| The clinical and genetic heterogeneity of mixed gonadal dysgenesis: does “disorders of sexual development (DSD)” classification based on new Chicago consensus cover all sex … G Öcal, M Berberoğlu, Z Şıklar, HI Ruhi, A Tükün, E Çamtosun, ŞS Erdeve, ... European journal of pediatrics 171, 1497-1502, 2012 | 42 | 2012 |
| Diagnostic characteristics and metabolic risk factors of cases with polycystic ovary syndrome during adolescence Z Sıklar, M Berberoğlu, E Çamtosun, P Kocaay Journal of pediatric and adolescent gynecology 28 (2), 78-83, 2015 | 40 | 2015 |
| ROHHAD syndrome: reasons for diagnostic difficulties in obesity P Kocaay, Z Şıklar, E Çamtosun, T Kendirli, M Berberoğlu Journal of Clinical Research in Pediatric Endocrinology 6 (4), 254, 2014 | 35 | 2014 |
| Gonadotropin-releasing hormone analogue treatment in females with moderately early puberty: no effect on final height Ş Savaş-Erdeve, Z Şıklar, B Hacıhamdioğlu, P Kocaay, E Çamtosun, ... Journal of clinical research in pediatric endocrinology 8 (2), 211, 2016 | 28 | 2016 |
| Novel mutations in obesity-related genes in Turkish children with non-syndromic early onset severe obesity: a multicentre study A Akıncı, D Türkkahraman, İ Tekedereli, L Özer, B Evren, İ Şahin, T Kalkan, ... Journal of clinical research in pediatric endocrinology 11 (4), 341, 2019 | 27 | 2019 |
| Clinical review of 95 patients with 46, XX disorders of sex development based on the new Chicago classification G Öcal, M Berberoğlu, Z Sıklar, Z Aycan, B Hacıhamdioglu, ŞS Erdeve, ... Journal of pediatric and adolescent gynecology 28 (1), 6-11, 2015 | 27 | 2015 |
| Preperitoneal fat tissue may be associated with arterial stiffness in obese adolescents B Hacıhamdioğlu, G Öçal, M Berberoğlu, Z Şıklar, S Fitöz, E Tutar, ... Ultrasound in Medicine & Biology 40 (5), 871-876, 2014 | 22 | 2014 |
| The association between premature adrenarche and cardiovascular risk may be greater than expected N Çelik, H Alp, E Çamtosun, E Alp, S Çelik, E Berk Hormone Research in Paediatrics 87 (1), 7-14, 2017 | 21 | 2017 |
| A novel heterozygous mutation in steroidogenic factor-1 in pubertal virilization of a 46, XY female adolescent Z Sıklar, M Berberoğlu, S Ceylaner, E Çamtosun, P Kocaay, G Göllü, ... Journal of pediatric and adolescent gynecology 27 (2), 98-101, 2014 | 20 | 2014 |
| A deep intronic HADH splicing mutation (c. 636+ 471G> T) in a congenital hyperinsulinemic hypoglycemia case: long term clinical course E Çamtosun, SE Flanagan, S Ellard, Z Şıklar, K Hussain, P Kocaay, ... Journal of clinical research in pediatric endocrinology 7 (2), 144, 2015 | 16 | 2015 |
| The effect of recombinant growth hormone treatment in children with idiopathic short stature and low insulin-like growth factor-1 levels Z Siklar, P Kocaay, E Çamtosun, M İsakoca, B Hacihamdioglu, SS Erdeve, ... Journal of Clinical Research in Pediatric Endocrinology 7 (4), 2015 | 13 | 2015 |
| Pediatric primary adrenal insufficiency: a 21-year single center experience E Çamtosun, İ Dündar, A Akıncı, L Kayaş, N Çiftci Journal of clinical research in pediatric endocrinology 13 (1), 88, 2021 | 12 | 2021 |
| A case of cleidocranial dysplasia with a novel mutation and growth velocity gain with growth hormone treatment E Çamtosun, A Akıncı, E Demiral, İ Tekedereli, A Sığırcı Journal of Clinical Research in Pediatric Endocrinology 11 (3), 301, 2019 | 12 | 2019 |
| Coexistence of mosaic uniparental isodisomy and a KCNJ11 mutation presenting as diffuse congenital hyperinsulinism and hemihypertrophy P Kocaay, Z Şiklar, S Ellard, A Yagmurlu, E Çamtosun, E Erden, ... Hormone research in paediatrics 85 (6), 421-425, 2016 | 12 | 2016 |
| The evaluation of thyroid carcinoma in childhood and concomitance of autoimmune thyroid disorders B Hacıhamdioğlu, G Öçal, M Berberoğlu, ŞS Erdeve, E Çamtosun, ... Journal of Pediatric Endocrinology and Metabolism 27 (9-10), 901-908, 2014 | 11 | 2014 |
| Response to anastrozole treatment in a case with peutz-jeghers syndrome and a large cell calcifying Sertoli cell tumor MK Yekedüz, Z Şıklar, B Burgu, Z Kuloğlu, P Kocaay, E Çamtosun, ... Journal of Clinical Research in Pediatric Endocrinology 9 (2), 168, 2017 | 9 | 2017 |
| Delayed diagnosis of a 17-hydroxylase/17, 20-lyase deficient patient presenting as a 46, XY female: a low normal potassium level can be an alerting diagnostic sign E Çamtosun, Z Şıklar, S Ceylaner, P Kocaay, M Berberoğlu Journal of Clinical Research in Pediatric Endocrinology 9 (2), 163, 2017 | 8 | 2017 |
| Three cases of Wolfram syndrome with different clinical aspects E Çamtosun, Z Şıklar, P Kocaay, S Ceylaner, SE Flanagan, S Ellard, ... Journal of Pediatric Endocrinology and Metabolism 28 (3-4), 433-438, 2015 | 8 | 2015 |
| Autosomal recessive cutis laxa: A novel mutation in the FBLN5 gene in a family I Tekedereli, E Demiral, IK Gokce, Z Esener, E Camtosun, A Akinci Clinical Dysmorphology 28 (2), 63-65, 2019 | 6 | 2019 |
| Prospective follow-up of children with idiopathic growth hormone deficiency after termination of growth hormone treatment: is there really need for treatment at transition to … E Çamtosun, Z Şıklar, M Berberoğlu Journal of Clinical Research in Pediatric Endocrinology 10 (3), 247, 2018 | 6 | 2018 |
