Person: UZUNER, SELÇUK
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Publication Metadata only CINCA syndrome in an infant presenting with hydrocephalus.(2014-03-01) TUREL, O; GOKNAR, N; Uzuner, SELÇUK; KASAPCOPUR, O; CUISSET, L; TÜREL, ÖZDEN; UZUNER, SELÇUKPublication Metadata only Lorazepam in the treatment of posttraumatic feeding disorder.(2014-06-01T00:00:00Z) KARDAS, M; CERMIK, BB; EKMEKCI, S; Uzuner, SELÇUK; GOKCE, S; UZUNER, SELÇUKPublication Metadata only ; Information Quality on Developmental Dysplasia of the Hip on Turkish Websites(2016-08-01T00:00:00Z) Ceylan, Hasan Huseyin; Caypinar, Baris; Kucukkoc, Mehmet; UZUNER, SELÇUK; KÜÇÜKDURMAZ, FATİH; UZUNER, SELÇUK; KÜÇÜKDURMAZ, FATİHObjective: We aimed to evaluate the reliability of Turkish information achieved from websites about developmental dysplasia of the hip using standardized scientific methods.Publication Metadata only Nontuberculous pulmonary cavitary diseases of childhood.(2015-03-01T00:00:00Z) Cakir, Erkan; Gedik, AH; Ari, E; Ozdemir, A; Cakir, FATMA BETÜL; Bilgin, M; Ziyade, S; ÇAKIR, ERKAN; ÇAKIR, FATMA BETÜL; UZUNER, SELÇUK; BİLGİN, MEHMETPublication Metadata only Bone mineral density and associated parameters in pre-pubertal children with asthma treated with long-term fluticasone propionate.(2013-03-01) OZKAYA, EMİN; Çakır, ERKAN; UZUNER, SELÇUK; ERENBERK, UFUK; DUNDARÖZ, MR; ÖZKAYA, EMİN; ÇAKIR, ERKAN; UZUNER, SELÇUK; ERENBERK, UFUKPublication Metadata only Lokal Anestezik Uygulamasının Ender Bir Komplikasyonu: Methemoglobinemi(2013-11-01) UZUNER, SELÇUK; Küçükkoç, Mehmet; TORUN, EMEL; KARDAS, M; GOKCE, S; UZUNER, SELÇUK; TORUN, EMELPublication Metadata only Skin temperature measurement using an infrared thermometer on patients who have been exposed to cold.(2013-12-01) ERENBERK, UFUK; TORUN, EMEL; OZKAYA, EMİN; Uzuner, SELÇUK; DEMIR, AD; DUNDAROZ, R; ERENBERK, UFUK; TORUN, EMEL; ÖZKAYA, EMİN; UZUNER, SELÇUKPublication Metadata only A pediatric case of factitious disorder with unexplained bleeding symptoms.(2013-11-01) UZUNER, SELÇUK; BAHALI, K; KURBAN, S; ERENBERK, UFUK; Cakir, ERKAN; UZUNER, SELÇUK; ERENBERK, UFUK; ÇAKIR, ERKANPublication Metadata only Evaluation of Autonomic Nervous System function in Children with Overactive Bladder Syndrome(2017-03-01) DEMIR, Aysegul Dogan; Gursoy, AZİZE ESRA; GOKNAR, Nilufer; Uzuner, SELÇUK; Ozkaya, EMİN; Erenberk, UFUK; Vehapoglu, Aysel; DUNDAROZ, Mehmet Rusen; OKTEM, Faruk; GÜRSOY, AZIZE ESRA; UZUNER, SELÇUK; ÖZKAYA, EMİN; ERENBERK, UFUK; VEHAPOĞLU TÜRKMEN, AYSELPurpose We aimed to evaluate the autonomic nervous system activity in children with overactive bladder (OAB) syndrome.Methods Included in the study were 40 children with overactive bladder and 28 healthy controls. Autonomic tests were performed on all participants, including heart rate interval variation (RRIV), heart rate response to valsalva maneuver, and sympathetic skin response (SSR).Results Mean valsalva rates in the overactive bladder and control groups were 1.530.29 and 1.30 +/- 0.18, respectively, a statistically significant difference (P0.05).Conclusions This study demonstrated a parasympathetic hyperactivity in children with OAB, results suggesting a dysfunction in their autonomic nervous systems. (C) 2016 Wiley Periodicals, Inc.Publication Metadata only Association between myeloperoxidase gene polymorphism and familial mediterranean fever in Turkish Children(2016-01-01) DEMIR, Aysegul Dogan; GOKNAR, Nilufer; OKTEM, Faruk; Ergen, Hayriye Arzu; Dogan, Akif Nuri; Uzuner, SELÇUK; Vehapoglu, Aysel; Yazici, MEBRURE; UZUNER, SELÇUK; VEHAPOĞLU TÜRKMEN, AYSEL; YAZICI, MEBRUREBackground: Familial Mediterranean Fever (FMF) is the most common autoinflammatory disease. Autoinflammatory disorders are characterized by exaggerated immune system responses. Neutrophils and their byproduct, myeloperoxidase, are important components of the innate immune system. In the present study, we searched for myeloperoxidase gene polymorphisms in FMF patients. Methodology/Principal Findings: We evaluated 83 children diagnosed with FMF by their physicians and 93 controls without any family history of FMF. MPO gene polymorphisms were detected using polymerase chain reaction (PCR)-based methods. We genotyped all samples in terms of the -463G/A single-nucleotide polymorphism, the most extensively studied MPO polymorphism. Allelic and genotypic frequencies were calculated, and possible associations with FMF explored. The frequencies of MPO polymorphisms differed significantly between the study and control groups (P = 0.003). The AA and AG gene polymorphisms were more prevalent in the FMF group than in the controls. The A allele was more prevalent in the FMF group (P = 0.001), and the frequency of the G allele was similar between the two groups (P = 0.128). Conclusion: MPO gene polymorphisms and allelic differences may be important in the pathogenesis of FMF.