24 results on '"de Boeck, K"'
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2. Expression of soluble triggering receptor expressed on myeloid cells-1 in childhood CF and non-CF bronchiectasis
3. Hemoptysis after orthopedic surgery in an adolescent boy
4. EFFICACY AND SAFETY BY AGE GROUP FROM THE PHASE III STUDIES OF BRONCHITOL (INHALED MANNITOL) IN PATIENTS WITH CF: 236
5. MODIFIED NASAL CATHETER FOR MEASUREMENT OF NASAL POTENTIAL DIFFERENCE IMPROVES REPRODUCIBILITY: 218
6. Montelukast does not prevent reactive airway disease in young children hospitalized for RSV bronchiolitis
7. ‘Difficult Asthma’: Can Symptoms be Controlled in a Structured Environment?
8. Phenotypic characterisation of patients with intermediate sweat chloride values: towards validation of the European diagnostic algorithm for cystic fibrosis
9. CHILDREN WITH NONSENSE-MUTATION-MEDIATED CYSTIC FIBROSIS RESPOND TO INVESTIGATIONAL TREATMENT WITH PTC124: 316
10. A COMPARISON OF METHODS USED FOR NASAL POTENTIAL DIFFERENCE MEASUREMENT IN EUROPEAN CF CENTERS: TOWARDS A STANDARD OPERATING PROCEDURE: 231
11. MUTATIONS IN THE AMILORIDE-SENSITIVE EPITHELIAL SODIUM CHANNEL IN PATIENTS WITH CYSTIC FIBROSIS-LIKE DISEASE: 205⋆
12. ANALYSIS OF THE GENES CODING FOR THE AMILORIDE SENSITIVE EPITHELIAL SODIUM CHANNEL AS MODIFIER GENES FOR CYSTIC FIBROSIS: 206
13. Type III IFN-λ mRNA expression in sputum of adult and school-aged asthmatics
14. Role of magnesium in the failure of rhDNase therapy in patients with cystic fibrosis
15. NEWLY ACQUIRED PSEUDOMONAS AERUGINOSA IN BELGIAN CYSTIC FIBROSIS PATIENTS: DOES THE PATIENTSʼ P. AERUGINOSA GENOTYPE CORRELATE WITH THE ENVIRONMENTAL GENOTYPES?: 325
16. Cystic fibrosis: terminology and diagnostic algorithms
17. Mucociliary transport using 99mTc-albumin colloid: a reliable screening test for primary ciliary dyskinesia
18. Association of tumour necrosis factor alpha variants with the CF pulmonary phenotype
19. Polymorphisms in the mannose binding lectin gene affect the cystic fibrosis pulmonary phenotype
20. Efficacy and Safety of Oral Fludarabine Phosphate in Previously Untreated Patients With Chronic Lymphocytic Leukemia
21. Evolution of primary resistance in Belgium (1995–2000)
22. Evaluating fat malabsorption in children with cystic fibrosis: comparing the13 C-mixed triglyceride breath test with the 72 hour faecal fat collection
23. Lipid digestion in cystic fibrosis: comparison of conventional and high lipase enzyme therapy using the mixed triglyceride breath test
24. Respiratory Syncytial Virus Infection in Infants with Unequal Pulmonary Perfusion
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