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Özcan-Ekşi Emel Ece,Canbolat Çağrı,Ayhan Selim,Ekşi Murat Şakir 대한척추외과학회 2020 Asian Spine Journal Vol.14 No.5
Study Design: This is a cross-sectional study of literature databases.Purpose: The purpose of this study is to analyze the predictive factors for the publication rates of spine studies.Overview of Literature: Spine research has garnered worldwide interest due to the increased number of spinal disorders in aging population.Methods: We evaluated the abstracts presented at the annual meetings of the Spine Society of Europe between 2009 and 2012. Additionally, we recorded presentation categories, study designs, research types, random assignments of the subjects, single- or multi-center- based methodologies, and significance of the results.Results: We evaluated 965 abstracts, 53.5% of which were published in peer-reviewed journals. Publication rates were significantly higher for oral presentations (62.9%) and prospective studies (61.3%) as compared to the poster presentations (46.7%) and retrospective studies (44.2%), respectively (p <0.001). Clinical studies contributed to about 86.1% of the published abstracts. However, publication rates were significantly higher for laboratory studies as compared to clinical studies (70.1% vs. 50.8%, p <0.001). Multi-center studies were closer to publication than single-center studies (67.1% vs. 52.2%, p =0.009). Our study demonstrated that multi-center studies (odds ratio, 1.81; p =0.016) and laboratory studies (odds ratio, 2.60; p <0.001) are more likely to be published.Conclusions: Multi-center collaborations dedicated to experimental studies in spine research are highly ranked and more likely to be published in peer-reviewed journals.
Cystic fibrosis of pancreas and nephrotic syndrome:a rare association
Selvi Kelekçi,Müsemma Karabel,Aydın Ece,Velat Şen,Ali Güneş,İlyas Yolbaş 대한소아청소년과학회 2013 Clinical and Experimental Pediatrics (CEP) Vol.56 No.10
Cystic fibrosis (CF) is a genetic disease with autosomal recessive inheritance and is common in Caucasian people. The prevalence of this disease is between 1/2,000 and 1/3,500 live births, and the incidence varies between populations. Although the CF transmembrane conductance regulator gene is expressed in the kidneys, renal involvement is rare. With advances in the treatment of CF, life expectancy has increased, and some previously unobserved disease associations are now seen in patients with CF. It is important to follow patients with CF for possible abnormalities that may accompany CF. In this paper, we present two rare cases of CF accompanied by nephrotic syndrome.