Zobrazeno 1 - 10
of 13
pro vyhledávání: '"Evrim Özmen"'
Autor:
Mine Aslan, Ahmet Aslan, Hatice Arıöz Habibi, Ayşe Kalyoncu Uçar, Evrim Özmen, Selim Bakan, Sebuh Kuruğoğlu, İbrahim Adaletli
Publikováno v:
Diagnostic and Interventional Radiology, Vol 23, Iss 5, Pp 403-406 (2017)
PURPOSE:Wilms tumor (WT) and neuroblastoma (NB) are the most common pediatric abdominal malignant neoplasms of the kidney and adrenal gland. Differentiating them from each other is essential since their treatments are different. Here, we aimed to sho
Externí odkaz:
https://doaj.org/article/3d17717edec9486998c675275bc09763
Publikováno v:
Balkan Medical Journal, Vol 33, Iss 3, Pp 275-282 (2016)
Background: Contrast enhanced magnetic resonance cholangiography is a novel technique and promising method in demonstrating biliary tree anatomy and evaluating biliary disorders. However, to date, there are a limited number of studies that have focus
Externí odkaz:
https://doaj.org/article/8b2ebe06957f4095bde324a67b6526e5
Autor:
Evrim Özmen, Betül Derinkuyu, Cesur Samancı, Havva Akmaz Ünlü, Tülin Hakan Demirkan, Zehra Işık Haşıloğlu, Sebuh Kuruoğlu, İbrahim Adaletli
Publikováno v:
Diagnostic and Interventional Radiology, Vol 21, Iss 3, Pp 256-261 (2015)
PURPOSEWe aimed to examine whether the brain displays any microstructural changes after a three-week Ramadan fasting period using diffusion tenson imaging.METHODSThis study included a study and a control group of 25 volunteers each. In the study grou
Externí odkaz:
https://doaj.org/article/443ab88b6de44f9187cfcfc17629af2f
Publikováno v:
Haseki Tıp Bülteni, Vol 52, Iss 1, Pp 60-63 (2014)
Uterovaginal duplication with imperforated hemivagina is a rare type of Mullerian anomaly. If ipsilateral renal agenesis is associated with this complex genital malformation, it is called Herlyn-Werner-Wunderlich syndrome. Clinical presentations of t
Externí odkaz:
https://doaj.org/article/4ad50ff2615241ada09ec0df057239f6
Autor:
Yasemin Kayadibi, Deniz Çebi Olgun, Evrim Özmen, Rahşan Özcan, Afşin İpekçi, İbrahim İkizceli
Publikováno v:
Eurasian Journal of Emergency Medicine, Vol 13, Iss 4, Pp 204-205 (2014)
An amulet with a blue bead and metal coin are the most common causes of foreign body ingestion in childhood in Turkey. There are few case reports of metal spoons ingested in the literature. In this case report, our aim is to report a teaspoon that wa
Externí odkaz:
https://doaj.org/article/c0ce337204c841e78aba8418273f9941
Publikováno v:
Journal of Academic Research in Medicine. 10:94-96
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0f5594db0465d83aef44bdd02478bca2
https://doi.org/10.4274/jarem.galenos.2018.2401
https://doi.org/10.4274/jarem.galenos.2018.2401
Autor:
Sukru Mehmet Erturk, Evrim Özmen
Publikováno v:
Medical Imaging Contrast Agents: A Clinical Manual ISBN: 9783030792558
In pediatric patients, most widely used imaging tools are ultrasonography, magnetic resonance imaging, fluoroscopy, and computed tomography, respectively. Each of these modalities requires contrast materials compatible with the modality and imaging g
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::80d08c16193cd4ff5f2458c208f51f7b
https://doi.org/10.1007/978-3-030-79256-5_20
https://doi.org/10.1007/978-3-030-79256-5_20
Publikováno v:
Journal of Pediatric Neurology. 17:176-179
Pituitary stalk interruption syndrome is a congenital anomaly characterized by interrupted or thin pituitary stalk, hypoplastic or absent anterior pituitary, and an absent or ectopic posterior pituitary gland. The exact incidence rate of this syndrom
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::734ebb219efb8e5c28517c59f2e23ad6
https://doi.org/10.1055/s-0038-1661412
https://doi.org/10.1055/s-0038-1661412
Autor:
Ferda Alparslan Pinarli, Aylin Yetim, Banu Yılmaz Özgüven, Evrim Özmen, Ahmet Uçar, Muharrem Battal, Yasin Yilmaz
Publikováno v:
Journal of Clinical Research in Pediatric Endocrinology
Multiple endocrine neoplasia (MEN1) is a rare autosomal dominant disorder characterized by primary hyperparathyroidism, enteropancreatic neuroendocrine tumors, and anterior pituitary adenomas. A 16-year-old male presented to the emergency outpatient
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::db45aa61e9b56f294cfbd7ae8154f219
https://doi.org/10.4274/jcrpe.4799
https://doi.org/10.4274/jcrpe.4799
Autor:
Selcen Bozkurt, Ayse Merve Usta, Nafiye Urganci, Nida Gulderen Kalay, Gulsen Kose, Evrim Ozmen
Publikováno v:
BMC Pediatrics, Vol 22, Iss 1, Pp 1-5 (2022)
Abstract Background Coats plus syndrome, cerebroretinal microangiopathy with calcifications and cysts, is a rare disease with autosomal recessive pattern occurring due to a mutation in CTC1, encoding conserved telomere maintenance component 1, gene.
Externí odkaz:
https://doaj.org/article/ded3f46f8c144650a60677018b66dfb9