Education

1996-2002 Medical Doctor Training, Istanbul University Cerrahpaşa Faculty of Medicine

2004-2010 Medical Specialization in Pediatrics, Istanbul Bakırköy Women's and Children's Health Training and Research Hospital

2011-2014 Subspecialty in Pediatric Endocrinology, Eskişehir Osmangazi University Faculty of Medicine

Institutions Worked

2010-2011 Specialist Doctor, Pediatrics, Tekirdağ Çerkezköy State Hospital

2015-2018 Specialist Doctor, Pediatric Endocrinology, Tekirdağ Çorlu State Hospital

2018-2019 Associate Professor, Pediatric Endocrinology, Tekirdağ Namık Kemal University Faculty of Medicine

Scientific Publications

A. Articles published in international peer-reviewed journals:

A1. Taşkın U, Binay O, Binay C, Yigit O. Post tonsillectomy rapidly developing iatrogenic hyponatremia in a child. Ear Nose Throat J. 2012;91(11):486-7.

A2. Simsek E, Binay C, Ceylaner S. The earlier described mutation (c.307c > T [p.R103X]) in the SRD5A2 gene causing a 46,XY female phenotype. J Pediatr Endocrinol Metab. 2012;25(5-6):543-5.

A3. Şimşek E, Binay Ç, Flanagan SE, Ellard S, Hussain K, Kabukçuoğlu S. Congenital hyperinsulinism presenting with different clinical, biochemical and molecular genetic spectra. Turk J Pediatr. 2013;55(6):584-90.

A4. Binay C, Simsek E, Cilingir O, Yuksel Z, Kutlay O, Artan S. Prevalence of nonclassic congenital adrenal hyperplasia in Turkish children presenting with premature pubarche, hirsutism, or oligomenorrhoea. Int J Endocrinol. 2014;2014:768506.

A5. Binay C, Simsek E, Bal C. The correlation between GnRH stimulation testing and obstetric ultrasonographic parameters in precocious puberty. J Pediatr Endocrinol Metab. 2014;27(11-12):1193-9.

A6. Simsek E, Binay C, Ilhan H, Ihtiyar E, Demiral M, Aksivrikoz I, Dündar E, Akcar N. Metastatic papillary thyroid carcinoma in an autonomous hyperfunctioning thyroid nodule in an adolescent: case report and literature review. Thyroid Disorders Ther 2014;3:2.

A7. Darendeliler F, Yeşilkaya E, Bereket A, Baş F, Bundak R, Sarı E, Küçükemre Aydın B, Darcan Ş, Dündar B, Büyükinan M, Kara C, Mazıcıoğlu MM, Adal E, Akıncı A, Atabek ME, Demirel F, Çelik N, Özkan B, Özhan B, Orbak Z, Ersoy B, Doğan M, Ataş A, Turan S, Gökşen D, Tarım Ö, Yüksel B, Ercan O, Hatun Ş, Şimşek E, Ökten A, Abacı A, Döneray H, Özbek MN, Keskin M, Önal H, Akyürek N, Bulan K, Tepe D, Emeksiz HC, Demir K, Kızılay D, Topaloğlu AK, Eren E, Özen S, Demirbilek H, Abalı S, Akın L, Eklioğlu BS, Kaba S, Anık A, Baş S, Ünüvar T, Sağlam H, Bolu S, Özgen T, Doğan D, Çakır ED, Şen Y, Andıran N, Çizmecioğlu F, Evliyaoğlu O, Karagüzel G, Pirgon Ö, Çatlı G, Can HD, Gürbüz F, Binay Ç, Baş VN, Sağlam C, Gül D, Polat A, Açıkel C, Cinaz P. Growth curves for Turkish Girls with Turner Syndrome: Results of the Turkish Turner Syndrome Study Group. Clin Res Pediatr Endocrinol. 2015;7(3):183-91.

A8. Binay C, Simsek E, Yıldırım A, Kosger P, Demiral M, Kılıç Z. Growth hormone and the risk of atherosclerosis in growth hormone-deficient children. Growth Horm IGF Res. 2015; 25(6): 294-7.

