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Semra Çeti̇nkaya

dr. sami ulus training and research hospital

25H指数
299论文数
2.3K被引数
收录论文 29
发表时间
Early dextrose and lower-chloride fluids in pediatric diabetic ketoacidosis: a faster and safer approach? - A multicenter cohort study早期葡萄糖和低氯液体在儿童糖尿病酮症酸中毒中的应用:更快且更安全的方法?——一项多中心队列研究
err2026-09-24
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errOAAI
errGürkan Tarçın; Emre Özer; Gülin Karacan Küçükali; Ayşe Yaşar; Aydilek Dağdeviren Çakır; Hasan Karakaş; Serhat Emeksiz; Can Demir Karacan; Ahmet Uçar; Heves Kırmızıbekmez; Semra Çetinkaya; Mehmet Boyraz; Sinem Oral Cebeci; Hande Turan; Elvan Bayramoğlu; Fatih Aygün; Olcay Evliyaoğlu
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Genotype–Phenotype Spectrum of Non-Syndromic Monogenic Obesity in a National Paediatric Cohort非综合征性单基因肥胖在一个国家儿科队列中的基因型-表型谱
err2026-05-28
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errOAAI
errAhmet Kahveci; Selin Uzun Karauzum; Hayrullah Manyas; Behiye Sarikaya Ozdemir; Zerrin Orbak; Ummahan Tercan; Ruken Yildirim; Nihal Hatipoglu; Fatih Kilci; Hatice Nursoy; Servan Ozalkak; Baris Kolbasi; Semra Cetinkaya; Hazal Canbaz Ozdemir; Mesut Parlak; Filiz Tutunculer Kokenli; Emine Camtosun; Saime Ergen Dibeklioglu; Gonul Buyukyilmaz; Ayse Derya Bulus; Hanife Gul Balki; Ayse Ozden; E. Nazli Gonc; Elif Ozsu; Huseyin Demirbilek; Melek Yildiz; Samim Ozen; Abdullah Bereket; Belma Haliloglu
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Neonatal diabetes mellitus is a significant feature of COXPD-24 caused by recessive NARS2 variants新生儿糖尿病是因隐性NARS2变异引起的COXPD-24的一个显著特征。
err2025-08-31
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errOAAI
errRussell Donis; Matthew N. Wakeling; Nicola Jeffery; Molly Govier; Matthew B. Johnson; Samar Sabir Hassan; Mohammed Ahmed Abdullah; Khadiga Yehia Elsayed Eltonbary; Nima Parvaneh; Mahsa M. Amoli; Farzaneh Abbasi; Selin Elmaoğulları; Semra Çetinkaya; Kubra Gunes; Meltem Tayfun; Hanieh Yaghootkar; Andrew T. Hattersley; Sarah E. Flanagan; Elisa De Franco
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Central precocious puberty in boys; diagnosis, treatment and follow-up: a nation-wide study男孩中枢性性早熟:诊断、治疗及随访——一项全国性研究
err2025-08-11
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PREAI
errSevinc Odabasi Gunes; Merve Sakar; Nursel Muratoglu Sahin; Gulay Karaguzel; Emine Ayca Cimbek; Feyza Darendeliler; Ezgi Sarban; Esra Doger; Ganimet Oner; Zeynep Siklar; Gizem Senyazar; Murat Aydin; Behzat Ozkan; Ozlem Sangun; Mesut Parlak; Onur Akin; Kadriye Cansu Sahin; İhsan Esen; Aylin Kilinc Ugurlu; Gulcan Seymen; Semih Bolu; Elif Sobu; Servan Ozalkak; Emine Demet Akbas; Gonul Buyukyilmaz; Beray Selver Eklioglu; Ahmet Ucar; Pinar Kocaay; Selma Tunc; Serpil Bas; İsmail Dundar; Eda Celebi Bitkin; Ayca Torel Ergur; Dilek Bingol Aydin; Birgul Kirel; Aysun Ata; Muge Atar; Mehmet Isakoca; Emel Hatun Aytac Kaplan; Tugba Kontbay; Derya Tepe; Oya Ercan; Mehmet Boyraz; Nesibe Akyurek; Edip Unal; Nurhan Ozcan Murat; Serkan Bilge Koca; Zumrut Kocabey Sutcu; Feyza Nehir Oznur Muz; Semra Cetinkaya
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17α Hydroxylase/17,20 lyase deficiency: clinical features and genetic insights from a large Turkey cohort
err2024-07-17
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errSiklar, Zeynep; Camtosun, Emine; Bolu, Semih; Yildiz, Melek; Akinci, Aysehan; Bas, Firdevs; Dundar, Ismail; Bestas, Asli; Unal, Edip; Kocaay, Pinar; Guran, Tulay; Buyukyilmaz, Gonul; Ugurlu, Aylin Kilinc; Tosun, Busra Gurpinar; Turan, Ihsan; Kurnaz, Erdal; Yuksel, Bilgin; Turkkahraman, Doga; Cayir, Atilla; Celmeli, Gamze; Gonc, E. Nazli; Eklioglu, Beray Selver; Cetinkaya, Semra; Yilmaz, Seniha Kiremitci; Atabek, Mehmet Emre; Buyukinan, Muammer; Arslan, Emrullah; Mengen, Eda; Cakir, Esra Deniz Papatya; Karaoglan, Murat; Hatipoglu, Nihal; Orbak, Zerrin; Ucar, Ahmet; Akyurek, Nesibe; Akbas, Emine Demet; Isik, Emregul; Kaygusuz, Sare Betul; Sutcu, Zumrut Kocabey; Seymen, Gulcan; Berberoglu, Merih
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High frequency of transient congenital hypothyroidism among infants referred for suspected congenital hypothyroidism from the Turkish National screening program: thyroxine dose may guide the prediction of transients
err2024-03-28
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errOzer, Y.; Anik, A.; Sayili, U.; Tercan, U.; Sevim, R. Deveci; Gunes, S.; Pirimoglu, M. Buhur; Elmaogullari, S.; Dundar, I.; Okdemir, D.; Besci, O.; Jalilova, A.; Cicek, D.; Singin, B.; Ulu, S. E.; Turan, H.; Albayrak, S.; Sutcu, Z. Kocabey; Eklioglu, B. S.; Eren, E.; Cetinkaya, S.; Savas-Erdeve, S.; Esen, I.; Demir, K.; Darcan, S.; Hatipoglu, N.; Parlak, M.; Dursun, F.; Siklar, Z.; Berberoglu, M.; Keskin, M.; Orbak, Z.; Tezel, B.; Yuruker, E.; Keskinkilic, B.; Kara, F.; Erginoz, E.; Darendeliler, F.; Evliyaoglu, O.
