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Orphanet Journal of Rare Diseases|March 6, 2019
Is early detection of late-onset Pompe disease a pneumologist's affair? A lesson from an Italian screening studyMarco Confalonieri, Michele Vitacca, Raffaele Scala, et al.
Medicina (Kaunas, Lithuania)|August 26, 2022
Chronic Thromboembolic Pulmonary Hypertension: An Observational StudyBarbara Ruaro, Paola Confalonieri, Gaetano Caforio, et al.
Diagnostics (Basel, Switzerland)|April 30, 2021
Evaluation of Correlations between Genetic Variants and High-Resolution Computed Tomography Patterns in Idiopathic Pulmonary FibrosisElisa Baratella, Barbara Ruaro, Fabiola Giudici, et al.
Pharmaceuticals (Basel, Switzerland)|January 23, 2024
Functional Progression after Dose Suspension or Discontinuation of Nintedanib in Idiopathic Pulmonary Fibrosis: A Real-Life Multicentre StudyBarbara Ruaro, Andrea Salotti, Nicolò Reccardini, et al.
Respiratory Medicine|January 2, 2026
Sex Differences in Low Arousal Threshold in Obstructive Sleep ApneaGloria Maria Citton, Caterina Antonaglia, Antonio Fabozzi, et al.
Diagnostics (Basel, Switzerland)|February 25, 2022
Chronic Thromboembolic Pulmonary Hypertension: An UpdateBarbara Ruaro, Elisa Baratella, Gaetano Caforio, et al.
Heart & Lung : the Journal of Critical Care|July 20, 2025
Indirect evaluation of lung condition by means of LF-NMR following chest physiotherapy or ETI administration in cystic-fibrosis patientsMichela Abrami, Alice Biasin, Massimo Maschio, et al.
Drug Delivery and Translational Research|March 14, 2022
Effect of chest physiotherapy on cystic fibrosis sputum nanostructure: an experimental and theoretical approachMichela Abrami, Massimo Maschio, Massimo Conese, et al.
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