A9. Yeşilkaya E, Bereket A, Darendeliler F, Baş F, Poyrazoğlu Ş, Küçükemre Aydın B, Darcan Ş, Dündar B, Büyükinan M, Kara C, Sarı E, Adal E, Akıncı A, Atabek ME, Demirel F, Çelik N, Özkan B, Özhan B, Orbak Z, Ersoy B, Doğan M, Ataş A, Turan S, Gökşen D, Tarım Ö, Yüksel B, Ercan O, Hatun Ş, Şimşek E, Ökten A, Abacı A, Döneray H, Özbek MN, Keskin M, Önal H, Akyürek N, Bulan K, Tepe D, Emeksiz HC, Demir K, Kızılay D, Topaloğlu AK, Eren E, Özen S, Abalı S, Akın L, Selver Eklioğlu B, Kaba S, Anık A, Baş S, Ünüvar T, Sağlam H, Bolu S, Özgen T, Doğan D, Deniz Çakır E, Şen Y, Andıran N, Çizmecioğlu F, Evliyaoğlu O, Karagüzel G, Pirgon Ö, Çatlı G, Can HD, Gürbüz F, Binay Ç,Baş VN, Fidancı K, Polat A, Gül D, Açıkel C, Demirbilek H, Cinaz P, Bondy C. Turner syndrome and associated problems in Turkish children: a multicenter study. J Clin Res Pediatr Endocrinol. 2015;7(1):27-36.

A10. Şimşek E, Binay C. Premature menarche associated with McCune-Albright syndrome in an infant. Journal of Clinical Research in Pediatric Endocrinology, 2015;7 (suppl1):22.

A11. Şahin S, Binay C, Şimşek E, Dinleyici EC, Çarman KB. Hyperglycemia After Metformin Overdose: A Case Report. Int J Clin Pediatr 2016; 5: 44-46.

A12. Uğurlu V, Binay C, Şimşek E, Bal C. Cellular Trace Element Changes in Type 1 Diabetes Patients. J Clin Res Pediatr Endocrinol 2016;8(2):180-6.

A13. Sari E, Bereket A, Yeşilkaya E, Baş F, Bundak R, Aydın BK, Darcan Ş, Dündar B, Büyükinan M, Kara C, Adal E, Akıncı A, Atabek ME, Demirel F, Çelik N, Özkan B, Özhan B, Orbak Z, Ersoy B, Doğan M, Ataş A, Turan S, Gökşen D, Tarım Ö, Yüksel B, Ercan O, Hatun Ş, Şimşek E, Ökten A, Abacı A, Döneray H, Özbek MN, Keskin M, Önal H, Akyürek N, Bulan K, Tepe D, Emeksiz HC, Demir K, Kızılay D, Topaloğlu AK, Eren E, Özen S, Demirbilek H, Abalı S, Akın L, Eklioğlu BS, Kaba S, Anık A, Baş S, Ünüvar T, Sağlam H, Bolu S, Özgen T, Doğan D, Çakır ED, Şen Y, Andıran N, Çizmecioğlu F, Evliyaoğlu O, Karagüzel G, Pirgon Ö, Çatlı G, Can HD, Gürbüz F, Binay Ç, Baş VN, Fidancı K, Gül D, Polat A, Açıkel C, Cinaz P, Darendeliler F. Anthropometric findings from birth to adulthood and their relation with karyotype distribution in Turkish girls with Turner syndrome. Am J Med Genet A. 2016;170(4):942-8.

A14. Şimşek E, Montenegro LR, Binay C, Demiral M, Acıkalin MF, Latronico AC. Clinical and Hormonal Features of a Male Adolescent with Congenital Isolated Follicle-Stimulating Hormone Deficiency. Horm Res Paediatr. 2016;85(3):207-12.

A15. Şimşek E, Binay C, Demiral M, Tokar B, Kabukcuoglu S, Ustun M. Gonadoblastoma and papillary tubal hyperplasia in ovotesticular syndrome. J Clin Res Pediatr Endocrinol. 2016;8(3):351-5.

A16. Hatun Ş, Demirbilek H, Darcan Ş, Yüksel A, Binay C, Şimşek DG, Kara C, Çetinkaya E, Ünüvar T, Uçaktürk A, Tütüncüler F, Cesur Y, Bundak R, Sağlam H, Şimşek E, Bereket A; Turkish Pediatric Diabetes Research Group. Evaluation of therapeutic management patterns and glycemic control of pediatric type 1 diabetes mellitus patients in Turkey: A nationwide cross-sectional study. Diabetes Res Clin Pract. 2016;119:32-40.

