| Clinicopathological Characteristics of Papillary Thyroid Cancer in Children with Emphasis on Pubertal Status and Association with BRAFV600E Mutation | ŞÜKRAN POYRAZOĞLU,RÜVEYDE BUNDAK,FİRDEVS BAŞ,Gülçin YEĞEN,YASEMİN ŞANLI,FATMA FEYZA DARENDELİLER | 185–193 |
| Congenital Hyperinsulinism in China: A Review of Chinese Literature Over the Past 15 Years | Wei-Yan WANG,Yi SUN,Wen-Ting ZHAO,Tai WU,Liang WANG,Tian-Ming YUAN,Hui-Min YU | 194–201 |
| The Relationship Between Glycemic Variability and Inflammatory Markers in Obese Children with Insulin Resistance and Metabolic Syndrome | Abdurrahman KAYA,Cemil KOÇYİĞİT,GÖNÜL ÇATLI,Elif Büşra ÖZKAN,BUMİN NURİ DÜNDAR | 202–207 |
| Treatment of Pre-pubertal Patients with Growth Hormone Deficiency: Patterns in Growth Hormone Dosage and Insulin-like Growth Factor-I Z-scores | Megan OBERLE,Adda GRİMBERG,Vaneeta BAMBA | 208–215 |
| Melanocortin-4 Receptor Gene Mutations in a Group of Turkish Obese Children and Adolescents | Selma TUNÇ,Korcan DEMİR,Fatma Ajlan TÜKÜN,Cihan TOPAL,Filiz HAZAN,Burcu SAĞLAM,Özlem NALBANTOĞLU,Melek YILDIZ,Behzat ÖZKAN | 216–221 |
| Management of Childhood Thyroid Nodules: Surgical and Endocrinological Findings in a Large Group of Cases | Emre DİVARCI,Ülgen ÇELTİK,ÜLKÜM ZAFER DÖKÜMCÜ,MUSTAFA ORKAN ERGÜN,MEHMET GEYLANİ ÖZOK,SAMİM ÖZEN,RUHSAR DAMLA GÖKŞEN ŞİMŞEK,ŞÜKRAN DARCAN,Nazan ÇETİNGÜL,Aylin ORAL,YEŞİM ERTAN,Bengü DEMİRAĞ,AHMET ÇELİK | 222–228 |
| Clinical and Genetic Findings of Turkish Hypophosphatasia Cases | HALİL SAĞLAM,ŞAHİN ERDÖL,Sevil DORUM | 229–236 |
| The Relationship of Disordered Eating Attitudes with Stress Level, Bone Turnover Markers, and Bone Mineral Density in Obese Adolescents | Aslı GÜNEŞ OKBAY,Müjgan ALİKAŞİFOĞLU,Ezgi DEMİRDÖĞEN ŞEN,ETHEM ERGİNÖZ,Türkay DEMİR,MİNE KUCUR,OYA ERCAN | 237–245 |
| Phenotype Heterogeneity in Glucokinase-Maturity-Onset Diabetes of the Young (GCK-MODY) Patients | Anna WEDRYCHOWİCL,Ewa TOBÓR,Malgorzata STELMACH,Jerzy STARZYK,Barbara SABAL,Anna RAMS,Magdalena WİLK,Ewa ZİÓLKOWSKA-LEDWİTH,Katarzyna WZOREK | 246–252 |
| The Relationship Between Perceived Family Climate and Glycemic Control in Type 1 Diabetes Mellitus Adolescent Patients | ŞAFAK ERAY,HALİT NECMİ UÇAR,Fatma ÇETİNKAYA,ERDAL EREN,AYŞE PINAR VURAL | 253–259 |
| An ABCC8 Nonsense Mutation Causing Neonatal Diabetes Through Altered Transcript Expression | Sarah E FLANAGAN,Vu Chí DUNG,Jayne A L HOUGHTON,Elisa De FRANCO,Can Thi Bich NGOC,Annet DAMHUİS,Frances M ASHCROFT,Lorna W HARRİES,Sian ELLARD | 260–264 |
| Pituitary Adenoma Apoplexy in an Adolescent: A Case Report and Review of the Literature | Hero ZİJLKER,Sebastian SCHAGEN,Jan Maarten WİT,Nienke BİERMASZ,Wouter van FURTH,Wilma OOSTDİJK | 265–273 |
| Pancreatic Agenesis due to Compound Heterozygosity for a Novel Enhancer and Truncating Mutation in the PTF1A Gene | Monica GABBAY,Sian ELLARD,Elisa De FRANCO,Regina S. MOİSÉS | 274–277 |
| Congenital Central Hypothyroidism Caused by a Novel Thyroid- Stimulating Hormone-Beta Subunit Gene Mutation in Two Siblings | BAYRAM ÖZHAN,Özlem ANLAŞ BOZ,Bilge SARIKEPE,BURCU ALBUZ,Nur GÜNDÜZ SEMERCİ | 278–282 |
| Long-Term Follow-up of a Case with Proprotein Convertase 1/3 Deficiency: Transient Diabetes Mellitus with Intervening Diabetic Ketoacidosis During Growth Hormone Therapy | E. Nazlı GÖNÇ,ZEYNEP ALEV ÖZÖN,AYFER ALİKAŞİFOĞLU,Nurgün KANDEMİR | 283–287 |
| Tolvaptan Treatment in Children with Chronic Hyponatremia due to Inappropriate Antidiuretic Hormone Secretion: A Report of Three Cases | Gerdi TULİ,Daniele TESSARİS,Silvia EİNAUDİ,Luisa De SANCTİS,Patrizia MATARAZZO | 288–292 |