Effects of iron deficiency anemia on hemoglobin A1c in type 1 diabetes mellitus Ö Tarim, A Küçükerdogan, Ü Günay, Ö Eralp, İ Ercan Pediatrics international 41 (4), 357-362, 1999 | 298 | 1999 |
Rare causes of primary adrenal insufficiency: genetic and clinical characterization of a large nationwide cohort T Guran, F Buonocore, N Saka, MN Ozbek, Z Aycan, A Bereket, F Bas, ... The Journal of Clinical Endocrinology & Metabolism 101 (1), 284-292, 2016 | 162 | 2016 |
Nutrition in adolescence F Lifshitz, O Tarim, MM Smith Endocrinology and metabolism clinics of North America 22 (3), 673-683, 1993 | 137 | 1993 |
Thyroid hormones and growth in health and disease Ö Tarım Journal of clinical research in pediatric endocrinology 3 (2), 51, 2011 | 90 | 2011 |
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 |
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 |
Prevalence and correlates of obesity in schoolchildren from the city of Bursa, Turkey J Endo J Clin Res Ped Endo 1 (2), 80-8, 2008 | 63 | 2008 |
Homozygous loss-of-function mutations in SLC26A7 cause goitrous congenital hypothyroidism H Cangul, XH Liao, E Schoenmakers, J Kero, S Barone, P Srichomkwun, ... JCI insight 3 (20), 2018 | 59 | 2018 |
Considerations about dietary fat restrictions for children F Lifshitz, O Tarim The Journal of nutrition 126, 1031S-1041S, 1996 | 55 | 1996 |
Clinical course of hyperprolactinemia in children and adolescents: a review of 21 cases E Eren, Ş Yapıcı, EDP Çakır, LA Ceylan, H Sağlam, Ö Tarım Journal of clinical research in pediatric endocrinology 3 (2), 65, 2011 | 53 | 2011 |
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 |
Increased incidence of congenital hypothyroidism due to iodine deficiency H SAG˘ LAM, L Büyükuysal, N Köksal, IL Ercan, Ö Tarim Pediatrics International 49 (1), 76-79, 2007 | 48 | 2007 |
Testicular adrenal rest tumors in patients with congenital adrenal hyperplasia. ED Cakir, FS Mutlu, E Eren, AO Paşa, H Sağlam, O Tarim Journal of clinical research in pediatric endocrinology 4 (2), 94-100, 2012 | 46 | 2012 |
Congenital hypothyroidism in Turkey: a retrospective evaluation of 1000 cases. OF Tarim, N Yordam The Turkish journal of pediatrics 34 (4), 197-202, 1992 | 44 | 1992 |
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 |
Nutritional growth retardation F Lifshitz, O Tarim, M Smith Pediatric Endocrinology: A clinical guide 3, 1996 | 30 | 1996 |
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 |
Clinical and laboratory characteristics of hyperprolactinemia in children and adolescents: national survey E Eren, AT Ergür, ŞP İşgüven, EÇ Bitkin, M Berberoğlu, Z Şıklar, F Baş, ... Journal of clinical research in pediatric endocrinology 11 (2), 149, 2019 | 25 | 2019 |
Mutational analysis of PHEX, FGF23 and CLCN5 in patients with hypophosphataemic rickets A Guven, RA Al‐Rijjal, HA BinEssa, D Dogan, Y Kor, M Zou, N Kaya, ... Clinical endocrinology 87 (1), 103-112, 2017 | 25 | 2017 |
Height predictions by Bayley-Pinneau method may misguide pediatric endocrinologists O Tarim Turk J Pediatr 55 (5), 485-492, 2013 | 24 | 2013 |