Zobrazeno 1 - 10
of 31
pro vyhledávání: '"Zeynep Siklar"'
Autor:
Zeynep Şıklar, Elif Özsu, Sirmen Kızılcan Çetin, Samim Özen, Filiz Çizmecioğlu-jones, Hanife Gül Balkı, Zehra Aycan, Damla Gökşen, Fatih Kilci, Sema Nilay Abseyi, Ummahan Tercan, Gözde Gürpınar, Şükran Poyrazoğlu, Feyza Darendeliler, Korcan Demir, Özge Besci, İlker Tolga Özgen, Semra Bahar Akın, Zümrüt Kocabey Sütçü, Emel Hatun Aykaç Kaplan, Emine Çamtosun, İsmail Dündar, Elif Sağsak, Hüseyin Anıl Korkmaz, Ahmet Anık, Gül Yeşiltepe Mutlu, Bahar Özcabı, Ahmet Uçar, Aydilek Dağdeviren Çakır, Beray Selver Eklioğlu, Birgül Kırel, Merih Berberoğlu
Publikováno v:
JCRPE, Vol 16, Iss 3, Pp 288-296 (2024)
INTRODUCTION: Craniopharyngiomas (CPG) have complex treatment challenges due to their proximity to vital structures, surgical and radiotherapeutic complexities, and the tendency for recurrence. The aim of this study was to identify the prevalence of
Externí odkaz:
https://doaj.org/article/6b8a9e21a0b84e9e8ec5bc2a07ecc15e
Autor:
Elif Özsu, Semra Çetinkaya, Semih Bolu, Nihal Hatipoğlu, Şenay Savaş Erdeve, Olcay Evliyaoğlu, Firdevs Baş, Atilla Çayır, İsmail Dündar, Emine Demet Akbaş, Seyid Ahmet Uçaktürk, Merih Berberoğlu, Zeynep Şıklar, Şervan Özalkak, Nursel Muratoğlu Şahin, Melikşah Keskin, Ülkü Gül Şiraz, Hande Turan, Ayşe Pınar Öztürk, Eda Mengen, Elif Sağsak, Fatma Dursun, Nesibe Akyürek, Sevinç Odabaşı Güneş, Zehra Aycan
Publikováno v:
JCRPE, Vol 16, Iss 3, Pp 297-305 (2024)
INTRODUCTION: Maturity onset diabetes of the young (MODY) occurs due to mutations in genes involved in pancreatic beta cell function and insulin secretion, has heterogeneous clinical and laboratory features, and account for 1-5% of all diabetes cases
Externí odkaz:
https://doaj.org/article/eb7e190aaeb24a0bb6a30c654ca0303b
Autor:
Sirmen Kızılcan Çetin, Zehra Aycan, Zeynep Şıklar, Serpil Dizbay Sak, Serdar Ceylaner, Elif Özsu, Merih Berberoğlu
Publikováno v:
JCRPE, Vol 16, Iss 3, Pp 340-343 (2024)
Dyshormonogenesis (DG) is the failure of thyroid hormone production due to a defect in thyroid hormonogenesis. Loss-of-function mutations in the thyroglobulin (TG) gene are a cause of DG, leading to gland stimulation by thyroid-stimulating hormone (T
Externí odkaz:
https://doaj.org/article/a7499a12f8f54d129edfa78fb16675da
Autor:
Sirmen Kızılcan Çetin, Zehra Aycan, Elif Özsu, Zeynep Şıklar, Ayşegül Ceran, Seda Erişen Karaca, Gizem Şenyazar, Merih Berberoğlu
Publikováno v:
JCRPE, Vol 15, Iss 3, Pp 230-237 (2023)
INTRODUCTION: Abnormal uterine bleeding (AUB) is the most common gynecologic complaint in adolescent girls. The aim of this study was to identify the diagnostic and management differences between those with/without heavy menstrual bleeding. METHODS:
Externí odkaz:
https://doaj.org/article/b15f54126de34c9588004f24e8f08092
Autor:
Fevzi Kahveci, Buse Önen Ocak, Emrah Gün, Anar Gurbanov, Hacer Uçmak, Ayşen Durak Aslan, Ayşegül Ceran, Hasan Özen, Burak Balaban, Edin Botan, Zeynep Şıklar, Merih Berberoğlu, Tanıl Kendirli
