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

The Results of 16 Years of Iodization: Assessment of Iodine Deficiency Among School-age Children in Antalya, Turkey

土耳其安塔利亚学龄儿童碘缺乏症评估：16 年碘化政策实施成果

期刊:Journal of Clinical Research in Pediatric Endocrinology
影响因子:1.5
doi:10.4274/jcrpe.galenos.2020.2019.0168
Çelmeli, Gamze; Çürek, Yusuf; Özen Küçükçetin, İkbal; Arslan Gülten, Zümrüt; Özdem, Sebahat; Akçurin, Sema; Bircan, İffet
发表日期：2020
文献求助 收藏

Remarkable Increase in the Prevalence of Overweight and Obesity Among School Age Children in Antalya, Turkey, Between 2003 and 2015

2003年至2015年间，土耳其安塔利亚学龄儿童超重和肥胖患病率显著增加

期刊:Journal of Clinical Research in Pediatric Endocrinology
影响因子:1.5
doi:10.4274/jcrpe.galenos.2018.2018.0108
Çelmeli, Gamze; Çürek, Yusuf; Arslan Gülten, Zümrüt; Yardımsever, Mehmet; Koyun, Mustafa; Akçurin, Sema; Bircan, İffet
肥胖
代谢
发表日期：2019
文献求助 收藏

Comparison of Sharp Dissection, Electrocautery, and Ultrasonic Activated Scalpel with Regard to Endothelial Damage, Preparation Time, and Postoperative Bleeding During Radial Artery Harvesting

锐器分离、电灼和超声刀在桡动脉取材过程中对内皮损伤、准备时间和术后出血的比较

期刊:Revista Brasileira De Cirurgia Cardiovascular
影响因子:1.1
doi:10.21470/1678-9741-2018-0311
Dinçer Uysal, Şenol Gülmen, Hayrettin Özkan, Ulaş Sağlam, Mustafa Etli, Sema Bircan, Recep Sütçü, Turhan Yavuz, Hakan Öntaş, Fatih Aksoy
信号转导
ICAM1
发表日期：2019
文献求助 收藏

Clinical and Molecular Genetic Analysis in Three Children with Wolfram Syndrome: A Novel WFS1 Mutation (c.2534T>A)

三名沃尔夫拉姆综合征患儿的临床和分子遗传学分析：一种新的WFS1突变（c.2534T>A）

期刊:Journal of Clinical Research in Pediatric Endocrinology
影响因子:1.5
doi:10.4274/jcrpe.2894
Çelmeli, Gamze; Türkkahraman, Doğa; Çürek, Yusuf; Houghton, Jayne; Akçurin, Sema; Bircan, İffet
发表日期：2017
文献求助 收藏

A combination of nifedipine and octreotide treatment in an hyperinsulinemic hypoglycemic infant

硝苯地平和奥曲肽联合治疗高胰岛素血症低血糖婴儿

期刊:Journal of Clinical Research in Pediatric Endocrinology
影响因子:1.5
doi:10.4274/Jcrpe.1230
Durmaz, Erdem; Flanagan, Sarah E; Parlak, Mesut; Ellard, Sian; Akcurin, Sema; Bircan, Iffet
免疫/内分泌
发表日期：2014
文献求助 收藏

Wolcott-Rallison syndrome due to a novel mutation (R491X) in EIF2AK3 gene

沃尔科特-拉利森综合征是由EIF2AK3基因中的一种新突变（R491X）引起的

期刊:Journal of Clinical Research in Pediatric Endocrinology
影响因子:1.5
doi:10.4274/jcrpe.619
Mihci, Ercan; Türkkahraman, Doğa; Ellard, Sian; Akçurin, Sema; Bircan, Iffet
EIF2A
发表日期：2012
文献求助 收藏