A17. Binay C, Kavuncuoğlu S, Fidan V, Binay O, Altuncu E, Taşkın U. Screening for Abnormal Hearing in Newborns and Assessment of High-Risk Group. Austin J Otolaryngol 2016; 3(2): id1073.

A18. Demiral M, Binay C, Şimşek E, İlhan H. Horner Syndrome Secondary to Thyroid Surgery. Case Rep Endocrinol. 2017;2017:1689039.

A19. Binay C, Paketçi C, Güzel S, Samancı N. Irisin and Oxytocin as Predictors of Metabolic Parameters in Obese Children. J Clin Res Pediatr Endocrinol. 2017; 9(2): 124-131.

A20. Binay C, Bozkurt Turhan A, Şimşek E, Bor Ö, Akay M. Evaluation of Coagulation Profile in Children with Type 1 Diabetes Mellitus Using Rotational Thromboelastometry. Indian J Hematol Blood Transfus 2017, 33(4): 574-580.

A21. Poyrazoğlu Ş, Bundak R, Yavaş Abalı Z, Önal H, Sarıkaya S, Akgün A, Baş S, Abalı S, Bereket A, Eren E, Tarım Ö, Güven A, Yıldız M, Karaman Aksakal D, Yüksel A, Seymen Karabulut G, Hatun Ş, Özgen T, Cesur Y, Azizoğlu M, Dilek E, Tütüncüler F, Papatya Çakır E, Özcabı B, Evliyaoğlu O, Karadeniz S, Çizmecioğlu F, Açıkel C, Kula M, Demirel F, Baş VN, Orbak Z, Binay Ç, Turan S, Çetinkaya S, Asan O, Abacı A, Çatlı G, Demir K, Gökşen D, Dağdelen A, Demirbilek H, Darendeliler F. Frequency and risk factors of metabolic syndrome in obese children: the findings of a multicenter study in Turkey. J Clin Res Pediatr Endocrinol. 2018;10(3): 228-240.

A22. Akbaş E, Aydoğan Uslu Ü, Emek E, Binay Ç, Paketçi C, Güzel S, Paketçi Aİ, Zülfikar B. Association between vitamin D deficiency and puberty timing in overweight and obese children. J Clin Res Pediatr Endocrinol. 2019;11(3):217-225.

A23. Binay Ç, Gürkan Y, Demiral M, Tepe D, Şimşek E. Evaluation of hypothalamic-pituitary axis in children and adolescents with thalassemia major. J Clin Res Pediatr Endocrinol. 2019;11(4):335-342.

B. Articles Published in National Peer-Reviewed Journals:

B1. Karabayır N, Adal E, Binay Ç. A rare presentation of adrenal hemorrhage in a newborn: case report. Türkiye Klinikleri J Med Sci 2010;30(5):1768-71.

B2. Binay Ç, Tunca Şahin G, Biçer S, Gemici H, Şahin S, Bahar S, Şiraneci R, Engerek N. Evaluation of poisoning cases in the pediatric emergency unit in 2006. Akademik Acil Tıp Dergisi 2010;9(1):31-40.

B3. Binay Ç, Kirel B. Frequency of metabolic syndrome in obese children presenting to our Endocrinology Clinic. Turkish J Pediatr Dis 2013;2:79-85.

B4. Binay Ç, Şimşek E. Mauriac syndrome presenting with generalized edema. Türkiye Klinikleri J Pediatr 2014;23(1):43-8.

B5. Simsek E, Binay Ç, Gobüt N. Fibrodysplasia Ossificans Progressiva: A case presentation. J Curr Pediatr 2015;13:222-6.

B6. Binay Ç, Simsek E. Hashimoto's Thyroiditis in Children and Adolescents. Osmangazi Tıp Dergisi/Osmangazi Journal of Medicine 2016;38(2):1-8.

B7. Demiral M, Binay Ç, Simsek E. Epidemiological characteristics of patients diagnosed with Type 1 Diabetes Mellitus in Eskişehir Province. Çocuk Sağlığı ve Hastalıkları Dergisi 2016;59:14-20.

B8. Binay Ç, Simsek E, Tekin N, Demiral M. Neonatal hypercalcemia associated with congenital adrenal hyperplasia. J Exp Clin Med 2017;34(3):223-225.

