Sitting height and sitting height/height ratio references for Turkish children R Bundak, F Bas, A Furman, H Günöz, F Darendeliler, N Saka, ... European journal of pediatrics 173, 861-869, 2014 | 105 | 2014 |
Constitutional delay of growth and puberty: from presentation to final height Ş Poyrazoglu, H Günöz, F Darendeliler, Ν Saka, R Bundak, F Baş Journal of Pediatric Endocrinology and Metabolism 18 (2), 171-180, 2005 | 84 | 2005 |
Turner syndrome and associated problems in Turkish children: a multicenter study E Yeşilkaya, A Bereket, F Darendeliler, F Baş, Ş Poyrazoğlu, BK Aydın, ... Journal of Clinical Research in Pediatric Endocrinology 7 (1), 27, 2015 | 78 | 2015 |
Cleidocranial dysplasia: clinical, endocrinologic and molecular findings in 15 patients from 11 families FD Bir, N Dinçkan, Y Güven, F Baş, U Altunoğlu, SS Kuvvetli, ... European journal of medical genetics 60 (3), 163-168, 2017 | 44 | 2017 |
Distribution of gene mutations associated with familial normosmic idiopathic hypogonadotropic hypogonadism F Gürbüz, LD Kotan, E Mengen, Z Şıklar, M Berberoğlu, S Dökmetaş, ... Journal of clinical research in pediatric endocrinology 4 (3), 121, 2012 | 37 | 2012 |
Klinefelter syndrome in childhood: variability in clinical and molecular findings N Akcan, Ş Poyrazoğlu, F Baş, R Bundak, F Darendeliler Journal of clinical research in pediatric endocrinology 10 (2), 100, 2018 | 35 | 2018 |
The growth characteristics of patients with noonan syndrome: results of three years of growth hormone treatment: a nationwide multicenter study Z Şıklar, M Genens, Ş Poyrazoğlu, F Baş, F Darendeliler, R Bundak, ... Journal of Clinical Research in Pediatric Endocrinology 8 (3), 305, 2016 | 32 | 2016 |
Prevalence, clinical characteristics and long-term outcomes of classical 11 β-hydroxylase deficiency (11BOHD) in Turkish population and novel mutations in CYP11B1 gene F Baş, G Toksoy, B Ergun-Longmire, ZO Uyguner, ZY Abalı, Ş Poyrazoğlu, ... The Journal of steroid biochemistry and molecular biology 181, 88-97, 2018 | 30 | 2018 |
Incidence of type 1 diabetes in children aged below 18 years during 2013-2015 in northwest Turkey Ş Poyrazoğlu, R Bundak, ZY Abalı, H Önal, S Sarıkaya, A Akgün, S Baş, ... Journal of clinical research in pediatric endocrinology 10 (4), 336, 2018 | 28 | 2018 |
A rare cause of congenital adrenal hyperplasia: clinical and genetic findings and follow-up characteristics of six patients with 17-hydroxylase deficiency including two novel … AD Kardelen, G Toksoy, F Baş, ZY Abalı, G Gençay, Ş Poyrazoğlu, ... Journal of Clinical Research in Pediatric Endocrinology 10 (3), 206, 2018 | 27 | 2018 |
Two novel mutations in XYLT2 cause spondyloocular syndrome F Taylan, Z Yavaş Abalı, N Jaentti, N Güneş, F Darendeliler, F Baş, ... American Journal of Medical Genetics Part A 173 (12), 3195-3200, 2017 | 26 | 2017 |
Clinicopathological characteristics of papillary thyroid cancer in children with emphasis on pubertal status and association with BRAFV600E mutation Ş Poyrazoğlu, R Bundak, F Baş, G Yeğen, Y Şanlı, F Darendeliler Journal of clinical research in pediatric endocrinology 9 (3), 185, 2017 | 25 | 2017 |
Frequency and severity of ketoacidosis at onset of autoimmune type 1 diabetes over the past decade in children referred to a tertiary paediatric care centre: potential impact … A Uçar, N Saka, F Baş, M Sukur, S Poyrazoğlu, F Darendeliler, R Bundak Journal of Pediatric Endocrinology and Metabolism 26 (11-12), 1059-1065, 2013 | 24 | 2013 |
Associations of size at birth and postnatal catch-up growth status with clinical and biomedical characteristics in prepubertal girls with precocious adrenarche: preliminary results A Uçar, M Yackobovitch-Gavan, OB Erol, E Yekeler, N Saka, F Baş, ... The Journal of Clinical Endocrinology & Metabolism 99 (8), 2878-2886, 2014 | 23 | 2014 |
Evaluation of diagnosis and treatment results in children with Graves' disease with emphasis on the pubertal status of patients Ş Poyrazoğlu, N Saka, F Bas, P Isguven, A Dogu, S Turan, A Turan, ... Journal of Pediatric Endocrinology and Metabolism 21 (8), 745-752, 2008 | 23* | 2008 |
Assessment of paediatric Hashimoto's thyroiditis using superb microvascular imaging Z Bayramoglu, SG Kandemirli, E Caliskan, R Yilmaz, AD Kardelen, ... Clinical Radiology 73 (12), 1059. e9-1059. e15, 2018 | 22 | 2018 |
Sonography and magnetic resonance imaging characteristics of testicular adrenal rest tumors R Yılmaz, D Şahin, A Aghayev, OB Erol, Ş Poyrazoğlu, N Saka, E Yekeler Polish journal of radiology 82, 583, 2017 | 22 | 2017 |
Current practice in diagnosis and treatment of growth hormone deficiency in childhood: a survey from Turkey Ş Poyrazoğlu, T Akcay, İ Arslanoğlu, ME Atabek, Z Atay, M Berberoğlu, ... Journal of clinical research in pediatric endocrinology 7 (1), 37, 2015 | 22 | 2015 |
Clinical, biochemical and genetic features with nonclassical 21-hydroxylase deficiency and final height Ş Savaş-Erdeve, S Çetinkaya, ZY Abalı, Ş Poyrazoğlu, F Baş, ... Journal of Pediatric Endocrinology and Metabolism 30 (7), 759-766, 2017 | 20 | 2017 |
Increased arterial stiffness in young normotensive patients with Turner syndrome: associations with vascular biomarkers A Uçar, F Öz, F Baş, H Oflaz, K Nişli, M Tuğrul, A Yetim, F Darendeliler, ... Clinical Endocrinology 82 (5), 719-727, 2015 | 20 | 2015 |