日期:
2020 年 — 2026 年
2020
2021
2022
2023
2024
2025
2026
影响因子:

Multidisciplinary Tumor Board Evaluation of Pediatric Patients with Adrenocortical Tumors Across Seven International Centers

七个国际中心对患有肾上腺皮质肿瘤的儿科患者进行多学科肿瘤委员会评估

Riedmeier, Maria; Schlötelburg, Wiebke; Agarwal, Shipra; Biswas, Ahitagni; Ekinci, Saniye; Fassnacht, Martin; Villares Fragoso, Maria C B; Gonc, E Nazli; Gultekin, Melis; Haliloglu, Mithat; Jain, Vishesh; Jana, Manisha; Janus, Dominika; Meena, Jagdish Prasad; Munarin, Jessica; Orhan, Diclehan; Del Rivero, Jaydira; Sharma, Rajni; Tuli, Gerdi; Yalcin, Bilgehan; Wiegering, Verena

CYB5R4 Gene Methylation as a Potential Epigenetic Marker for Ovarian Cancer.

CYB5R4基因甲基化作为卵巢癌的潜在表观遗传标记

Gonc Aysegul, Sukruoglu Erdogan Ozge, Kilic Erciyas Seda, Celik Demirbas Betul, Dinc Ahmet, Pasin Ozge, Saip Pınar, Yazici Hulya, Tuncer Seref Bugra

COVID-19 Detection From Respiratory Sounds With Hierarchical Spectrogram Transformers

利用分层频谱图变换器从呼吸音中检测 COVID-19

Aytekin, Idil; Dalmaz, Onat; Gonc, Kaan; Ankishan, Haydar; Saritas, Emine Ulku; Bagci, Ulas; Celik, Haydar; Cukur, Tolga

Epidemiology of type 1 diabetes mellitus in children and adolescents: A 50-year, single-center experience

儿童和青少年1型糖尿病的流行病学:一项为期50年的单中心经验

Kandemir, Nurgun; Vuralli, Dogus; Ozon, Alev; Gonc, Nazlı; Ardicli, Didem; Jalilova, Lala; Gulcek, Omer Nazim; Alikasifoglu, Ayfer

17α Hydroxylase/17,20 lyase deficiency: clinical features and genetic insights from a large Turkey cohort

17α羟化酶/17,20裂解酶缺乏症:来自土耳其大型队列的临床特征和遗传学见解

Siklar, Zeynep; Camtosun, Emine; Bolu, Semih; Yildiz, Melek; Akinci, Aysehan; Bas, Firdevs; Dündar, İsmail; Bestas, Asli; Ünal, Edip; Kocaay, Pinar; Guran, Tulay; Buyukyilmaz, Gonul; Ugurlu, Aylin Kilinc; Tosun, Buşra Gurpinar; Turan, Ihsan; Kurnaz, Erdal; Yuksel, Bilgin; Turkkahraman, Doga; Cayir, Atilla; Celmeli, Gamze; Gonc, E Nazli; Eklioğlu, 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, Emregül; Kaygusuz, Sare Betul; Sutcu, Zumrut Kocabey; Seymen, Gulcan; Berberoglu, Merih

Dual-basal-insulin regimen for the management of dawn phenomenon in children with type 1 diabetes: a retrospective cohort study

双基础胰岛素方案治疗1型糖尿病儿童黎明现象:一项回顾性队列研究

Celik, Nur Berna; Canoruc Emet, Dicle; Canturk, Merve; Ozon, Z Alev; Gonc, E Nazli

Case Report: Severe McCune-Albright syndrome presenting with neonatal Cushing syndrome: navigating through clinical obstacles

病例报告:重症 McCune-Albright 综合征合并新生儿库欣综合征:克服临床障碍

Unsal, Yagmur; Gozmen, Onur; User, İdil Rana; Hızarcıoglu, Hayriye; Gulhan, Bora; Ekinci, Saniye; Karagoz, Tevfik; Ozon, Z Alev; Gonc, E Nazlı

Early weight gain after diagnosis may have an impact on remission status in children with new-onset type 1 diabetes mellitus

确诊后早期体重增加可能会影响新发1型糖尿病儿童的缓解状态。

Emet, Dicle Canoruc; Karavar, Hande Nur; Gozmen, Onur; Agyar, Arife Aslan; Ünsal, Yağmur; Canturk, Merve; Cengiz, Pınar; Vuralli, Dogus; Ozon, Z Alev; Gonc, E Nazlı

PROPROTEIN CONVERTASE 1/3 DEFICIENCY WITH PELVIC EWING SARCOMA

原蛋白转化酶 1/3 缺乏症伴盆腔尤文氏肉瘤

Oral, H; Guven, D C; Özdemir, D Ateş; Usubütün, A; Gonc, N; Arik, Z

Combined pituitary hormone deficiency due to gross deletions in the POU1F1 (PIT-1) and PROP1 genes

由于 POU1F1 (PIT-1) 和 PROP1 基因的大片段缺失导致的垂体激素联合缺乏症

Bertko, Eleonore; Klammt, Jürgen; Dusatkova, Petra; Bahceci, Mithat; Gonc, Nazli; Ten Have, Louise; Kandemir, Nurgun; Mansmann, Georg; Obermannova, Barbora; Oostdijk, Wilma; Pfäffle, Heike; Rockstroh-Lippold, Denise; Schlicke, Marina; Tuzcu, Alpaslan Kemal; Pfäffle, Roland