156 results on '"Anagnostopoulou, Pinelopi"'
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2. Demographic characteristics, clinical and laboratory features, and the distribution of pathogenic variants in the CFTR gene in the Cypriot cystic fibrosis (CF) population demonstrate the utility of a national CF patient registry
3. Anatomy and development of the respiratory system
4. Variability of Tidal Breathing Parameters in Preterm Infants and Associations with Respiratory Morbidity during Infancy: A Cohort Study
5. Respiratory rate in infants with cystic fibrosis throughout the first year of life and association with lung clearance index measured shortly after birth
6. A BEAT-PCD consensus statement: a core outcome set for pulmonary disease interventions in primary ciliary dyskinesia
7. Airspace Diameter Map—A Quantitative Measurement of All Pulmonary Airspaces to Characterize Structural Lung Diseases
8. Possible founder effect and prevalence of the p.Cys1400Ter pathogenic CFTR mutation in Cyprus
9. Lung clearance index as a marker of lung functional impairment in primary ciliary dyskinesia: preliminary results of a systematic review of the literature
10. Impact of exposure reduction recommendations on health outcomes in children with asthma during high desert dust season in Greece and Cyprus: Results of the MEDEA randomised trial
11. In neonatal βENaC-transgenic mice CF-like lung disease causes a dilatation of the conducting airways which increases until adulthood
12. A BEAT-PCD consensus statement: a core outcome set for pulmonary disease interventions in primary ciliary dyskinesia.
13. Improved childhood asthma control after exposure reduction interventions for desert dust and anthropogenic air pollution: the MEDEA randomised controlled trial
14. MEDEA randomised intervention study protocol in Cyprus, Greece and Israel for mitigation of desert dust health effects in adults with atrial fibrillation
15. Observational study of health utilities in adult primary ciliary dyskinesia patients: preliminary data on associations with molecular diagnosis, clinical phenotype and HRQOL measures
16. A modified CO2/O2 Guedel airway improves capnographic accuracy compared with a CO2/O2 nasal cannula: An infant manikin study
17. The disease-specific clinical trial network for primary ciliary dyskinesia:PCD-CTN
18. Interrupter technique in infancy: Higher airway resistance and lower short‐term variability in preterm versus term infants
19. Normative multiple-breath washout data in school-aged children corrected for sensor error
20. The disease-specific clinical trial network for primary ciliary dyskinesia: PCD-CTN
21. Increased Impact of Air Pollution on Lung Function in Preterm versus Term Infants: The BILD Study
22. Pediatric asthma symptom control during lockdown for the COVID‐19 pandemic in Spring 2020: A prospective community‐based study in Cyprus and Greece
23. False normal Lung Clearance Index in infants with cystic fibrosis due to software algorithms
24. Compliance of asthmatic children to lockdown measures for the COVID-19 pandemic: Objective assessment using wearable sensors
25. Neonatal ßENaC-Tg mice with cystic fibrosis-like lung disease possess enlarged airspaces
26. Prospective assessment of pediatric asthma morbidity in Cyprus and Greece during COVID-19 lockdown measures in Spring 2020
27. Additional file 1 of Demographic characteristics, clinical and laboratory features, and the distribution of pathogenic variants in the CFTR gene in the Cypriot cystic fibrosis (CF) population demonstrate the utility of a national CF patient registry
28. SLC26A9-mediated chloride secretion prevents mucus obstruction in airway inflammation
29. A multi-scale model of gas transport in the lung to study heterogeneous lung ventilation during the multiple-breath washout test
30. An innovative lung model for multiple breath washout testing in health and disease
31. Efficacy and safety of the combination fluticasone propionate plus salmeterol in asthmatic preschoolers: An observational study
32. Demographic Characteristics, Clinical and Laboratory Features, and The Distribution of Pathogenic Variants In the Cftr Gene In the Cypriot Cystic Fibrosis (Cf) Population Demonstrate The Utility of a National Cf Patient Registry
33. Normative data for multiple breath washout outcomes in school-aged Caucasian children
34. Implementation of multigene panel NGS diagnosis in the national primary ciliary dyskinesia cohort of Cyprus: An island with a high disease prevalence
35. mCLCA3 Does Not Contribute to Calcium-Activated Chloride Conductance in Murine Airways
36. Dehydration and electrolyte imbalance: a common presenting manifestation of cystic fibrosis in Cyprus
37. Health state utilities in adult Primary Ciliary Dyskinesia patients
38. Use of wearable sensors to assess compliance of asthmatic children in response to lockdown measures for the COVID-19 epidemic
39. Evaluation of a multiple breath nitrogen washout system in children
40. Comparison of different analysis algorithms to calculate multiple-breath washout outcomes
41. Infant multiple breath washout using a new commercially available device: Ready to replace the previous setup?
42. Pediatric asthma symptom control during lockdown for the COVID‐19 pandemic in Spring 2020: A prospective community‐based study in Cyprus and Greece.
43. Observational study of health utilities in adult primary ciliary dyskinesia patients: preliminary data on associations with molecular diagnosis, clinical phenotype and HR-QoL measures.
44. Lower exhaled nitric oxide in infants with Cystic Fibrosis compared to healthy controls
45. Infant multiple breath washout using a new commercially available device: Ready to replace the previous setup?
46. Normative data for multiple breath washout outcomes in school-aged Caucasian children
47. A mathematical model to understand the airway clearance in cystic fibrosis
48. A multi-scale model of gas transport in the lung to study heterogeneous lung ventilation during the multiple-breath washout test
49. An innovative lung model for multiple breath washout testing in health and disease
50. Variability of Tidal Breathing Parameters in Preterm Infants and Associations with Respiratory Morbidity during Infancy: A Cohort Study
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