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2. P140 This abstract is a study that investigates demographic and anthropometric changes, the relationship between variables and survival analyses of people with cystic fibrosis by years

3. P114 Social determinants of health in cystic fibrosis

9. 422 Outcomes of patients with intermittent versus continuous access to CFTR modulator therapy in Turkey

10. 640 Cystic fibrosis transition program (CF RISE) translated to Turkish (KF SOBE): first annual results

11. 435 Outcomes of cessation of CFTR modulator therapy: an unfortunate experience

13. P223 Transition programme as a quality improvement project: adaptation of the R.I.S.E. in a centre with limited resources – Marmara University experience

14. Improvement of Lung Function After Implementation of Standardized Cystic Fibrosis Care Algorithm: Quality Improvement Project-International Collaboration

16. The association between the cumulative dose of aminoglycoside exposure and hearing loss in children with cystic fibrosis

17. Home mechanical ventilation in children: The experience of pediatric pulmonology divisions in Istanbul

18. Otologic features in patients with Primary Ciliary Dyskinesia- an EPIC-PCD study

20. Sinonasal features in patients with Primary Ciliary Dyskinesia - an EPIC-PCD study

22. Otologic features in patients with Primary Ciliary Dyskinesia – an EPIC-PCD study

23. Task Force report: European Respiratory Society statement for defining respiratory exacerbations in children and adolescents with bronchiectasis for clinical trials

26. WS07.04 Electronic home monitoring of children with cystic fibrosis to detect and treat acute pulmonary exacerbations and their effect on one year FEV1 loss

27. P149 The association between the cumulative dose of aminoglycoside exposure and hearing loss in children with cystic fibrosis

31. 108: Change in FEV1 after implementation of standardized CF care algorithm: A quality improvement project

32. 109: Implementation of standardized nutritional algorithm increased the body mass index of children with cystic fibrosis: Quality improvement project

39. First analysis of the Severe Paediatric Asthma Collaborative in Europe registry

40. First analysis of the Severe Paediatric Asthma Collaborative in Europe registry

43. WS10.1 Change in body mass index of children with cystic fibrosis after a standardised nutritional algorithm – a quality improvement project

44. P098 Change in FEV1 after standardised care algorithm for cystic fibrosis patients: quality improvement project

47. P121 The effect of training about nebuliser cleaning and disinfection on the knowledge levels and practises of the caregivers of patients with cystic fibrosis

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