B9. Turhan AB, Binay Ç, Bor O, Simsek E. The effects of short-term use of granulocyte colony-stimulating factor on bone metabolism in child cancer patients. North Clin Istanb 2018 Dec 3;5(4):277-281.

C. Presentations at National and International Symposiums, Congresses, or Conferences:

C. Poster presentations published in the proceedings of national scientific meetings:

C1. Adal E, Önal H, Karabulut M, Binay Ç, Önal Z. Congenital lymphedema and chylothorax. 44th Turkish Pediatric Congress, Istanbul, June 14-18, 2008.

C2. Adal E, Önal H, Binay Ç, Karabulut M. Use of oxcarbazepine during pregnancy and lactation: a case presentation. 44th Turkish Pediatric Congress, Istanbul, June 14-18, 2008.

C3. Binay Ç, Tunca Şahin G, Biçer S, Gemici H, Şahin S, Bahar S, Şiraneci R, Engerek N. Analysis of poisoning cases. 52nd Turkish National Pediatric Congress, Antalya, 2008.

C4. Adal E, Önal H, Karabulut M, Binay Ç, Aydın A. Isovaleric acidemia in the etiology of recurrent diarrhea and dehydration. 44th Turkish Pediatric Congress, Istanbul, June 14-18, 2008.

C5. Önal H, Adal E, Binay Ç, Karabulut M, Aydın A. Lysinuric protein intolerance mimicking Hirschsprung's disease. 44th Turkish Pediatric Congress, Istanbul, June 14-18, 2008.

C6. Şimşek E, Binay Ç, Göbüt N. Spontaneous ovarian hyperstimulation syndrome: FSH receptor activation mutation? 15th National Pediatric Endocrinology and Diabetes Congress, Izmir, November 22-23, 2011.

C7. Binay Ç, Kırel B. Prevalence of metabolic syndrome in obese children. 15th National Pediatric Endocrinology and Diabetes Congress, Izmir, November 22-23, 2011.

C8. Binay Ç, Göbüt N, Şimşek E. Testicular agenesis (‘Vanishing testis’ syndrome): two case presentations. 15th National Pediatric Endocrinology and Diabetes Congress, Izmir, November 22-23, 2011.

C9. Şimşek E, Binay Ç, Göbüt N. Fibrodysplasia ossificans progressiva: case presentation. 15th National Pediatric Endocrinology and Diabetes Congress, Izmir, November 22-23, 2011.

C10. Simsek E, Dallar Y, Selver B, Çetinkaya S, Binay Ç, Kocabay K. In Hashimoto's thyroiditis, what TSH response to the TRH test should initiate L-thyroxine therapy? 15th National Pediatric Endocrinology and Diabetes Congress, Izmir, November 22-23, 2011.

C11. Şimşek E, Selver B, Dallar Y, Binay Ç, Bal C. Epidemiology of obesity in children living under low socioeconomic conditions. 16th National Pediatric Endocrinology and Diabetes Congress, Izmir, November 6-10, 2012.

C12. Şimşek E, Binay Ç, Tokar B, Kabukcuoğlu S, Üstün M. SRY positivity and difficulty in sexual preference decision in 46,XX ovotesticular syndrome. 16th National Pediatric Endocrinology and Diabetes Congress, Izmir, November 6-10, 2012.

C13. Şimşek E, Binay Ç, Tokar B, Kabukcuoğlu S, Üstün M. SRY gene expression and ovotesticular sexual differentiation disorder in a patient with 46,XX karyotype; ‘streak’ and ovotesticular gonads in a patient with 46,XY karyotype; dysgerminoma, gonadoblastoma, and papillary tubal hyperplasia. Pediatric Endocrinology Case Presentations 5, Ankara, April 12-13, 2013.

C14. Şimşek E, Binay Ç. Type 1 neurofibromatosis presenting with secondary amenorrhea and severe malabsorption. 17th National Pediatric Endocrinology and Diabetes Congress, Edirne, October 1-5, 2013.

C15. Hatun Ş, Darcan Ş, Gökçen Şimşek D, Şimşek E, Bereket A, Yüksek A, Binay Ç. Family education status and diabetes education in children with Type 1 diabetes. 17th National Pediatric Endocrinology and Diabetes Congress, Edirne, October 1-5, 2013.