Publikováno v:
Acute and Critical Care, Vol 38, Iss 3, Pp 371-379 (2023)
Background Diabetic ketoacidosis (DKA) is a common endocrine emergency in pediatric patients. Early presentation to health facilities, diagnosis, and good management in the pediatric intensive care unit (PICU) are crucial for better outcomes in child
Externí odkaz:
https://doaj.org/article/640c7a411d33402aa4db2f143c7c8545
Publikováno v:
JCRPE, Vol 15, Iss 1, Pp 90-96 (2023)
The tRNA methyltransferase 10 homologue A (TRMT10A) gene encodes tRNA methyl transferase, and biallelic loss of function mutations cause a recessive syndrome of intellectual disability, microcephaly, short stature and diabetes. A case with intellectu
Externí odkaz:
https://doaj.org/article/8e23ceaaf634424fa9d430fd08ba14f4
Autor:
Sirmen Kızılcan Çetin, Mehmet Gökhan Ramoğlu, Zeynep Şıklar, Elif Özsu, Zehra Aycan, Hasan Ercan Tutar, Merih Berberoğlu
Publikováno v:
JCRPE, Vol 14, Iss 4, Pp 422-432 (2022)
INTRODUCTION: Cardiac involvement is common in Noonan syndrome (NS). Concerns have been raised regarding the effect of recombinant growth hormone (rGH) use on ventricular wall thickness and a possible increased risk of cardiac side effects. This stud
Externí odkaz:
https://doaj.org/article/39021e7717cf41d081fef725aa761ecd
Publikováno v:
JCRPE, Vol 14, Iss 4, Pp 433-443 (2022)
INTRODUCTION: The harmful or beneficial effect of obesity on bone mineral density (BMD) remains controversial in children and adolescents. Fibroblast growth factor 21 (FGF21) is a metabolic factor that plays a specific role in the regulation of carbo
Externí odkaz:
https://doaj.org/article/d24363aba87745209b820c00473f13dd
Autor:
Aydilek Dağdeviren Çakır, Firdevs Baş, Onur Akın, Zeynep Şıklar, Bahar Özcabı, Merih Berberoğlu, Aslı Derya Kardelen, Elvan Bayramoğlu, Şükran Poyrazoğlu, Murat Aydın, Ayça Törel Ergür, Damla Gökşen, Semih Bolu, Zehra Aycan, Beyhan Tüysüz, Oya Ercan, Olcay Evliyaoğlu
Publikováno v:
JCRPE, Vol 13, Iss 3, Pp 308-319 (2021)
Objective:To investigate clinical characteristics and response to growth hormone (GH) treatment in patients with Prader-Willi syndrome (PWS) in Turkey.Methods:The data of 52 PWS patients from ten centers was retrospectively analyzed. A nation-wide, w
Externí odkaz:
https://doaj.org/article/ce309fa5e23846da9b1e726223897839
Autor:
Şenay Savaş-Erdeve, Zehra Aycan, Semra Çetinkaya, Ayşe Pınar Öztürk, Firdevs Baş, Şükran Poyrazoğlu, Feyza Darendeliler, Elif Özsu, Zeynep Şıklar, Meliha Demiral, Edip Unal, Mehmet Nuri Özbek, Fatih Gürbüz, Bilgin Yüksel, Olcay Evliyaoğlu, Nesibe Akyürek, Merih Berberoğlu
Publikováno v:
JCRPE, Vol 13, Iss 2, Pp 180-186 (2021)
Objective:To retrospectively evaluate the follow-up data in patients with 46,XX congenital adrenal hyperplasia (CAH) who were raised male.Methods:A national database was created. The data of patients were asked to be recorded in the data form.Results
Externí odkaz:
https://doaj.org/article/f9e01545ac464347a539fec859b71f5e