Debora Maj
Pisa, Italy
Last Updated: 09/26/2026
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Found 10 publications
Pulmonary exacerbations in patients with genetically confirmed PCD: a prospective observational multicentre study.
Journal: Frontiers in molecular biosciences
Published: December 14, 2025
Enhancing genetic diagnosis of primary ciliary dyskinesia by copy number variants analysis.
Journal: Respiratory medicine
Published: October 10, 2025
Towards a practical tool to identify HYDIN genotype using high-speed videomicroscopy.
Journal: Thorax
Published: October 10, 2025
Effectiveness of a targeted infant RSV immunization strategy (2024-2025): A multicenter matched case-control study in a high-surveillance setting.
Journal: The Journal of infection
Published: May 17, 2025
Is Lung Function Decline Always Severe in Primary Ciliary Dyskinesia Due to Mutations in CCNO Gene?
Journal: Pediatric pulmonology
Published: October 21, 2024
Impact of TAS2R38 polymorphisms on nasal nitric oxide and Pseudomonas infections in primary ciliary dyskinesia: relation to genotype.
Journal: Thorax
Published: January 08, 2024
Analyses of 1236 genotyped primary ciliary dyskinesia individuals identify regional clusters of distinct DNA variants and significant genotype-phenotype correlations.
Journal: The European respiratory journal
Published: October 17, 2023
The genetic framework of primary ciliary dyskinesia assessed by soft computing analysis.
Journal: Pediatric pulmonology
Published: August 25, 2023
Showing 1-10 of 10
Last Updated: 09/26/2026