C16. Binay Ç, Şimşek E, Bal C. Correlation between obstetric parameters and GnRH stimulation test in the diagnosis of central precocious puberty. 17th National Pediatric Endocrinology and Diabetes Congress, Edirne, October 1-5, 2013.

C17. Hatun Ş, Darcan Ş, Gökçen Şimşek D, Şimşek E, Bereket A, Yüksek A, Binay Ç. Long-term follow-up and metabolic control in children with Type 1 diabetes: the situation in our country. 17th National Pediatric Endocrinology and Diabetes Congress, Edirne, October 1-5, 2013.

C18. Simsek E, Binay Ç, Ağırel B, Demiral M, Köse N. Familial hypophosphatemic rickets: case presentation. Turkish National Pediatric Congress, Antalya, October 22-26, 2014.

C19. Ağırel B, Demiral M, Binay Ç, Şimşek E. Rare association of autoimmune hypophysitis and Type 1 diabetes: Type 1 autoimmune polyglandular syndrome. Turkish National Pediatric Congress, Antalya, October 22-26, 2014.

C20. Demiral M, Simsek E, Binay Ç, Tokar B. Horner's syndrome developing after thyroidectomy in adolescence. National Pediatric Endocrinology and Diabetes Congress, Bursa, November 4-8, 2014.

C21. Simsek E, Binay Ç, Demiral M, Tokar B, Dündar E. A new mutation in exon 5 of the TP53 gene in familial adrenocortical carcinoma. National Pediatric Endocrinology and Diabetes Congress, Bursa, November 4-8, 2014.

C22. Binay Ç, Demiral M, Şimşek E, Ceylaner S. Familial hypocalciuric hypocalcemia associated with A968S polymorphism in the calcium-sensing receptor (CaSR) gene. 19th National Pediatric Endocrinology and Diabetes Congress, Istanbul, October 22-25, 2015.

C23. Demiral M, Binay Ç, Şimşek E. Epidemiological characteristics of patients diagnosed with insulin-dependent diabetes mellitus in Eskişehir Province. 19th National Pediatric Endocrinology and Diabetes Congress, Istanbul, October 22-25, 2015.

C24. Binay Ç, Şimşek E, Demiral M. Rickets-like metaphyseal changes in a patient with MMP13 mutation: Spahr type metaphyseal dysplasia. Pediatric Endocrinology Case Presentations 8, Adana, April 29-30, 2016.

C25. Binay Ç, Paketçi C, Güzel S, Samancı N. Evaluation of the effects of oxytocin and irisin levels on metabolic parameters in obese children. 20th National Pediatric Endocrinology and Diabetes Congress, Antalya, October 5-9, 2016.

C26. Demiral M, Binay C, Şimşek E. Comparison of clinical features at presentation in antibody-positive and negative cases of diabetes mellitus. 1st Diabetes Technology Symposium, Izmir, January 20-22, 2017.

D. Verbal Presentations Presented at National Scientific Meetings and Published in Abstract Books:

D1. Simsek E, Binay Ç, Tokar B, Kabukçuoğlu S. Leydig cell hypoplasia: LH receptor inactivation mutation. Pediatric Endocrinology Case Presentations 4, Eskişehir, April 27-29, 2012.

D2. Şahin S, Binay Ç, Simsek E, Dinleyici EÇ. Fatal pancreatitis secondary to metformin intoxication for suicide purposes. Pediatric Endocrinology Case Presentations 4, Eskişehir, April 27-29, 2012.

D3. Simsek E, Kara Y, Binay Ç. Hyporeninemic hypoaldosteronism. Pediatric Endocrinology Case Presentations 4, Eskişehir, April 27-29, 2012.

D4. Simsek E, Binay Ç, Tokar B. Homozygous p.R103X mutation in exon 2 of the 5-alpha reductase type 2 gene. Pediatric Endocrinology Case Presentations 4, Eskişehir, April 27-29, 2012.

D5. Simsek E, Binay Ç, İlhan H, İhtiyar E, Sivrikoz İ, Dündar E. Papillary thyroid cancer in a patient presented with clinical thyrotoxicosis. Pediatric Endocrinology Case Presentations 6, Çeşme, April 18-19, 2014.

