Zobrazeno 1 - 10
of 86
pro vyhledávání: '"Saniye Ekinci"'
Autor:
İdil Rana User, Burak Ardıçlı, Arbay Özden Çiftçi, İbrahim Karnak, Berna Oğuz, Mithat Haliloğlu, Tezer Kutluk, Ferah Yıldız, Diclehan Orhan, Filiz Üzümcügil, Saniye Ekinci
Publikováno v:
Journal of Pediatric Research, Vol 11, Iss 2, Pp 118-122 (2024)
Aim: Malignant chest wall tumors are rare in children. We aimed to study the management of the Ewing family of tumors (EFT) in the chest walls of children. Materials and Methods: The files of patients diagnosed with primitive neuro-ectodermal tumor
Externí odkaz:
https://doaj.org/article/c9f0b147452040c1a98de063873d0216
Publikováno v:
Forbes Tıp Dergisi, Vol 3, Iss 2, Pp 160-164 (2022)
Objective: To assess the possible effect of hyperbaric oxygen (HBO) in preventing hypoxic-ischemic damage in cold-preserved organs. Methods: Visceral organs of white male New Zealand rabbits (n=6) were removed and examined in two groups: right kidney
Externí odkaz:
https://doaj.org/article/9cacc9c0364c481380f386683aa840f9
Autor:
Yagmur Unsal, Onur Gozmen, İdil Rana User, Hayriye Hızarcıoglu, Bora Gulhan, Saniye Ekinci, Tevfik Karagoz, Z. Alev Ozon, E. Nazlı Gonc
Publikováno v:
Frontiers in Endocrinology, Vol 14 (2023)
BackgroundCafé-au-lait skin macules, Cushing syndrome (CS), hyperthyroidism, and liver and cardiac dysfunction are presenting features of neonatal McCune–Albright syndrome (MAS), CS being the rarest endocrine feature. Although spontaneous resoluti
Externí odkaz:
https://doaj.org/article/fddd74a8905c4363b73098cb61da4ebc
Autor:
Doğuş Vurallı, Nazlı Gönç, Alev Özön, Saniye Ekinci, H. Serkan Doğan, Serdar Tekgül, Ayfer Alikaşifoğlu
Publikováno v:
JCRPE, Vol 14, Iss 1, Pp 17-28 (2022)
INTRODUCTION: Estrogen-secreting adrenocortical tumors (ACTs) are quite rare with feminizing adrenocortical tumors (FATs) accounting for 0.37-2% of all ACTs. The aim was to evaluate clinical and hormonal characteristics of FATS as well as treatment o
Externí odkaz:
https://doaj.org/article/bb59c52672de4ffba907c8c4fb618aa6
Autor:
H. Nursun Özcan, Özlem Özkale Yavuz, Saniye Ekinci, Berna Oguz, Tezer Kutluk, Mithat Haliloglu
Publikováno v:
Insights into Imaging, Vol 13, Iss 1, Pp 1-13 (2022)
Abstract Gastrointestinal (GI) tract tumors are rarely seen in children and adolescents, and can easily be misdiagnosed. Lymphoma is the most frequent GI tract tumor, and the common locations are ileum and ileocecal area. GI tract tumors may present
Externí odkaz:
https://doaj.org/article/66498f2395bf436f8dd3d0ba0ef0987f
Autor:
H. Nursun Özcan, Aziz Anil Tan, Burak Ardicli, Berna Oguz, Saniye Ekinci, Tezer Kutluk, Mithat Haliloglu
Publikováno v:
Diagnostic and Interventional Radiology, Vol 27, Iss 6, Pp 811-815 (2021)
Apart from neuroblastomas, adrenal tumors are rarely seen in children. The most common adrenal tumors are adrenocortical carcinoma and pheochromocytoma. Adrenocortical carcinoma is usually a large heterogeneous, well-marginated mass with solid/cystic
Externí odkaz:
https://doaj.org/article/a52fe32ec44e4f55b9961ca0651285e7
Autor:
Mutlu Uysal Yazici, Saniye Ekinci, Ozlem Keskin Turkmen, Ebru Gunes Yalcin, Arbay O. Ciftci, Safak Gucer, Diclehan Orhan, Ilhan Tezcan
Publikováno v:
European Journal of Pediatric Surgery Reports, Vol 02, Iss 01, Pp 038-042 (2014)
Abstract Split notochord syndrome is a rare group of developmental abnormalities caused by abnormal splitting or deviation of the notochord clinically resulting in the duplicated bowel associated with vertebral anomalies. We report on a case of 11-mo
Externí odkaz:
https://doaj.org/article/0e080234f1934e3091bcc7bb57fac9e9
Akademický článek
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Publikováno v:
Acta Medica. 53:356-361
Objective: Surgical exposure has utmost importance in the success of oncological surgery. Traditional incisions may not be adequate for exposure and total excision of the giant tumors. Thoracoabdominal incision favors excision of giant upper abdomina
Autor:
Burak Ardicli, Idil Rana User, Tunc Tigli, H. Nursun Ozcan, Berna Oguz, Mithat Haliloglu, Selman Kesici, Yasemin Ozsurekci, Ali Bulent Cengiz, Mehmet Ceyhan, Ilker Ertugrul, Saniye Ekinci
Publikováno v:
ANZ Journal of Surgery. 93:108-114
Abdominal pain is one of the most common symptoms of multisystem inflammatory syndrome in children (MIS-C). Abdominal pain can vary from mild to severe and may present as acute abdomen. Severe abdominal pain in patients with MIS-C should be different