30 results on '"Cirilli, N."'
Search Results
2. Real life practice of sweat testing in Europe
3. A randomized placebo-controlled study on high-dose oral algal docosahexaenoic acid supplementation in children with cystic fibrosis
4. P040 Sweat chloride values in cystic fibrosis patients after one year on elexacaftor/tezacaftor/ivacaftor
5. P207 Spirometric values and 6-minute walking distance in cystic fibrosis patients on elexacaftor/texacaftor/ivacaftor
6. P162 Body composition assessment in cystic fibrosis (CF) patients on elexacaftor/texacaftor/ivacaftor
7. P129 Evidence for a role of Achromobacter xylosoxidans VBNC forms in chronic cystic fibrosis lung infection
8. P113 Microbiology assessment in cystic fibrosis patients on elexacaftor/tezacaftor/ivacaftor
9. P032 Sweat chloride values in cystic fibrosis patients on elexacaftor/tezacaftor/ivacaftor
10. P020 CFTR mutation panel in detecting cystic fibrosis screen positive inconclusive diagnosis patients (CFSPIDs) in the Marche Region, Italy
11. P007 A novel cystic fibrosis-causing mutation identified in a newborn of African origin
12. P029 Validation of new sweat test control materials
13. P005 Lessons from 5T;TG12
14. P278 Cataloguing outcome measures of cystic fibrosis clinical studies
15. 428 Are cystic fibrosis guidelines credible? Evaluating methodological issues
16. 111 Non-tuberculous mycobacteria in patients with cystic fibrosis: detection and isolation from respiratory samples. Results of a cross-sectional study
17. WS10.6 Intra-individual biological variation in sweat chloride concentrations
18. WS11.4 Real life practice of sweat testing in Europe: results from an ECFS-wide survey
19. 62 Molecular diagnosis of Pseudomonas aeruginosa infection in culture-negative samples from cystic fibrosis patients
20. 281 Patient-centered outcomes in CF research
21. 282 Patient priorities for research in cystic fibrosis: the IPaCOR experience
22. 26 Risk factors for poor outcomes in cystic fibrosis newborns diagnosed by neonatal screening in Italy: years 2009–2011
23. 10 The role of complex alleles in patients with cystic fibrosis and L997F
24. WS21.3 Clinical variability in patients with cystic fibrosis and D1152H mutation
25. 20 Cystic fibrosis newborn screening in Italy: survey for assessment of technical-scientific and organizational issues
26. 290 Oral DHA supplementation in children with cystic fibrosis: a randomized placebo-controlled study
27. EMERGENCE OF COLISTIN-RESISTANT PSEUDOMONAS AERUGINOSA FROM ITALIAN CYSTIC FIBROSIS PATIENTS
28. Pseudomonas aeruginosa (PA) resistant to colistin (CL) in Italian cystic fibrosis (CF) patients
29. 110 Genetic fingerprinting of Pseudomonas aeruginosa (PA) from Italian CF patients (pts): comparison with isolates from environment and other clinical origins in Europe
30. 73* Occurrence of P. aeruginosa (PA) with hypermutable phenotype (HPM) in Italian CF patients
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