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Journal of Clinical Research in Pediatric Endocrinology|April 24, 2026
BMI-SDS Changes During GnRHa Therapy in 150 Girls with Idiopathic Central Precocious Puberty: Follow-up Through Final HeightDidem Helvacıoğlu, Busra Gurpinar Tosun, Sefa Öğe, et al.American Journal of Medical Genetics. Part A|March 22, 2019
Ptosis as a unique hallmark for autosomal recessive WNT1-associated osteogenesis imperfectaSheela Nampoothiri, Brecht Guillemyn, Nursel Elcioglu, et al.European Journal of Endocrinology|October 19, 2011
Pitfalls in the diagnosis of thyroid dysgenesis by thyroid ultrasonography and scintigraphyElif Karakoc-Aydiner, Serap Turan, Ihsan Akpinar, et al.The Journal of Clinical Endocrinology and Metabolism|February 17, 2012
An atypical case of familial glucocorticoid deficiency without pigmentation caused by coexistent homozygous mutations in MC2R (T152K) and MC1R (R160W)Serap Turan, Claire Hughes, Zeynep Atay, et al.Journal of Pediatric Endocrinology & Metabolism : JPEM|January 3, 2025
Thyroid surgery in pediatric age: a 10-year experience at a single center and literature reviewOrhan Asya, Ali Cemal Yumusakhuylu, Yavuz Gundogdu, et al.Bone|February 1, 2022
A novel deletion involving the first GNAS exon encoding Gsα causes PHP1A without methylation changes at exon A/BDevon Campbell, Monica Reyes, Sare Betul Kaygusuz, et al.Hormone Research in Paediatrics|November 4, 2020
Cinacalcet as a First-Line Treatment in Neonatal Severe Hyperparathyroidism Secondary to Calcium Sensing Receptor (CaSR) MutationSinem Gulcan-Kersin, Tarik Kirkgoz, Mehmet Eltan, et al.Journal of Clinical Research in Pediatric Endocrinology|January 29, 2011
Circulating insulin-like growth factor binding protein-4 (IGFBP-4) is not regulated by parathyroid hormone and vitamin D in vivo: evidence from children with ricketsAbdullah Bereket, Yaşar Cesur, Behzat Özkan, et al.Pediatric Research|September 24, 2021
Adrenal steroids reference ranges in infancy determined by LC-MS/MSEce Oge Enver, Pinar Vatansever, Omer Guran, et al.Hormone Research in Paediatrics|March 29, 2021
Genotypic Sex and Severity of the Disease Determine the Time of Clinical Presentation in Steroid 17α-Hydroxylase/17,20-Lyase DeficiencyErdal Kurnaz, Emine Kartal Baykan, Ayberk Türkyılmaz, et al.Pageof 16