Person: UZUNER, SELÇUK
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UZUNER
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SELÇUK
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- PublicationMetadata onlyAğır MTHFR Eksikliği Tanısında Metiyonin Düşüklüğünün Önemi(2017-04-30) TAŞ, İBRAHİM; CESUR, YAŞAR; UZUNER, SELÇUK; YEŞİL, GÖZDE; TAŞ, İBRAHİM; CESUR, YAŞAR; UZUNER, SELÇUK; YEŞİL, GÖZDE
- PublicationOpen AccessThe different cutaneous presentations in three cases of Kawasaki disease as confounding factor of diagnosis(2016-09-01) DEMIR, Aysegul Dogan; GOKNAR, Nilufer; Uzuner, SELÇUK; Vehapoglu, Aysel; Saritas, Turkay; OKTEM, Faruk; UZUNER, SELÇUK; VEHAPOĞLU TÜRKMEN, AYSELWe report three paediatric cases of Kawasaki disease (KD). Erythema multiforme (EM) was the presenting cutaneous feature in two patients, with young age (43 days old), macular rash and meningitis in the third patient. Diagnosis of KD was difficult due either to initial misdiagnosis of drug eruption, incomplete presentation, or the young age of the patient. Clinicians should be aware of these cutaneous presentations to prevent KD complications.
- PublicationMetadata onlyOlgu Sunumu: HAİR-AN sendromu(2012-05-19) ÖZGEN, İLKER TOLGA; CESUR, YAŞAR; UZUNER, SELÇUK; ÖZGEN, İLKER TOLGA; CESUR, YAŞAR; UZUNER, SELÇUK
- PublicationMetadata onlyhafif kistik fibrozisli çocuk hastalarda sağ kalp fonksiyonlarının değerlendirilmesi(2018-04-12T00:00:00Z) Gulieva, Aynur; Yozgat, Yılmaz; Çakır, Erkan; Otçu Temur, Hafize; Erenberk, Ufuk; Uzuner, Selçuk; Al Shadfan, Lina Muhammed; Yakut, Kahraman; YOZGAT, YILMAZ; ÇAKIR, ERKAN; OTÇU TEMUR, HAFİZE; ERENBERK, UFUK; UZUNER, SELÇUK; YAKUT, KAHRAMAN
- PublicationMetadata onlyİLERLEYİCİ ŞİLOTORAKS GELİŞEN VE SİROLİMUS TEDAVİSİNE CEVAP VEREN BİR GORHAM-STOUT SENDROMU(2017-04-23) ÇAKIR, FATMA BETÜL; Uzuner, SELÇUK; Khalif, Fatouma; Akdemir, Cemil; Ziyade, SEDAT; Kutlu, Onur Nurettin; ÇAKIR, FATMA BETÜL; UZUNER, SELÇUK; ZİYADE, SEDAT
- PublicationMetadata onlyA Rare Presentation of Neurobrucellosis in a 6-Year-Old Pediatric Patient with Sagittal Sinus Thrombosis(2020-10-01T00:00:00Z) TÜREL, Özden; KUTLU, NURETTİN ONUR; YEŞİLBAŞ, Osman; Yozgat, Can Yilmaz; DÜNDAR, TOLGA TURAN; BURSAL DURAMAZ, BURCU; UZUNER, SELÇUK; ABDİLLAHİ, FATOUMA KHALİF; TÜREL, ÖZDEN; UZUNER, SELÇUK; BURSAL DURAMAZ, BURCU; DÜNDAR, TOLGA TURAN; SEYİTHANOĞLU, MEHMET HAKAN; YEŞİLBAŞ, OSMAN; KUTLU, NURETTİN ONURBrucellosis is one of the most common zoonosis worldwide. It is still endemic in many regions of the world. A 6-year-old female was admitted to the emergency department (ED) due to a sudden change in consciousness, urinary incontinence, vomiting, and difficulty in walking. Neurological examination demonstrated abducens nerve paralysis, mild-to-moderate motor deficit in hemiparesis in the left arm. Brain magnetic resonance imaging showed a hemorrhagic focus at the right frontal lobe and thrombosis in the superior sagittal sinus of the brain. The diagnosis of neurobrucellosis was confirmed by identifying Brucella spp. in the blood culture on the day 6 of pediatric intensive care unit admission; thus, trimethoprim-sulfamethoxazole and rifampicin, and ceftriaxone were promptly initiated. Despite neuroprotective management and acetazolamide, the patient-s neurological problems and high intracranial pressure (ICP) persisted. An external ventricular drainage tube and a Codman ICP monitor were placed to be on the consent vigilance of the patient-s neurological condition. The patient-s ICP continued to increase despite the current treatment regimen; therefore, a decompressive bitemporal craniectomy was performed. The ICP level of the patient returned to its normal range immediately after the craniectomy. The patient did not have any notable neurologic sequelae at the first-year follow-up. Neurobrucellosis is a rare complication of systemic brucellosis and may present as meningitis, encephalitis, myelitis, radiculitis, and/or neuritis. Herein, we describe a six-year-old girl with brucellosis complicated with cerebral vein thrombosis. This case illustrates the need for close monitoring of patients with unexplained neurological signs or symptoms for brucellosis in endemic areas.
- PublicationMetadata onlyA 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, ERKAN
- PublicationMetadata onlyEvaluation 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.
- PublicationMetadata onlyAssociation 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.
- PublicationMetadata onlyÇocuk yaş gurubunda Vİdeo Yardımlı Torakoskopik Cerrahi uygulamalarımız(2021-12-04T00:00:00Z) Kök, Abdülaziz; Ceyhan, Süleyman; Yazan, Hakan; Çakır, Erkan; AKDEMİR, OSMAN CEMİL; KÖK, ABDÜLAZİZ; CEYHAN, SÜLEYMAN; UZUNER, SELÇUK; ÇAKIR, ERKAN