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Molecular Genetics & Genomic Medicine|March 13, 2021
Ex vivo model predicted in vivo efficacy of CFTR modulator therapy in a child with rare genotypeVito Terlizzi, Felice Amato, Chiara Castellani, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|February 16, 2018
Chronic infection sustained by a Pseudomonas aeruginosa High-Risk clone producing the VIM-1 metallo-β-lactamase in a cystic fibrosis patient after lung transplantationSimona Pollini, Claudia Mugnaioli, Daniela Dolce, et al.
Journal of Personalized Medicine|September 23, 2022
Modulator Therapy in Cystic Fibrosis Patients with cis Variants in F508del Complex Allele: A Short-Term Observational Case SeriesVito Terlizzi, Claudia Centrone, Beatrice Ferrari, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|July 25, 2006
Exopolysaccharides produced by clinical strains belonging to the Burkholderia cepacia complexYury Herasimenka, Paola Cescutti, Giuseppe Impallomeni, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|December 16, 2025
Pregnancies in women with cystic fibrosis in the era of CFTR modulators: Current challenges and future perspectives. Insights from the Italian cystic fibrosis registryMarco Salvatore, Giuseppe Campagna, Annalisa Amato, et al.
The Journal of Pediatrics|September 27, 2005
Gestational and neonatal characteristics of children with cystic fibrosis: a cohort studyFilippo Festini, Giovanni Taccetti, Teresa Repetto, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|June 26, 2025
Monitoring early antibiotic treatment with anti-Pseudomonas aeruginosa serology: a comparison of two specific antibody panelsDaniela Dolce, Silvia Campana, Cristina Fevola, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|October 7, 2004
Molecular epidemiology of Pseudomonas aeruginosa, Burkholderia cepacia complex and methicillin-resistant Staphylococcus aureus in a cystic fibrosis centerSilvia Campana, Giovanni Taccetti, Novella Ravenni, et al.
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