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Decreased calcium permeability caused by biallelic TRPV5 mutation leads to autosomal recessive renal calcium-wasting hypercalciuria
err2024-03-25
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errLafci, Naz Guleray; van Goor, Mark; Cetinkaya, Semra; van der Wijst, Jenny; Acun, Melisa; Colak, Fatma Kurt; Cetinkaya, Arda; Hoenderop, Joost
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Clinical features, diagnosis and treatment outcomes of Cushing's disease in children: A multicenter study
err2023-10-10
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PREAI
errTarcin, Gurkan; Catli, Gonul; Cetinkaya, Semra; Eren, Erdal; Kardelen, Asli Derya; Akinci, Aysehan; Bober, Ece; Kara, Cengiz; Yildirim, Ruken; Er, Eren; Polat, Recep; Ozhan, Bayram; Yildiz, Melek; Kor, Yilmaz; Evliyaoglu, Olcay; Dundar, Bumin; Ercan, Oya
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Evaluation of aggression level in adolescent girls with classical congenital adrenal hyperplasia
err2023-06-26
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errOAAI
errIsik, Recep Oguzhan; Kizilcan Cetin, Sirmen; Cetinkaya, Semra; Berberoglu, Merih; Siklar, Zeynep; Ozsu, Elif; Aycan, Zehra
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A National Multicenter Study of Leptin and Leptin Receptor Deficiency and Systematic Review
err2023-02-24
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PREAI
errBesci, Ozge; Firat, Sevde Nur; Ozen, Samim; Cetinkaya, Semra; Akin, Leyla; Kor, Yilmaz; Pekkolay, Zafer; Ozalkak, Servan; Ozsu, Elif; Erdeve, Senay Savas; Poyrazoglu, Suekran; Berberoglu, Merih; Aydin, Murat; Omma, Tulay; Akinci, Baris; Demir, Korcan; Oral, Elif Arioglu
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PLXNB1 mutations in the etiology of idiopathic hypogonadotropic hypogonadism特发性低促性腺激素性性腺功能减退症的病因中的PLXNB1突变
err2022-02-16
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PREAI
errWelch, Bradley A.; Cho, Hyun-Ju; Ucakturk, Seyit Ahmet; Farmer, Stephen Matthew; Cetinkaya, Semra; Abaci, Ayhan; Akkus, Gamze; Simsek, Enver; Kotan, Leman Damla; Turan, Ihsan; Gurbuz, Fatih; Yuksel, Bilgin; Wray, Susan; Topaloglu, A. Kemal
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Insights From Long-term Follow-up of a Girl With Adrenal Insufficiency and Sphingosine-1-Phosphate Lyase Deficiency
err2022-02-11
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errMaharaj, Avinaash; Guran, Tulay; Buonocore, Federica; Achermann, John C.; Metherell, Louise; Prasad, Rathi; Cetinkaya, Semra
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Functional assessment of variants associated with Wolfram syndrome
err2019-10-10
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errRiachi, Melissa; Yilmaz, Sebahat; Kurnaz, Erdal; Aycan, Zehra; Cetinkaya, Semra; Tranebjaerg, Lisbeth; Rendtorff, Nanna Dahl; Bitner-Glindzicz, Maria; Bockenhauer, Detlef; Hussain, Khalid
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Renal complications of lipodystrophy: A closer look at the natural history of kidney disease脂肪营养不良的肾脏并发症: 仔细观察肾脏疾病的自然史
err2018-05-17
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errAkinci, Baris; Unlu, Sadiye Mehtat; Celik, Ali; Simsir, Ilgin Yildirim; Sen, Sait; Nur, Banu; Keskin, Fatma Ela; Saydam, Basak Ozgen; Ozdemir, Nilufer Kutbay; Yurekli, Banu Sarer; Ergur, Bekir Ugur; Sonmez, Melda; Atik, Tahir; Arslan, Atakan; Demir, Tevfik; Altay, Canan; Tunc, Ulku Aybuke; Arkan, Tugba; Gen, Ramazan; Eren, Erdal; Akinci, Gulcin; Yilmaz, Aslihan Arasli; Bilen, Habib; Ozen, Samim; Celtik, Aygul; Erdeve, Senay Savas; Cetinkaya, Semra; Onay, Huseyin; Sarioglu, Sulen; Oral, Elif Arioglu
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Clinical and genetic characterisation of a series of patients with triple A syndrome
err2017-12-19
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PREAI
errKurnaz, Erdal; Duminuco, Paolo; Aycan, Zehra; Savas-Erdeve, Senay; Sahin, Nursel Muratoglu; Keskin, Melisah; Bayramoglu, Elvan; Bonomi, Marco; Cetinkaya, Semra
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