Cystic Fibrosis Patients and Limit Airway Inflammatory Response.
- Published in:
- Frontiers in Immunology, 2020, v. 11, p. N.PAG, doi. 10.3389/fimmu.2020.532225
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- Publication type:
- Article
A mast cell-ILC2-Th9 pathway promotes lung inflammation in cystic fibrosis.
- Published in:
- Nature Communications, 2017, v. 8, n. 1, p. 14017, doi. 10.1038/ncomms14017
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- Publication type:
- Article
IL-1 receptor antagonist ameliorates inflammasome-dependent inflammation in murine and human cystic fibrosis.
- Published in:
- Nature Communications, 2016, v. 7, n. 3, p. 10791, doi. 10.1038/ncomms10791
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- Publication type:
- Article
HEALTH TECHNOLOGY ASSESSMENT COMO INSTRUMENTO DE EVALUACIÓN ÉTICA EN EL CASO DE LOS TEST GENÉTICOS DE PORTADORES DE FIBROSIS QUÍSTICA.
- Published in:
- Cuadernos de Bioética, 2017, v. 28, n. 3, p. 412
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- Publication type:
- Article
Nuclear Magnetic Resonance-based Metabolomics Discriminates Primary Ciliary Dyskinesia from Cystic Fibrosis.
- Published in:
- 2014
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- Publication type:
- Journal Article
Nuclear Magnetic Resonance-based Metabolomics Discriminates Primary Ciliary Dyskinesia from Cystic Fibrosis.
- Published in:
- American Journal of Respiratory & Critical Care Medicine, 2014, v. 190, n. 2, p. 229, doi. 10.1164/rccm.201402-0249le
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- Publication type:
- Article
Hypoxia Promotes Danger-mediated Inflammation via Receptor for Advanced Glycation End Products in Cystic Fibrosis.
- Published in:
- American Journal of Respiratory & Critical Care Medicine, 2013, v. 188, n. 11, p. 1338, doi. 10.1164/rccm.201305-0986OC
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- Publication type:
- Article
Clinical expression of cystic fibrosis in a large cohort of Italian siblings.
- Published in:
- 2018
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- Publication type:
- journal article
Metabolomic Analysis by Nuclear Magnetic Resonance Spectroscopy as a New Approach to Understanding Inflammation and Monitoring of Pharmacological Therapy in Children and Young Adults With Cystic Fibrosis.
- Published in:
- Frontiers in Pharmacology, 2018, p. N.PAG, doi. 10.3389/fphar.2018.00595
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- Publication type:
- Article
Correction: Pyrosequencing Unveils Cystic Fibrosis Lung Microbiome Differences Associated with a Severe Lung Function Decline.
- Published in:
- 2016
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- Publication type:
- Correction Notice
Pyrosequencing Unveils Cystic Fibrosis Lung Microbiome Differences Associated with a Severe Lung Function Decline.
- Published in:
- PLoS ONE, 2016, v. 11, n. 6, p. 1, doi. 10.1371/journal.pone.0156807
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- Publication type:
- Article
Trans-heterozygosity for mutations enhances the risk of recurrent/chronic pancreatitis in patients with Cystic Fibrosis.
- Published in:
- Molecular Medicine, 2018, v. 24, n. 1, p. N.PAG, doi. 10.1186/s10020-018-0041-6
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- Publication type:
- Article
Extensive Molecular Analysis Suggested the Strong Genetic Heterogeneity of Idiopathic Chronic Pancreatitis.
- Published in:
- Molecular Medicine, 2016, v. 22, n. 1, p. 300, doi. 10.2119/molmed.2016.00010
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- Publication type:
- Article
Extensive Molecular Analysis Suggested the Strong Genetic Heterogeneity of Idiopathic Chronic Pancreatitis.
- Published in:
- Molecular Medicine, 2016, v. 22, p. 300, doi. 10.2119/molmed.2016.00010
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- Publication type:
- Article
Impact of COVID-19 on Lung Disease in People with Cystic Fibrosis: A 6-Month Follow-Up Study on Respiratory Outcomes.
- Published in:
- Biomedicines, 2022, v. 10, n. 11, p. 2771, doi. 10.3390/biomedicines10112771
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- Publication type:
- Article
Slow-release insulin in cystic fibrosis patients with glucose intolerance: a randomized clinical trial.
- Published in:
- Pediatric Diabetes, 2012, v. 13, n. 2, p. 197, doi. 10.1111/j.1399-5448.2011.00810.x
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- Publication type:
- Article
Ionocytes and CFTR Chloride Channel Expression in Normal and Cystic Fibrosis Nasal and Bronchial Epithelial Cells.
- Published in:
- Cells (2073-4409), 2020, v. 9, n. 9, p. 2090, doi. 10.3390/cells9092090
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- Publication type:
- Article
New PRSS1 and common CFTR mutations in a child with acute recurrent pancreatitis, could be considered an "Hereditary" form of pancreatitis ?
- Published in:
- 2010
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- Publication type:
- journal article
New PRSS1 and common CFTR mutations in a child with acute recurrent pancreatitis, could be considered an "Hereditary" form of pancreatitis?
- Published in:
- BMC Gastroenterology, 2010, v. 10, p. 119, doi. 10.1186/1471-230X-10-119
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- Publication type:
- Article
Segregation analysis in cystic fibrosis at-risk family demonstrates that the M348K CFTR mutation is a rare innocuous polymorphism.
- Published in:
- Prenatal Diagnosis, 2004, v. 24, n. 12, p. 981, doi. 10.1002/pd.1058
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- Publication type:
- Article
Methicillin-resistant Staphylococcus aureus eradication in cystic fibrosis patients: A randomized multicenter study.
- Published in:
- PLoS ONE, 2019, v. 14, n. 3, p. 1, doi. 10.1371/journal.pone.0213497
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- Publication type:
- Article
Gut microbiota signatures in cystic fibrosis: Loss of host CFTR function drives the microbiota enterophenotype.
- Published in:
- PLoS ONE, 2018, v. 13, n. 12, p. 1, doi. 10.1371/journal.pone.0208171
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- Publication type:
- Article
Clinical hallmarks and genetic polymorphisms in the CFTR gene contribute to the disclosure of the A1006E mutation.
- Published in:
- Clinical & Investigative Medicine, 2010, v. 33, n. 4, p. E234, doi. 10.25011/cim.v33i4.14226
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- Publication type:
- Article
Severity of SARS-CoV-2 infection in a hospital population: a clinical comparison across age groups.
- Published in:
- Italian Journal of Pediatrics, 2023, v. 49, n. 1, p. 1, doi. 10.1186/s13052-023-01485-w
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- Publication type:
- Article
A Metagenomic and in Silico Functional Prediction of Gut Microbiota Profiles May Concur in Discovering New Cystic Fibrosis Patient-Targeted Probiotics.
- Published in:
- Nutrients, 2017, v. 9, n. 12, p. 1342, doi. 10.3390/nu9121342
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- Publication type:
- Article
Coping with cystic fibrosis: An analysis from the sibling's point of view.
- Published in:
- Child: Care, Health & Development, 2021, v. 47, n. 6, p. 825, doi. 10.1111/cch.12890
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- Publication type:
- Article
Molecular analysis using DHPLC of cystic fibrosis: increase of the mutation detection rate among the affected population in Central Italy.
- Published in:
- BMC Medical Genetics, 2004, v. 5, p. 8, doi. 10.1186/1471-2350-5-8
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- Publication type:
- Article