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Journal of Clinical Research in Pediatric Endocrinology|February 9, 2022
Mutations in AR or SRD5A2 Genes: Clinical Findings, Endocrine Pitfalls, and Genetic Features of Children with 46,XY DSDNeşe Akcan, Oya Uyguner, Firdevs Baş, et al.Hormone Research in Paediatrics|May 20, 2025
Exploring the Heterogeneity of Pediatric Neuroendocrine Tumors: Single-Center ExperienceCansu Koc, Yaprak Ece Yola Atalah, Sedat Bayrakoglu, et al.Journal of Clinical Research in Pediatric Endocrinology|October 10, 2024
Gonadoblastoma with Dysgerminoma in a Virilized Adolescent with Karyotype 46,XX: A Case Report and Review of the LiteratureTuğçe Kandemir, Esin Karakilic Ozturan, Özlem Dural, et al.The Journal of Steroid Biochemistry and Molecular Biology|April 8, 2018
Prevalence, clinical characteristics and long-term outcomes of classical 11 β-hydroxylase deficiency (11BOHD) in Turkish population and novel mutations in CYP11B1 geneFirdevs Baş, Güven Toksoy, Berrin Ergun-Longmire, et al.Omics : a Journal of Integrative Biology|June 26, 2021
Monogenic Childhood Diabetes: Dissecting Clinical Heterogeneity by Next-Generation Sequencing in Maturity-Onset Diabetes of the YoungDeniz Kanca Demirci, Feyza Darendeliler, Sukran Poyrazoglu, et al.Journal of Clinical Research in Pediatric Endocrinology|July 14, 2011
Serum IGF-1 and IGFBP-3 levels in healthy children between 0 and 6 years of ageBilgin Yüksel, M Nuri Özbek, Neslihan Önenli Mungan, et al.American Journal of Medical Genetics. Part A|April 8, 2022
Evaluation of growth, puberty, osteoporosis, and the response to long-term bisphosphonate therapy in four patients with osteoporosis-pseudoglioma syndromeEsin Karakilic-Ozturan, Umut Altunoglu, Ayse Pinar Ozturk, et al.Pediatric Cardiology|February 3, 2018
Determinants of Increased Aortic Diameters in Young Normotensive Patients With Turner Syndrome Without Structural Heart DiseaseA Uçar, Melike Tuğrul, Bülent Oğuz Erol, et al.Journal of Clinical Research in Pediatric Endocrinology|September 17, 2025
Type 1 Diabetes Mellitus and Transfer from Pediatric to Adult Care: A Single-Center ExperienceBetül Yiğit Yalçın, Ummahan Tercan, Melek Yildiz, et al.Journal of Clinical Research in Pediatric Endocrinology|March 30, 2018
A Rare Cause of Congenital Adrenal Hyperplasia: Clinical and Genetic Findings and Follow-up Characteristics of Six Patients with 17-Hydroxylase Deficiency Including Two Novel MutationsAslı Derya Kardelen, Güven Toksoy, Firdevs Baş, et al.Pageof 20