D6. Simsek E, Binay Ç, Tokar B, Dündar E, Demiral M. Familial adrenocortical carcinoma. Pediatric Endocrinology Case Presentations 6, Çeşme, April 18-19, 2014.

D7. Binay Ç, Bozkurt Turhan A, Simsek E, Bor Ö, Aky M. Evaluation of coagulation status in children and adolescents with type 1 diabetes using thromboelastometry. 58th National Pediatric Congress of Turkey, Antalya, October 22-26, 2014.

D8. Darendeliler F, Yeşilkaya E, Bereket A, Baş F, Bundak R, Sarı E, Küçükemre Aydın B, Darcan Ş, Dündar B, Büyükinan M, Kara C, Mazıcıoğlu MM, Adal E, Akıncı A, Atabek ME, Demirel F, Çelik N, Özkan B, Özhan B, Orbak Z, Ersoy B, Doğan M, Ataş A, Turan S, Gökşen D, Tarım Ö, Yüksel B, Ercan O, Hatun Ş, Şimşek E, Ökten A, Abacı A, Döneray H, Özbek MN, Keskin M, Önal H, Akyürek N, Bulan K, Tepe D, Emeksiz HC, Demir K, Kızılay D, Topaloğlu AK, Eren E, Özen S, Demirbilek H, Abalı S, Akın L, Eklioğlu BS, Kaba S, Anık A, Baş S, Ünüvar T, Sağlam H, Bolu S, Özgen T, Doğan D, Çakır ED, Şen Y, Andıran N, Çizmecioğlu F, Evliyaoğlu O, Karagüzel G, Pirgon Ö, Çatlı G, Can HD, Gürbüz F, Binay Ç, Baş VN, Sağlam C, Gül D, Polat A, Açıkel C, Cinaz P. Growth curves of Turkish girls with Turner syndrome: FAVOR Turner Syndrome Study Group. National Pediatric Congress of Turkey, Antalya, November 4-8, 2014.

D9. Şimşek E, Monetegro L, Binay Ç, Demiral M, Latronika A.C. Secondary isolated FSH gene deficiency due to a new FSH gene mutation. Pediatric Endocrinology Case Presentations 7, İzmir, April 18-19, 2014.

D10. Şimşek E, Cilingir O, Binay Ç, Demiral M, Haziyeva Konul, Artan Sevilhan, Yıldız M, Çetinkaya S, Ercan O, Çayır A, Söbü E, Akın O, Yıldız M, Acar S, Gül Ü, Güven A. Screening for TP53 mutation in childhood adrenocortical carcinomas in Turkey: a multicenter study. Antalya, April 18-22, 2018.

E. Presentations Presented at International Scientific Meetings and Published in Abstract Books (Proceedings):

E1. Şimşek E, Dallar Y, Selver B, Çetinkaya S, Binay C. Which TSH response level to TRH test should be accepted for thyroid hormone replacement in Hashimoto’s thyroiditis. 50th Annual ESPE Meeting, September 25-28, 2011, Glasgow.

E2. Simsek E, Binay C, Kabukcuoğlu S, Toker B. 46,XY disorders of sexual development (DSD) presenting with normal female genital phenotype: Leydig cell hypoplasia or aplasia. 51st Annual ESPE Meeting, September 20-23, 2012, Leipzig, Germany.

E3. Simsek E, Selver B, Dallar Y, Binay C. Obesity epidemiology in children living in lower socio-economic status. 51st Annual ESPE Meeting, September 20-23, 2012, Leipzig, Germany.

E4. Simsek E, Binay C, Ceylaner S. A same homozygous mutation (R103X) in Exon 2 of 5-alpha-reductase type 2 gene (SRD5A2) presenting with different female external genital phenotype. The Endocrine Society’s 94th Annual Meeting and Expo, June 23-26, 2012, Houston, TX.

E5. Simsek E, Binay C, Tokar B, Kabukcuoğlu S. An unusual case of primary amenorrhea and short stature: ovarian resistance syndrome. 9th Joint Meeting of ESPE, September 19-22, 2013, Milan.

E6. Binay C, Simsek E, Cilingir O, Yüksel Z, Kutlay O. Prevalence of late-onset congenital adrenal hyperplasia in Turkish children presenting with premature pubarche, hirsutism, or oligomenorrhea. ESPE Meeting, September 19-22, 2013, Milan.

