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Sexual Development : Genetics, Molecular Biology, Evolution, Endocrinology, Embryology, and Pathology of Sex Determination and Differentiation|January 6, 2026
Molecular Diagnosis of 46,XY Disorders of Sex Development: An Efficient Initial Molecular Analysis Using a Custom-Designed Targeted Gene Panel in a Single-Center StudySukran Poyrazoglu, Agharza Aghayev, Guven Toksoy, et al.The Journal of Clinical Endocrinology and Metabolism|December 5, 2025
Impact of Growth-promoting Therapies on Puberty, Growth, and Final Height in Classical 21-hydroxylase DeficiencyZehra Yavas Abali, Melek Yildiz, Saygin Abali, et al.Hormone Research in Paediatrics|July 18, 2023
A Novel RNPC3 Gene Variant Expands the Phenotype in Patients with Congenital Hypopituitarism and NeuropathyZehra Yavas Abali, Ezgi Gokpinar Ili, Firdevs Bas, et al.Endocrine|May 18, 2025
Comprehensive clinical and molecular characterization with long-term outcomes in 40 patients with congenital hyperinsulinismZehra Yavas Abali, Firdevs Bas, Jayne A L Houghton, et al.European Journal of Pediatrics|December 2, 2008
The role of leptin, soluble leptin receptor, resistin, and insulin secretory dynamics in the pathogenesis of hypothalamic obesity in childrenTulay Guran, Serap Turan, Abdullah Bereket, et al.Journal of Pediatric and Adolescent Gynecology|February 8, 2017
Evaluation and Treatment Results of Ovarian Cysts in Childhood and Adolescence: A Multicenter, Retrospective Study of 100 PatientsBanu Kucukemre Aydin, Nurcin Saka, Firdevs Bas, et al.Journal of Pediatric Endocrinology & Metabolism : JPEM|October 2, 2008
Evaluation of diagnosis and treatment results in children with Graves' disease with emphasis on the pubertal status of patientsSükran Poyrazoğlu, Nurcin Saka, Firdevs Bas, et al.American Journal of Human Genetics|January 1, 2013
Next-generation sequencing reveals deep intronic cryptic ABCC8 and HADH splicing founder mutations causing hyperinsulinism by pseudoexon activationSarah E Flanagan, Weijia Xie, Richard Caswell, et al.European Journal of Endocrinology|October 29, 2021
Broad-spectrum XX and XY gonadal dysgenesis in patients with a homozygous L193S variant in PPP2R3CDilek Cicek, Nick Warr, Gozde Yesil, et al.The Journal of Clinical Endocrinology and Metabolism|April 8, 2021
Clinical and Hormonal Profiles Correlate With Molecular Characteristics in Patients With 11β-Hydroxylase DeficiencyMelek Yildiz, Emregul Isik, Zehra Yavas Abali, et al.Pageof 8