106 results on '"Tiddens, Harm A.W.M."'
Search Results
2. The clinical impact of Lumacaftor-Ivacaftor on structural lung disease and lung function in children aged 6–11 with cystic fibrosis in a real-world setting
3. Automatic bronchus and artery analysis on chest computed tomography to evaluate the effect of inhaled hypertonic saline in children aged 3-6 years with cystic fibrosis in a randomized clinical trial
4. Macrophage PD-1 associates with neutrophilia and reduced bacterial killing in early cystic fibrosis airway disease
5. Association between early respiratory viral infections and structural lung disease in infants with cystic fibrosis
6. The effect of inhaled hypertonic saline on lung structure in children aged 3–6 years with cystic fibrosis (SHIP-CT): a multicentre, randomised, double-blind, controlled trial
7. Bronchiectasis and inhaled tobramycin: A literature review
8. Diaphragmatic dysfunction in neuromuscular disease, an MRI study
9. A clinical guideline for structured assessment of CT-imaging in congenital lung abnormalities
10. quantitative ct imaging analysis to predict Pathology features in patients with a Congenital Pulmonary Airway Malformation
11. Diagnosis and quantification of bronchiectasis using computed tomography or magnetic resonance imaging: A systematic review
12. The impact of chest computed tomography and chest radiography on clinical management of cystic fibrosis lung disease
13. Guidance for computed tomography (CT) imaging of the lungs for patients with cystic fibrosis (CF) in research studies
14. Azithromycin reduces bronchial wall thickening in infants with cystic fibrosis
15. Oxidative stress and abnormal bioactive lipids in early cystic fibrosis lung disease
16. The evolving role of radiological imaging in cystic fibrosis
17. Chest imaging in cystic fibrosis studies: What counts, and can be counted?
18. The fate of inhaled antibiotics after deposition in cystic fibrosis: How to get drug to the bug?
19. Objective airway artery dimensions compared to CT scoring methods assessing structural cystic fibrosis lung disease
20. Daily Observations of Nebuliser Use and Technique (DONUT) in children with cystic fibrosis
21. Reversibility of trapped air on chest computed tomography in cystic fibrosis patients
22. Bronchiectases at early chest computed tomography in children with cystic fibrosis are associated with increased risk of subsequent pulmonary exacerbations and chronic pseudomonas infection
23. Multi-modality monitoring of cystic fibrosis lung disease: The role of chest computed tomography
24. Quantitative assessment of airway dimensions in young children with cystic fibrosis lung disease using chest computed tomography
25. Spirometer guided chest imaging in children: It is worth the effort!
26. A network meta-analysis of the efficacy of inhaled antibiotics for chronic Pseudomonas infections in cystic fibrosis
27. Pulmonary Ventilation and Micro-Structural Findings in Congenital Diaphragmatic Hernia
28. Validating Chest MRI to Detect and Monitor Cystic Fibrosis Lung Disease in a Pediatric Cohort
29. Respiratory Tract Exacerbations Revisited: Ventilation, Inflammation, Perfusion, and Structure (VIPS) Monitoring to Redefine Treatment
30. Novel outcome measures for clinical trials in cystic fibrosis
31. Quality improvement in your CF centre: taking care of care
32. Tracking CF disease progression with CT and respiratory symptoms in a cohort of children aged 6–19 years
33. Structural and Functional Lung Disease in Primary Ciliary Dyskinesia
34. Asthma and Cystic Fibrosis: A Tangled Web
35. Quantitative CT imaging analysis to predict pathology features in patients with a congenital pulmonary airway malformation.
36. Dose reduction for CT in children with cystic fibrosis: is it feasible to reduce the number of images per scan?
37. Small Airway Involvement in Cystic Fibrosis Lung Disease: Routine Spirometry as an Early and Sensitive Marker
38. Chest computed tomography scans should be considered as a routine investigation in cystic fibrosis
39. Aerosol therapy: The special needs of young children
40. New Antimicrobial Strategies in Cystic Fibrosis
41. Cystic Fibrosis Lung Disease Starts in the Small Airways: Can We Treat It More Effectively?
42. Tracheomalacia and Bronchomalacia in Children: Incidence and Patient Characteristics
43. Airway Dimensions in Bronchopulmonary Dysplasia:: Implications for Airflow Obstruction
44. Authorsʼ Reply
45. CT SCANS TO DETECT EARLY STRUCTURAL DAMAGE: S18.1
46. CF LUNG DISEASE: REVERSIBLE OR NON-REVERSIBLE, THAT IS THE QUESTION?: S2.4
47. Predictive Value of Infant Lung Function Testing for Airway Malacia
48. Small-airways deposition of dornase alfa in children with asthma and persistent airway obstruction
49. Extra-Fine Particles Improve Lung Delivery of Inhaled Steroids in Infants : A Study in an Upper Airway Model
50. DNase in stable cystic fibrosis infants: a pilot study
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