Showing results (1-10 of 9) with videos related to
Sort By:
Pageof 1
Talanta|October 11, 2015
Polymer/carbon nanotubes coated graphite surfaces for highly sensitive nitrite detectionFiliz Kuralay, Mehmet Dumangöz, Selma TunçTalanta|September 4, 2016
Biosensing applications of titanium dioxide coated graphene modified disposable electrodesFiliz Kuralay, Selma Tunç, Ferhat Bozduman, et al.Journal of Clinical Research in Pediatric Endocrinology|January 4, 2017
Higher-Than-Conventional Subcutaneous Regular Insulin Doses Following Diabetic Ketoacidosis in Children and AdolescentsÖzlem Bağ, Selma Tunç, Özlem Nalbantoğlu, et al.Turkish Journal of Medical Sciences|March 14, 2019
Long-term monitoring of Graves’ disease in children and adolescents: a single-center
experienceSelma Tunç, Özge Köprülü, Hatice Ortaç, et al.Journal of Pediatric Endocrinology & Metabolism : JPEM|July 17, 2015
A novel mutation of AMH in three siblings with persistent Mullerian duct syndromeÖzlem Nalbantoğlu, Korcan Demir, Hüseyin Anıl Korkmaz, et al.Journal of Clinical Research in Pediatric Endocrinology|January 11, 2022
Revisiting the Annual Incidence of Type 1 Diabetes Mellitus in Children from the Southeastern Anatolian Region of Turkey: A Regional ReportŞervan Özalkak, Ruken Yıldırım, Selma Tunç, et al.Journal of Clinical Research in Pediatric Endocrinology|February 21, 2017
Melanocortin-4 Receptor Gene Mutations in a Group of Turkish Obese Children and AdolescentsSelma Tunç, Korcan Demir, Fatma Ajlan Tükün, et al.Journal of Pediatric Endocrinology & Metabolism : JPEM|April 17, 2015
Two different patterns of mini-puberty in two 46,XY newborns with 17β-hydroxysteroid dehydrogenase type 3 deficiencyKorcan Demir, Melek Yıldız, Özlem Nalbantoğlu Elmas, et al.Archivos Argentinos De Pediatria|May 16, 2017
Infantile-onset thiamine responsive megaloblastic anemia syndrome with SLC19A2 mutation: a case reportNagehan Katipoğlu, Tuba H Karapinar, Korean Demir, et al.Pageof 1