E7. Simsek E, Cilingir O, Binay C, Yuksel Z, Kutlay O, Kirel B, Artan S. Genotype-phenotype correlations in Turkish children with congenital adrenal hyperplasia due to 21-hydroxylase deficiency. ESPE Meeting, September 19-22, 2013, Milan.

E8. Simsek E, Binay C, Tokar B, Kabukcuoğlu S, Ustun M. Ovotesticular disorders of sexual development in a 46,XX karyotype with SRY gene expression and 46,XY karyotype with streak gonad, dysgerminoma, gonadoblastoma, and papillary tubal hyperplasia. The Endocrine Society, June 15-18, 2013, San Francisco.

E9. Binay C, Simsek E, Tekin N. Neonatal hypercalcemia associated with congenital adrenal hyperplasia. 53rd Annual Meeting of ESPE, September 18-20, 2014, Dublin.

E10. Simsek E, Binay C, Tokar B, Kabukcuoğlu S, Ustun M. Gonadoblastoma and papillary tubal hyperplasia in ovotesticular syndrome. 53rd Annual Meeting of ESPE, September 18-20, 2014, Dublin.

E11. Simsek E, Binay C, Tokar B, Dündar E, Demiral M. A novel mutation in Exon 5 of TP53 Gene in a Familial Adrenocortical Carcinoma. 53rd Annual Meeting of ESPE, September 18-20, 2014, Dublin.

E12. Simsek E, Binay C, İlhan H, İhtiyar E, Sivrikoz I, Dündar E, Akçar N. Metastatic papillary thyroid carcinoma in an autonomous hyperfunctioning thyroid nodule in an adolescent. The Endocrine Society’s Annual Meeting and Expo, June 21-24, 2014, Chicago.

E13. Binay C, Bozkurt Turhan A, Simsek E, Bor Ö, Akay M. Evaluation of coagulation profile using thromboelastography in children and adolescents with type 1 diabetes mellitus. The Endocrine Society’s Annual Meeting and Expo, June 21-24, 2014, Chicago.

E14. Simsek E, Eren M, Demiral M, Binay C, Simsek T, Tokar B. Neurofibromatosis type 1 presenting with secondary amenorrhea and wasting syndrome. The Endocrine Society’s 97th Annual Meeting and Expo, March 5-8, 2015, San Diego.

E15. Simsek E, Montelegro L.R., Binay C, Latronico A.C. Isolated follicle-stimulating hormone deficiency caused by a new missense mutation in the FSHb gene in a male adolescent with normal virilization. The Endocrine Society’s 97th Annual Meeting and Expo, March 5-8, 2015, San Diego.

E16. Binay C, Crettol L.M., Demiral M, Campos-Xavier A.B., Pereira S.D., Bonafe L, Simsek E. MMP13 mutation in a patient with rickets-like metaphyseal changes, Spahr type metaphyseal dysplasia. The Endocrine Society’s 98th Annual Meeting and Expo, April 1-4, 2016, Boston.

E17. Binay C, Ciftci Ö. A Novel COL1A2 Gene Mutation in a Turkish Family with Osteogenesis Imperfecta. 57th Annual Meeting of ESPE, September 27-29, 2018, Athens, Greece.

 

Awards

• 2018
  Oral Presentation Second Prize,
  XXII. National Pediatric Endocrinology and Diabetes Congress.

• 2015
  Poster Presentation Second Prize,
  National Pediatric Endocrinology and Diabetes Association.

• 2015
  Oral Presentation First Prize,
  Turkish National Pediatric Association.

• 2014
  Prof. Dr. Sezai Bedrettin Tümay Awards Article Competition,
  Turkish Pediatric Society.

Memberships in Scientific Organizations

• Turkish Medical Association

• Turkish Pediatric Society

• National Pediatric Association

• Pediatric Endocrinology and Diabetes Association

• ESPE (European Society of Pediatric Endocrinology)

Other Academic Activities

• Pediatric Endocrinology Case Presentations - Secretariat - 2012

• OBAT National Medical Student Congress - Session Chair and Speaker - 2014

• Children and Diabetes Sweet Children - Panelist Speaker - 2014

• Namık Kemal University Faculty of Medicine Educator Development Programs Basic and Advanced Training Skills Course - 2018

• Term 6 Coordinator - Namık Kemal University Faculty of Medicine - 2018-2019

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