B1. Keskin M, Keskin O, Temel L, Dai A, Kor Y, Güler E, Coskun MY. “Screening frequency of celiac disease and autoimmune thyroiditis in children and adolescents with type 1 diabetes mellitus in Turkey and comparision with last surveys.˝ LWPES/ESPE 8th Joint Meeting Global Care in Pediatric Endocrinology. New York, N.Y.,USA, pp.215, 2009.
B2. Kilic BD, Kor Y, Buyukcelik M, Keskin M, Balat A. “Growth Hormone Deficiency in Bartter’s Syndrome; Three cases”, The Fifteenth Congress of the International Pediatric Nephrology Association. New York, N.Y.,USA, pp. 43, 2010.
B3.Keskin M, Aygun A, Pehlivan S, Keskin O, Kor Y, Balat A, Coskun MY. “Trends in the frequency of HLA DR-DQ haplotypes among children and adolescents with type 1 diabetes mellitus in Turkey and comparison with recent surveys”, 49 th Annual Meeting of the European Society for Paediatric Endocrinology (ESPE), Prague,Czech Republic,pp.268, 2010.
B4. Keskin M, Kor Y, Yalcın A, Uygun H, Keskin O, Kor D. “Two cases with HDR syndrome (hypoparathyroidism, sensorineural deafness and renal disease)”, 50 th Annual Meeting of the European Society for Paediatric Endocrinology (ESPE), Glasgow,United Kingdom,pp.275, 2011.
B5. Keskin M,Geyikli I, Kor Y, Akan M. “Investigation of relation between melatonin and type 1 diabetes mellitus”, 51 th Annual Meeting of the European Society for Paediatric Endocrinology (ESPE), Leipzig, Germany, pp.158, 2012.
B6. Keskin M,Geyikli I, Kor Y, Akan M. “Investigation of relation between three adipokines (adiponectin, leptin, resistin) and type 1 diabetes mellitus”, 51 th Annual Meeting of the European Society for Paediatric Endocrinology (ESPE), Leipzig, Germany, pp.160, 2012.
B7. Keskin M,Yalcin AS, Oztuzcu S, Kor Y, Coskun MY “ The role of PAX-8, TTF-1 and TTF-2 gene polymorphism in children with congenital hypothyroidism due to thyroid dysgenesis”, 51 th Annual Meeting of the European Society for Paediatric Endocrinology (ESPE), Leipzig, Germany, pp.241, 2012.
B8. Kor Y, Keskin M. “ Evaluation of the diagnosis and assessment of response to treatment in patients with growth hormone ”, 51 th Annual Meeting of the European Society for Paediatric Endocrinology (ESPE), Leipzig, Germany, pp.286, 2012.
B9. Karaoglan M, Keskin M, Kor Y, Keskin O. “Distribution of the most frequent mutations and clinical charecteristic among children with 21-hydroxylase deficiency in Southeasthern of Turkey”, 9 th Joint Meeting of Paediatric Endocrinology, (ESPE), Milan, Italy, pp.370, 2013.
B10. Keskin M, Karaoglan M, Kor Y. “Clinical features of children with congenital hypothyroidism due to thyroglobulin deficiency”, 9 th Joint Meeting of Paediatric Endocrinology, (ESPE),Milan, Italy, pp.367, 2013.
B11. Karaoglan M, Keskin M, Kor Y, Keskin O, San S. “Immunogenetics and clinical characteristic of patients with the most common organ-spesific autoimmune diseases:Determinations of risk and prognostic factors” 39 th ISPAD Annual Conference, (ESPE), Gothenburg, Sweden, pp.203, 2013.
B12. Kor Y, Soker G, Kor D, Temiz F, Yüksel B. “Cushing syndrome due to multinodular adrenal hyperplasia: case report”, 9 th Joint Meeting of Paediatric Endocrinology, (ESPE),Milan, Italy, pp., 2013.
B13. Yüksel B, Gürbüz F, Kupeli BY, Kor Y, Zorludemir S, Kupeli S. “The first report of cabergoline induced immune haemolytic anaemia in an adolescent with prolactinoma”, 9 th Joint Meeting of Paediatric Endocrinology, (ESPE),Milan, Italy, pp., 2013.
B14. Uçaktürk M.E, Kor Y,Gürbüz F, Topaloğlu AK, Yüksel B. “ 5α-Steroid Reductase 2 Deficiency in a Large Family”. 53 rd Annual Meeting of the European Society for Paediatric Endocrinology (ESPE), Dublin, Ireland, 453, 2014.
B15. Kotan Gedik LD, Mengen E, Gürbüz F, Özsu E, Tunç S, Kor Y, Çakır EP, Abacı A, Demir K, Akçay T, Kırel B, Kınık TS, Özen S, Uçaktürk A, Bideci A, Durmaz E, Ünlühızarcı K, Turan I, Yüksel B, Topaloğlu AK. ˝Distribution of mutations in genes known to be associated with familial idiopathic hypogonadotropic hypogonadism in a large group.˝ 54 th Annual Meeting of the European Society for Paediatric Endocrinology (ESPE) 2015.
B16. Abacı A, Çatlı G, Kırbıyık Ö, Şahin NM, Abalı ZY, Ünal E, Şıklar Z, Mengen E, Özen S, Güran T, Kara C, Yıldız M, Eren E, Nalbantoğlu Ö, Güven A, Çayır A, Akbaş ED, Kor Y, Çürek Y, Aycan Z, Baş F, Darcan Ş, Berberoğlu M. ˝Genotype–phenotype correlation, gonadal malignancy risk, gender preference, and testosterone/dihydrotestosterone ratio in steroid 5-alpha-reductase type 2 deficiency: a multicenter study from Turkey.˝ 10.th International Meeting of Pediatric Endocrinology, USA, 2017.
B17. Kor Y. ˝Hypercalcemia Due to Six Newly Identified Inactivating Mutations in the CASR gene.˝ 57.th Annual Meeting of the European Society for Paediatric Endocrinology (ESPE), Greece, 2018
B18. Sıklar Z, Turan S, Bereket A, Abacı A, Baş F, Demir K, Güran T, Akberzade A, Böber E, Özbek MN, Kara C, Poyrazoğlu S, Aydın HM, Kardelen Aslı, Tarım ÖF, Eren E, Hatipoğlu N, Büyükinan M, Akyürek Nesibe, Çetinkaya Semra, Bayramoğlu E, Eklioğlu BS, Uçaktürk A, Abalı S, Göksen S RD, Kor Y, Ünal E, Esen I, Yıldırım R, Akın O, Cayır A, Dilek E, Kırel B, Anık A, Çatlı G, Berberoğlu M. ˝Nationwide Hypophosphatemic Rickets Study.˝ 57.th Annual Meeting of the European Society for Paediatric Endocrinology(ESPE) Greece, 2018. Oral Presentation.
B19. Kor Y. ˝Kalsiyum Algılayıcı Reseptör Inaktive Edici Mutasyon Saptanan Hiperkalsemili Hastalarımızın Klinik ve Genetik Degerlendirilmesi.˝ 4.International Academic Research Congress, Turkey, 2018. Oral Presentation.