Dornase alfa in Cystic Fibrosis: indications, comparative studies and effects on lung clearance index by Vito Terlizzi, Chiara Castellani, Giovanni Taccetti, Beatrice Ferrari

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G378X‐I148T CFTR variant: A new complex allele in a cystic fibrosis newborn with pancreatic insufficiency by Vito Terlizzi, Claudia Centrone, Matteo Botti, Giovanni Taccetti

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Can percussive intrapulmonary ventilation improve the efficacy of physiotherapy in children with cystic fibrosis? by Diletta Innocenti, Chiara Castellani, Eleonora Masi, Valeria Galici, Letizia Macconi, Giovanni Taccetti

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Management of pulmonary aspergillosis in children: a systematic review by Vito Terlizzi, Marco Antonio Motisi, Roberta Pellegrino, Luisa Galli, Giovanni Taccetti, Elena Chiappini

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Concomitant Use of Elexacaftor/Tezacaftor/Ivacaftor and Etanercept in a Cystic Fibrosis Patient with Juvenile Idiopathic Arthritis by Sara Immacolata Orsini, Edoardo Marrani, Ilaria Pagnini, Giovanni Taccetti, Vito Terlizzi, Gabriele Simonini

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Early Effects of Elexacaftor-Tezacaftor-Ivacaftor Therapy on Magnetic Resonance Imaging in Patients with Cystic Fibrosis and Advanced Lung Disease by Letizia Macconi, Valeria Galici, Marco Di Maurizio, Enrica Rossi, Giovanni Taccetti, Vito Terlizzi

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Cystic Fibrosis: Recent Insights into Inhaled Antibiotic Treatment and Future Perspectives by Giovanni Taccetti, Michela Francalanci, Giovanna Pizzamiglio, Barbara Messore, Vincenzo Carnovale, Giuseppe Cimino, Marco Cipolli

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Effect of Dornase Alfa on the Lung Clearance Index in Children with Cystic Fibrosis: A Lesson from a Case Series by Vito Terlizzi, Giuseppe Fabio Parisi, Beatrice Ferrari, Chiara Castellani, Sara Manti, Salvatore Leonardi, Giovanni Taccetti

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Ex vivo model predicted in vivo efficacy of CFTR modulator therapy in a child with rare genotype by Vito Terlizzi, Felice Amato, Chiara Castellani, Beatrice Ferrari, Luis J. V. Galietta, Giuseppe Castaldo, Giovanni Taccetti

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Modulator Therapy in Cystic Fibrosis Patients with <i>cis</i> Variants in F508del Complex Allele: A Short-Term Observational Case Series by Vito Terlizzi, Claudia Centrone, Beatrice Ferrari, Chiara Castellani, Tarini N. A. Gunawardena, Giovanni Taccetti, Onofrio Laselva

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Comparison between Gibson–Cooke and Macroduct Methods in the Cystic Fibrosis Neonatal Screening Program and in Subjects Who Are Cystic Fibrosis Screen-Positive with an Inconclusive... by Daniela Dolce, Cristina Fevola, Erica Camera, Tommaso Orioli, Ersilia Lucenteforte, Marco Andrea Malanima, Giovanni Taccetti, Vito Terlizzi

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Extensive <i>CFTR</i> Gene Analysis Revealed a Higher Occurrence of Cystic Fibrosis Transmembrane Regulator-Related Disorders (CFTR-RD) among CF Carriers by Maria Valeria Esposito, Achille Aveta, Marika Comegna, Gustavo Cernera, Paola Iacotucci, Vincenzo Carnovale, Giovanni Taccetti, Vito Terlizzi, Giuseppe Castaldo

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Elexacaftor–Tezacaftor–Ivacaftor Therapy for Cystic Fibrosis Patients with The F508del/Unknown Genotype by Marika Comegna, Vito Terlizzi, Donatello Salvatore, Carmela Colangelo, Antonella Miriam Di Lullo, Immacolata Zollo, Giovanni Taccetti, Giuseppe Castaldo, Felice Amato

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A Multicentre Italian Study on the Psychological Impact of an Inconclusive Cystic Fibrosis Diagnosis after Positive Neonatal Screening by Antonella Tosco, Diletta Marino, Sara Polizzi, Valentina Tradati, Rita Padoan, Claudia Giust, Benedetta Fabrizzi, Giovanni Taccetti, Lucia Merli, Vito Terlizzi

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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... by Alice Castaldo, Alice Castaldo, Alice Castaldo, Monica Gelzo, Monica Gelzo, Paola Iacotucci, Annalisa Longobardi, Giovanni Taccetti, Vito Terlizzi, Vincenzo Carnovale

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Clinical and Genotypical Features of False-Negative Patients in 26 Years of Cystic Fibrosis Neonatal Screening in Tuscany, Italy by Giovanni Taccetti, Matteo Botti, Vito Terlizzi, Maria Chiara Cavicchi, Anna Silvia Neri, Valeria Galici, Gianfranco Mergni, Claudia Centrone, Diego G. Peroni, Filippo Festini

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CRMS/CFSPID Subjects Carrying D1152H CFTR Variant: Can the Second Variant Be a Predictor of Disease Development? by Vito Terlizzi, Rita Padoan, Laura Claut, Carla Colombo, Benedetta Fabrizzi, Marco Lucarelli, Sabina Maria Bruno, Alice Castaldo, Paolo Bonomi, Giovanni Taccetti, Antonella Tosco

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Impact of Pancreatitis-Associated Protein on Newborn Screening Outcomes and Detection of CFTR-Related Metabolic Syndrome (CRMS)/Cystic Fibrosis Screen Positive, Inconclusive Diagno... by Chiara Bianchimani, Daniela Dolce, Claudia Centrone, Silvia Campana, Novella Ravenni, Tommaso Orioli, Erica Camera, Gianfranco Mergni, Cristina Fevola, Paolo Bonomi, Giovanni Taccetti, Vito Terlizzi

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Clinical Consequences and Functional Impact of the Rare S737F CFTR Variant and Its Responsiveness to CFTR Modulators by Vito Terlizzi, Emanuela Pesce, Valeria Capurro, Valeria Tomati, Mariateresa Lena, Cristina Pastorino, Renata Bocciardi, Federico Zara, Claudia Centrone, Giovanni Taccetti, Carlo Castellani, Nicoletta Pedemonte

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Cystic fibrosis in Tuscany: evolution of newborn screening strategies over time to the present by Matteo Botti, Vito Terlizzi, Michela Francalanci, Daniela Dolce, Maria Chiara Cavicchi, Anna Silvia Neri, Valeria Galici, Gianfranco Mergni, Lucia Zavataro, Claudia Centrone, Filippo Festini, Giovanni Taccetti

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