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2. P027This study presents a comprehensive genetic and clinical profiling of patients with cystic fibrosis ineligible for CFTR modulator therapy, offering insights from a diverse patient cohort

7. 135 Electronic home monitoring of children with cystic fibrosis to detect and treat acute pulmonary exacerbations and its effect on 1-year FEV1 loss

8. 505 Methicillin-resistant Staphylococcus aureus eradication rate increased after the initiation of a standardized regimen in children with cystic fibrosis

9. 307 Beneficial effects of breathing and relaxation exercises on psychological status, sleep, and quality of life of caregivers of children with cystic fibrosis

11. 86 Identifying Knowledge Gaps Using Adapted CF R.I.S.E in a Low Resource Setting

12. The effect of breathing exercise on the quality of life of 3-12 years old childrens with cystic fibrosis and their families

13. Respiratory functions in the follow-up of children with COVID-19 infection

14. P251 The effect of breathing exercises on the quality of life of 3- to 12-yearold patients with cystic fibrosis and their families

34. Predictors of complex aortic plaques in patients undergoing transeusophageal echocardiographic study

41. The role of unexplained high serum alpha-fetoprotein (AFP) and human chorionic gonadotropin (hCG) levels in the second trimester to determine poor obstetric outcomes [İkinci trimester maternal serumda açıklanamayan alfa feto protein (AFP) ve insan koryonik gonadotropin (hCG) yüksekliğinin olası gebelik komplikasyonlarını öngörmedeki rolü]

43. Oksijen Tedavisindeki Yenidoğanlarda Plazma Sistein Düzeyleri

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