| Prevalence and long‐term follow‐up outcomes of testicular adrenal rest tumours in children and adolescent males with congenital adrenal hyperplasia Z Aycan, VN Bas, S Cetinkaya, S Yilmaz Agladioglu, T Tiryaki Clinical endocrinology 78 (5), 667-672, 2013 | 91 | 2013 |
| Prader-Willi syndrome and growth hormone deficiency Z Aycan, VN Baş Journal of clinical research in pediatric endocrinology 6 (2), 62, 2014 | 89 | 2014 |
| Adherence to growth hormone therapy: results of a multicenter study BK Aydın, Z Aycan, Z Şıklar, M Berberoğlu, G Öcal, S Çetinkaya, VN Baş, ... Endocrine Practice 20 (1), 46-51, 2014 | 78 | 2014 |
| 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 | 77 | 2015 |
| Thyroid dyshormonogenesis is mainly caused by TPO mutations in consanguineous community H Cangul, Z Aycan, A Olivera‐Nappa, H Saglam, NA Schoenmakers, ... Clinical endocrinology 79 (2), 275-281, 2013 | 75 | 2013 |
| Effects of vitamin D levels on asthma control and severity in pre-school children A Turkeli, O Ayaz, A Uncu, B Özhan, VN Bas, AK Tufan, O Yilmaz European review for medical and pharmacological sciences, 2016 | 72 | 2016 |
| Assessment of the knowledge of diabetes mellitus among school teachers within the scope of the managing diabetes at school program Z Aycan, A Önder, S Çetinkaya, H Bilgili, N Yıldırım, VN Baş, ... Journal of Clinical Research in Pediatric Endocrinology 4 (4), 199, 2012 | 66 | 2012 |
| Diverse genotypes and phenotypes of three novel thyroid hormone receptor-α mutations K Demir, ALM van Gucht, M Büyükinan, G Çatlı, Y Ayhan, VN Baş, ... The Journal of Clinical Endocrinology & Metabolism 101 (8), 2945-2954, 2016 | 64 | 2016 |
| Digenic DUOX1 and DUOX2 Mutations in Cases With Congenital Hypothyroidism Z Aycan, H Cangul, M Muzza, VN Bas, L Fugazzola, VK Chatterjee, ... The Journal of Clinical Endocrinology & Metabolism 102 (9), 3085-3090, 2017 | 55 | 2017 |
| Targeted multi-gene panel testing for the diagnosis of Bardet Biedl syndrome: identification of nine novel mutations across BBS1, BBS2, BBS4, BBS7, BBS9, BBS10 genes AE Solmaz, H Onay, T Atik, A Aykut, MC Gunes, OO Yuregir, VN Bas, ... European journal of medical genetics 58 (12), 689-694, 2015 | 54 | 2015 |
| Novel TSHR mutations in consanguineous families with congenital nongoitrous hypothyroidism H Cangul, NV Morgan, JR Forman, H Saglam, Z Aycan, T Yakut, T Gulten, ... Clinical endocrinology 73 (5), 671-677, 2010 | 52 | 2010 |
| Maturity onset diabetes of youth (MODY) in Turkish children: sequence analysis of 11 causative genes by next generation sequencing SY Ağladıoğlu, Z Aycan, S Çetinkaya, VN Baş, A Önder, ... Journal of Pediatric Endocrinology and Metabolism 29 (4), 487-496, 2016 | 49 | 2016 |
| Insulin oedema in newly diagnosed type 1 diabetes mellitus VN Baş, S Çetinkaya, SY Ağladıoğlu, HNP Kendirici, H Bilgili, N Yıldırım, ... Journal of clinical research in pediatric endocrinology 2 (1), 46, 2010 | 46 | 2010 |
| Evaluation of factors affecting quality of life in children with type 1 diabetes mellitus V Bas, A Bideci, A SOYSAL ACAR, M ÇAMURDAN, P CİNAZ Journal of Diabetes Metabolism 2 (8), 2011 | 35 | 2011 |
| TSHR is the main causative locus in autosomal recessively inherited thyroid dysgenesis H Cangul, Z Aycan, H Saglam, JR Forman, S Cetinkaya, O Tarim, E Bober, ... Journal of Pediatric Endocrinology and Metabolism 25 (5-6), 419-426, 2012 | 30 | 2012 |
| Short-and long-term effects of individualized enteral protein supplementation in preterm newborns E Ergenekon, E Koç, E Önal, C Türkyılmaz, E Kazancı, S Beken, Ö Turan, ... The Turkish Journal of Pediatrics 55 (4), 365-370, 2013 | 29 | 2013 |
| Thiamine-responsive megaloblastic anemia syndrome with atrial standstill: a case report Z Aycan, VN Bas, S Cetinkaya, SY Agladioglu, HNP Kendirci, F Senocak Journal of Pediatric Hematology/Oncology 33 (2), 144-147, 2011 | 29 | 2011 |
| Bone mineral density and bone metabolic markers’ status in children with neurofibromatosis type 1 HG Poyrazoğlu, VN Baş, A Arslan, F Bastug, M Canpolat, H Per, H Gümüs, ... Journal of Pediatric Endocrinology and Metabolism 30 (2), 175-180, 2017 | 27 | 2017 |
| Diseases accompanying congenital hypothyroidism VN Baş, Ş Özgelen, S Çetinkaya, Z Aycan Journal of Pediatric Endocrinology and Metabolism 27 (5-6), 485-489, 2014 | 27 | 2014 |
| Diabetic euglycemic ketoacidosis in newly diagnosed type 1 diabetes mellitus during Ramadan fasting VN Baş, S Uytun, YA Torun Journal of Pediatric Endocrinology and Metabolism 28 (3-4), 333-335, 2015 | 25 | 2015 |
