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Journal of Clinical Research in Pediatric Endocrinology|March 27, 2020
Gender Identity and Assignment Recommendations in Disorders of Sex Development Patients: 20 Years’ Experience and ChallengesFatih Gürbüz, Murat Alkan, Gonca Çelik, et al.
The Turkish Journal of Pediatrics|April 7, 2018
Impaired glucose tolerance in Fanconi-Bickel syndrome: Eight patients with two novel mutationsBerna Şeker-Yılmaz, Deniz Kör, Fatma Derya Bulut, et al.
Journal of Clinical Research in Pediatric Endocrinology|February 15, 2011
Evaluation of permanent growth hormone deficiency (GHD) in young adults with childhood onset GHD: a multicenter studyMerih Berberoğlu, Zeynep Sıklar, Feyza Darendeliler, et al.
Frontiers in Pediatrics|August 18, 2025
Depression, anxiety in adolescents with exogenous obesity and depression, anxiety, caregiver burden, and burnout in their mothersCan Celiloğlu, İhsan Turan, Perihan Çam Ray, et al.
Journal of Clinical Research in Pediatric Endocrinology|December 24, 2016
Hypogonadotropic Hypogonadism due to Novel FGFR1 MutationsGamze Akkuş, Leman Damla Kotan, Erdem Durmaz, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|December 16, 2003
Idiopathic hyperphosphatasia and TNFRSF11B mutations: relationships between phenotype and genotypeBelinda Chong, Madhuri Hegde, Matthew Fawkner, et al.
Hormone Research in Paediatrics|August 8, 2013
The novel mutation p.Trp147Arg of the steroidogenic acute regulatory protein causes classic lipoid congenital adrenal hyperplasia with adrenal insufficiency and 46,XY disorder of sex developmentBilgin Yüksel, Alexandra E Kulle, Fatih Gürbüz, et al.
The Journal of Clinical Endocrinology and Metabolism|January 19, 2010
Congenital lipoid adrenal hyperplasia: functional characterization of three novel mutations in the STAR geneSusanne Bens, Angelika Mohn, Bilgin Yüksel, et al.
The Turkish Journal of Pediatrics|March 10, 2017
Genotypic and phenotypic features of the cystinosis patients from the South Eastern part of TurkeyNeslihan Önenli-Mungan, Deniz Kör, Aysun Karabay-Bayazıt, et al.
Calcified Tissue International|January 16, 2026
Targeting Hypercalciuria in SLC34A1-Related Disorders: Impact of Oral Phosphate Therapy and Novel Genetic Insights in Pediatric Case SeriesIhsan Turan, Muge Atar, Mehmet Eltan, et al.
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