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Journal of Clinical Research in Pediatric Endocrinology|January 19, 2016
Gonadoblastoma with Dysgerminoma in a Phenotypically Turner-Like Girl with 45,X/46,XY KaryotypeÖzge Yüce, Esra Döğer, Nurullah Çelik, et al.Journal of Clinical Research in Pediatric Endocrinology|January 14, 2016
Delayed Adrenarche may be an Additional Feature of Immunoglobulin Super Family Member 1 Deficiency SyndromeSeverine Van Hulle, Margarita Craen, Bert Callewaert, et al.Journal of Clinical Research in Pediatric Endocrinology|January 14, 2016
Relationship between Neck Circumference and Non-Alcoholic Fatty Liver Disease in Childhood ObesityNihal Hatipoğlu, Serap Doğan, M Mümtaz Mazıcıoğlu, et al.Journal of Clinical Research in Pediatric Endocrinology|January 14, 2016
A Novel c.554+5C>T Mutation in the DUOXA2 Gene Combined with p.R885Q Mutation in the DUOX2 Gene Causing Congenital HypothyroidismXiao Zheng, Shao Gang Ma, Ya Li Qiu, et al.Journal of Clinical Research in Pediatric Endocrinology|January 14, 2016
Evaluation of Iodine Deficiency in Children with Attention Deficit/Hyperactivity DisorderSaliha Kanık Yüksek, Zehra Aycan, Özgür ÖnerJournal of Clinical Research in Pediatric Endocrinology|January 14, 2016
Prediabetes and Cardiovascular Parameters in Obese Children and AdolescentsBeray Selver Eklioğlu, Mehmet Emre Atabek, Nesibe Akyürek, et al.Journal of Clinical Research in Pediatric Endocrinology|January 14, 2016
A Novel Homozygous Mutation in the Transient Receptor Potential Melastatin 6 Gene: A Case ReportAyça Altıncık, Karl Peter Schlingmann, Mahya Sultan TosunJournal of Clinical Research in Pediatric Endocrinology|January 14, 2016
Effects of Thyroid Autoimmunity on Early Atherosclerosis in Euthyroid Girls with Hashimoto's ThyroiditisPınar İşgüven, Yasemin Gündüz, Mukaddes KılıçJournal of Clinical Research in Pediatric Endocrinology|May 17, 2016
A Novel Homozygous Mutation in the KCNJ11 Gene of a Neonate with Congenital Hyperinsulinism and Successful Management with SirolimusSevim Ünal, Deniz Gönülal, Ahmet Uçaktürk, et al.Journal of Clinical Research in Pediatric Endocrinology|April 19, 2016
A Novel Null Mutation in P450 Aromatase Gene (CYP19A1) Associated with Development of Hypoplastic Ovaries in HumansSema Akçurin, Doğa Türkkahraman, Woo Young Kim, et al.Pageof 112