| Primary adrenal insufficiency in children: Diagnosis and management T Kirkgoz, T Guran Best Practice & Research Clinical Endocrinology & Metabolism 32 (4), 397-424, 2018 | 71 | 2018 |
| Does COVID-19 predispose patients to type 1 diabetes mellitus? A Ata, A Jalilova, T Kırkgöz, H Işıklar, G Demir, YA Altınok, B Özkan, ... Clinical Pediatric Endocrinology 31 (1), 33-37, 2022 | 25 | 2022 |
| Does genotype–phenotype correlation exist in vitamin D-dependent Rickets type IA: report of 13 new cases and review of the literature SB Kaygusuz, C Alavanda, T Kirkgoz, M Eltan, Z Yavas Abali, ... Calcified Tissue International 108, 576-586, 2021 | 22 | 2021 |
| Cinacalcet as a First-Line Treatment in Neonatal Severe Hyperparathyroidism Secondary to Calcium Sensing Receptor (CaSR) Mutation S Gulcan-Kersin, T Kirkgoz, M Eltan, T Rzayev, P Ata, H Bilgen, E Ozek, ... Hormone research in paediatrics 93 (5), 313-321, 2021 | 16 | 2021 |
| A rare cause of hypophosphatemia: Raine syndrome changing clinical features with age M Eltan, C Alavanda, Z Yavas Abali, P Ergenekon, N Yalındag Ozturk, ... Calcified Tissue International 107, 96-103, 2020 | 12 | 2020 |
| Management of systemic hypersensitivity reactions to gonadotropin-releasing hormone analogues during treatment of central precocious puberty T Kirkgoz, E Karakoc-Aydiner, F Bugrul, Z Yavas Abali, D Helvacioglu, ... Hormone Research in Paediatrics 93 (1), 66-72, 2020 | 9 | 2020 |
| Persistent Müllerian duct syndrome: a rare but important etiology of inguinal hernia and cryptorchidism F Bugrul, ZY Abali, T Kirkgoz, KK Cerit, A Canmemis, S Turan, H Tugtepe, ... Sexual Development 13 (5-6), 264-270, 2020 | 6 | 2020 |
| Low DHEAS concentration in a girl presenting with short stature and premature pubarche: a novel PAPSS2 gene mutation M Eltan, Z Yavas Abali, E Arslan Ates, T Kirkgoz, SB Kaygusuz, ... Hormone Research in Paediatrics 92 (4), 262-268, 2020 | 6 | 2020 |
| Evaluation of growth and puberty in a child with a novel TBX19 gene mutation and review of the literature ZY Abali, G Yesil, T Kirkgoz, SB Kaygusuz, M Eltan, S Turan, A Bereket, ... Hormones 18, 229-236, 2019 | 6 | 2019 |
| Comparison of axillary and tympanic temperature measurements in children diagnosed with acute otitis media HH Doğan, RG Sezer, T Kırkgöz, A Bozaykut International Journal of Pediatrics 2016 (1), 1729218, 2016 | 6 | 2016 |
| Rare cause of severe hypertension in an adolescent boy presenting with short stature: Answers Z Yavas Abali, G Yesil, T Kirkgoz, N Cicek, H Alpay, S Turan, A Bereket, ... Pediatric Nephrology 35, 405-407, 2020 | 4 | 2020 |
| Molecular analysis of MKRN3 gene in Turkish girls with sporadic and familial idiopathic central precocious puberty T Kırkgöz, SB Kaygusuz, C Alavanda, D Helvacıoğlu, ZY Abalı, BG Tosun, ... Journal of Pediatric Endocrinology and Metabolism 36 (4), 401-408, 2023 | 3 | 2023 |
| An 18 month old boy with hypoglycemic convulsion and obesity due to POMC deficiency SB Kaygusuz, G Yesil, T Kirkgoz, S Turan, A Bereket, T Guran Hormone Research in Paediatrics: 57th Annual Meeting of the European Society …, 2018 | 2 | 2018 |
| Evaluation of Serum Advanced Glycation End Product Levels and Microvascular Complications in Children and Adolescents with Type 1 Diabetes Mellitus T Kırkgöz, S Acar, T Küme, HH Kırkgöz, G Tabanlı, Ö Nalbantoğlu, ... Turkish Archives of Pediatrics 59 (1), 31, 2024 | 1 | 2024 |
| Genetic diagnosis of congenital hypopituitarism in Turkish patients by a target gene panel: novel pathogenic variants in GHRHR, GLI2, LHX4 and POU1F1 genes T Kırkgöz, S Gürsoy, S Acar, Ö Nalbantoğlu, B Özkaya, HA Korkmaz, ... Archives of Endocrinology and Metabolism 68, e220254, 2023 | 1 | 2023 |
| Could hematologic parameters have a predictive role in pediatric hashimoto thyroiditis? T Kirkgöz, B Özkan | 1 | 2022 |
| A Null Mutation of TNFRSF11A Causes Dysosteosclerosis, Not Osteopetrosis T Kırkgöz, B Özkan, F Hazan, S Acar, Ö Nalbantoğlu, B Özkaya, MA Kulalı, ... Frontiers in Genetics 13, 938814, 2022 | 1 | 2022 |
| Familial Hypomagnesemia with Hypercalciuria and Nephrocalcinosis Due to CLDN16 Gene Mutations: Novel Findings in Two Cases with Diverse Clinical Features M Eltan, Z Yavas Abali, A Turkyilmaz, I Gokce, S Abali, C Alavanda, ... Calcified tissue international, 1-10, 2022 | 1 | 2022 |
| Efficacy of the Novel Degludec/Aspart Insulin Co-formulation in Children and Adolescents with Type 1 Diabetes: A Real-life Experience with One Year of IDegAsp Therapy in Poorly … T Kırkgöz, M Eltan, SB Kaygusuz, ZY Abalı, D Helvacıoğlu, TS Menevşe, ... Journal of Clinical Research in Pediatric Endocrinology 14 (1), 10, 2022 | 1 | 2022 |
| Efficacy of the Novel Degludec/Aspart Insulin Co-formulation in Children and Adolescents with Type 1 Diabetes: A Real-life Experience with 1-year IDeg/Asp Therapy in Poorly … T Kirkgoz, M Eltan, S Kaygusuz, Z Yavas Abali, D Helvacioglu, ... Journal of clinical research in pediatric endocrinology 14, 2022 | 1 | 2022 |
