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Thorax|October 10, 2025
Towards a practical tool to identify HYDIN genotype using high-speed videomicroscopyMassimo Pifferi, Attilio Boner, Debora Maj, et al.
Respiratory Medicine|April 30, 2026
Enhancing Genetic Diagnosis of Primary Ciliary Dyskinesia by Copy Number Variants AnalysisVeronica Bertini, Massimo Pifferi, Teresa Ramone, et al.
Pediatric Pulmonology|January 3, 2024
The genetic framework of primary ciliary dyskinesia assessed by soft computing analysisMassimo Pifferi, Attilio L Boner, Angela Cangiotti, et al.
Chest|July 1, 2022
Longitudinal Nitric Oxide Levels and Infections by Ultrastructure and Genotype in Primary Ciliary DyskinesiaMassimo Pifferi, Attilio L Boner, Serena Gracci, et al.
Thorax|August 24, 2024
Impact of TAS2R38 polymorphisms on nasal nitric oxide and Pseudomonas infections in primary ciliary dyskinesia: relation to genotypeMassimo Pifferi, Attilio Boner, Debora Maj, et al.
Human Gene Therapy|April 29, 2026
AAV-Mediated Base Editing for Correction of RSPH4A Mutations in Primary Ciliary Dyskinesia: A Proof-of-Concept StudyAlessandro De Carli, Sara Pastore, Debora Maj, et al.
The Journal of Infection|August 23, 2025
Effectiveness of a targeted infant RSV immunization strategy (2024-2025): A multicenter matched case-control study in a high-surveillance settingFederica Attaianese, Sandra Trapani, Rino Agostiniani, et al.
Frontiers in Molecular Biosciences|July 10, 2026
Pulmonary exacerbations in patients with genetically confirmed PCD: a prospective observational multicentre studyPinelopi Anagnostopoulou, Panayiotis Kouis, Dilber Ademhan Tural, et al.
The European Respiratory Journal|June 13, 2024
Analyses of 1236 genotyped primary ciliary dyskinesia individuals identify regional clusters of distinct DNA variants and significant genotype-phenotype correlationsJohanna Raidt, Sarah Riepenhausen, Petra Pennekamp, et al.
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