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Publications by Maria C Maiuri
Cysteamine Re-Establishes the Clearance of Pseudomonas Aeruginosa by Macrophages Bearing the Cystic Fibrosis-Relevant F508del-CFTR Mutation
Cell Death and Disease
Molecular Neuroscience
Immunology
Cell Biology
Cancer Research
Cellular
Medicine
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The Cystic Fibrosis F508del Mutation in Crohn's Disease
Journal of Cystic Fibrosis
Child Health
Pulmonary
Pediatrics
Perinatology
Respiratory Medicine
Cystic Fibrosis Transmembrane Conductance Regulator (CFTR)-Mediated Residual Chloride Secretion Does Not Protect Against Early Chronic Pseudomonas Aeruginosa Infection in F508del Homozygous Cystic Fibrosis Patients
Pediatric Research
Child Health
Pediatrics
Perinatology
Impaired CFTR Function in Mild Cystic Fibrosis Associated With the S977f/T5TG12complex Allele in Trans With F508del Mutation
Journal of Cystic Fibrosis
Child Health
Pulmonary
Pediatrics
Perinatology
Respiratory Medicine
Eradication of Pseudomonas Aeruginosa in Cystic Fibrosis
European Respiratory Journal
Medicine
Pulmonary
Respiratory Medicine
Dysfunctional CFTR Alters the Bactericidal Activity of Human Macrophages Against Pseudomonas Aeruginosa
PLoS ONE
Multidisciplinary
Thymosin Α-1 Does Not Correct F508del-CFTR in Cystic Fibrosis Airway Epithelia
JCI insight
Medicine
Thymosin Α-1 Does Not Correct F508del-CFTR in Cystic Fibrosis Airway Epithelia
JCI insight
Medicine
Treatment of Pseudomonas Aeruginosa Colonisation in Cystic Fibrosis.
Archives of Disease in Childhood
Child Health
Pediatrics
Perinatology
Phenotypic Expression of the p.Leu1077Pro CFTR Mutation in Sicilian Cystic Fibrosis Patients
BMC Research Notes
Biochemistry
Medicine
Genetics
Molecular Biology
