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Endocrine Practice : Official Journal of the American College of Endocrinology and the American Association of Clinical Endocrinologists|September 10, 2013
Adherence to growth hormone therapy: results of a multicenter studyBanu Küçükemre Aydın, Zehra Aycan, Zeynep Sıklar, et al.Journal of Clinical Research in Pediatric Endocrinology|December 30, 2020
Clinical Characteristics of 46,XX Males with Congenital Adrenal HyperplasiaŞenay Savaş-Erdeve, Zehra Aycan, Semra Çetinkaya, et al.Sexual Development : Genetics, Molecular Biology, Evolution, Endocrinology, Embryology, and Pathology of Sex Determination and Differentiation|March 14, 2023
Pubertal and Gonadal Outcomes in 46,XY Individuals with Partial Androgen Insensitivity Syndrome Raised as GirlsGuilherme Guaragna-Filho, Gil Guerra-Junior, Rieko Tadokoro-Cuccaro, et al.Journal of Clinical Research in Pediatric Endocrinology|March 12, 2020
Neonatal Screening for Congenital Adrenal Hyperplasia in Turkey: Outcomes of Extended Pilot Study in 241,083 InfantsTülay Güran, Başak Tezel, Meltem Çakır, et al.Journal of Clinical Research in Pediatric Endocrinology|March 15, 2024
Adherence to Growth Hormone Treatment in Children During the COVID-19 PandemicErdal Eren, Semra Çetinkaya, Yasemin Denkboy Öngen, et al.Clinical Endocrinology|December 15, 2012
Thyroid dyshormonogenesis is mainly caused by TPO mutations in consanguineous communityHakan Cangul, Zehra Aycan, Alvaro Olivera-Nappa, et al.The Journal of Clinical Endocrinology and Metabolism|March 31, 2017
Birth Weight in Different Etiologies of Disorders of Sex DevelopmentSukran Poyrazoglu, Feyza Darendeliler, S Faisal Ahmed, et al.Endocrine|December 16, 2014
Molecular analysis of PROP1, POU1F1, LHX3, and HESX1 in Turkish patients with combined pituitary hormone deficiency: a multicenter studyFirdevs Baş, Z Oya Uyguner, Feyza Darendeliler, et al.Therapeutic Advances in Endocrinology and Metabolism|August 20, 2025
A database study of the safety and effectiveness of daily growth hormone in treating more than 80,000 children with growth disorders worldwide: a plain language summary of publicationMohamad Maghnie, Michael B Ranke, Mitchell E Geffner, et al.Genetics in Medicine : Official Journal of the American College of Medical Genetics|January 26, 2021
Loss-of-function variants in SEMA3F and PLXNA3 encoding semaphorin-3F and its receptor plexin-A3 respectively cause idiopathic hypogonadotropic hypogonadismLeman Damla Kotan, Gaetan Ternier, Aydilek Dagdeviren Cakir, et al.Pageof 22