198 results on '"A Bourke"'
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2. The natural history of cystic fibrosis liver disease a prospective cohort study
3. Factors associated with clinical progression to severe COVID-19 in people with cystic fibrosis: A global observational study
4. Using a learning health system to understand the mismatch between medicines supply and actual medicines use among adults with cystic fibrosis
5. The impact of liver disease on mortality in cystic fibrosis–A systematic review
6. P414 Providing advice and information to women with cystic fibrosis on their reproductive choices
7. P379 “Now I have a future”: adult perspectives and experiences of health status and adherence post CFTR modulator therapy
8. P441 Virtualwards for providing hospital-at-home care for adults with cystic fibrosis
9. Monitoring of ECFS quality standards for the clinical management of adults with cystic fibrosis
10. Ivacaftor and symptoms of extra-oesophageal reflux in patients with cystic fibrosis and G551D mutation
11. The natural history of cystic fibrosis liver disease a prospective cohort study
12. A novel culture medium for isolation of rapidly-growing mycobacteria from the sputum of patients with cystic fibrosis
13. Corrigendum to 'Using a learning health system to understand the mismatch between medicines supply and actual medicines use among adults with cystic fibrosis' [J Cyst Fibros (2022), 21/2, 323-331]
14. P289 Intestinal obstruction syndromes in cystic fibrosis
15. P147 “What options are available for those not able to take current CFTR modulators?”: an answer hidden in plain sight?
16. P282 Implementing routine assessment of gastrointestinal outcome measures in the cystic fibrosis clinic
17. P427 Evaluating the provision of exercise for in-patients with cystic fibrosis across cystic fibrosis centres in the UK and identification of challenges and barriers surrounding delivery of care
18. EPS2.09 Cervical cancer in cystic fibrosis: from treatment to prevention
19. Outcome in patients with cystic fibrosis liver disease
20. The impact of switching to the new global lung function initiative equations on spirometry results in the UK CF Registry
21. Elexacaftor-Tezacaftor-Ivacaftor improve Gastro-Oesophageal reflux and Sinonasal symptoms in advanced cystic fibrosis
22. Corrigendum to “Using a learning health system to understand the mismatch between medicines supply and actual medicines use among adults with cystic fibrosis” [J Cyst Fibros (2022), 21/2, 323-331]
23. Factors associated with clinical progression to severe COVID-19 in people with cystic fibrosis: A global observational study
24. WS04.06 Neoplastic disease and treatment in cystic fibrosis (CF): a comprehensive single centre case series
25. P200 The prevalence of laryngopharyngeal reflux and sino-nasal symptoms in adults with cystic fibrosis
26. The global impact of SARS-CoV-2 in 181 people with cystic fibrosis
27. WS04.06 Neoplastic disease and treatment in cystic fibrosis (CF): a comprehensive single centre case series
28. P200 The prevalence of laryngopharyngeal reflux and sino-nasal symptoms in adults with cystic fibrosis
29. P182 Prevalence of tracheobronchomalacia is higher than previously reported in children with cystic fibrosis
30. WS11.05 Medication burden among adults with cystic fibrosis prescribed CFTR Modulators: a cross-sectional survey
31. P077 Clinical factors affecting timing of referral for lung transplantation for people with cystic fibrosis: a national comparison of opinions between adult cystic fibrosis and transplant centres
32. P042 RECOVER - the Real World Clinical Outcomes with Novel Modulator therapy combinations in people with cystic fibrosis
33. P079 Using a learning health system to understand medicine waste in cystic fibrosis – the Easy Medicines for Burden Reduction And Care Enhancement (EMBRACE) study
34. The global impact of SARS-CoV-2 in 181 people with cystic fibrosis
35. P350 Bereavement: a ‘time to remember’ event for families bereaved by cystic fibrosis
36. P077 Clinical factors affecting timing of referral for lung transplantation for people with cystic fibrosis: a national comparison of opinions between adult cystic fibrosis and transplant centres
37. P042 RECOVER - the Real World Clinical Outcomes with Novel Modulator therapy combinations in people with cystic fibrosis
38. P079 Using a learning health system to understand medicine waste in cystic fibrosis – the Easy Medicines for Burden Reduction And Care Enhancement (EMBRACE) study
39. P350 Bereavement: a ‘time to remember’ event for families bereaved by cystic fibrosis
40. WS12-6 Evaluating appropriate PROMs in CARE-CF-1 trial: Lynovex® (cysteamine) an oral adjunct to SOC interventions in cystic fibrosis infectious exacebations
41. WS18-3 Is “Pactster” an acceptable tool to promote exercise participation in the adult cystic fibrosis community, with and without physiotherapy support?
42. WS12-6 Evaluating appropriate PROMs in CARE-CF-1 trial: Lynovex® (cysteamine) an oral adjunct to SOC interventions in cystic fibrosis infectious exacebations
43. P167 Microbiological characteristics of cystic fibrosis patients colonised with Exophiala dermatitidis in a regional centre
44. P044 Clinical characteristics, gender differences and outcomes in adult-diagnosed cystic fibrosis and Cystic Fibrosis-Related disorders (CFRD)
45. P044 Clinical characteristics, gender differences and outcomes in adult-diagnosed cystic fibrosis and Cystic Fibrosis-Related disorders (CFRD)
46. P167 Microbiological characteristics of cystic fibrosis patients colonised with Exophiala dermatitidis in a regional centre
47. P244 Fertility and fatherhood in men with cystic fibrosis (CF)
48. WS12.3 Telehealth monitoring for home intravenous antibiotics in cystic fibrosis
49. IPD1.08 Treating unresolved grief in parents of children with cystic fibrosis
50. 108 RGM: A new medium for isolation of rapidly-growing mycobacteria from respiratory samples of patients with cystic fibrosis: 15 months' experience of routine use for CF respiratory samples
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