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Pediatric Hematology and Oncology|April 9, 2016
The diagnostic value of soluble urokinase plasminogen activator receptor compared with C-reactive protein and procalcitonin in children with febrile neutropeniaMelis Sirinoglu, Ahmet Soysal, Ayşe Karaaslan, et al.European Journal of Endocrinology|February 4, 2026
Adrenal Androgens as Predictors of Growth Characteristics in Premature PubarcheMehmet Eltan, Zehra Yavas Abali, Aylin Tugba Canbaz, 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.The Journal of Clinical Endocrinology and Metabolism|November 18, 2021
Lack of GNAS Remethylation During Oogenesis May Be a Cause of Sporadic Pseudohypoparathyroidism Type IbAngelo Milioto, Monica Reyes, Patrick Hanna, et al.Journal of Clinical Research in Pediatric Endocrinology|January 26, 2023
Decline in the Age of Menarche in Istanbul Schoolgirls Over the Last 12 YearsTülay Güran, Didem Helvacıoğlu, Büşra Gürpınar Tosun, et al.Calcified Tissue International|April 28, 2020
A Rare Cause of Hypophosphatemia: Raine Syndrome Changing Clinical Features with AgeMehmet Eltan, Ceren Alavanda, Zehra Yavas Abali, et al.European Journal of Endocrinology|March 21, 2019
PPP2R3C gene variants cause syndromic 46,XY gonadal dysgenesis and impaired spermatogenesis in humansTulay Guran, Gozde Yesil, Serap Turan, et al.The Journal of Clinical Endocrinology and Metabolism|December 19, 2024
Clinical and molecular genetic characteristics of patients with hereditary hypophosphatemiaMehmet Eltan, Ceren Alavanda, Zehra Yavas Abali, et al.Hormone Research in Paediatrics|January 11, 2023
Challenges in the Management of a 7-Year-Old Child with Thyrotropin-Secreting Pituitary Adenoma and the Review of the LiteratureTarik Kirkgoz, Saygin Abali, Askin Seker, et al.The Journal of Clinical Endocrinology and Metabolism|September 17, 2009
Hypogonadotropic hypogonadism due to a novel missense mutation in the first extracellular loop of the neurokinin B receptorTulay Guran, Gwen Tolhurst, Abdullah Bereket, et al.Pageof 16