| Novel Modulators of the Growth Hormone - Insulin-Like Growth Factor Axis: Pregnancy-Associated Plasma Protein-A2 and Stanniocalcin-2 | Masanobu FUJİMOTO,Vivian HWA,Andrew DAUBER | 1–8 |
| Latest Insights on the Etiology and Management of Primary Adrenal Insufficiency in Children | Tülay GÜRAN | 9–22 |
| The Rationale for Growth Hormone Therapy in Children with Short Stature | Annalisa DEODATİ,Stefano CİANFARANİ | 23–32 |
| A Critical Appraisal of the Effect of Gonadotropin-Releasing Hormon Analog Treatment on Adult Height of Girls with Central Precocious Puberty | Abdullah BEREKET | 33–48 |
| Insulin Resistance, Prediabetes, Metabolic Syndrome: What Should Every Pediatrician Know? | Ahmad IGHBARİYA,Ram WEİSS | 49–57 |
| Current Nomenclature of Pseudohypoparathyroidism: Inactivating Parathyroid Hormone/Parathyroid Hormone-Related Protein Signaling Disorder | Serap TURAN | 58–68 |
| Congenital Hyperinsulinism: Diagnosis and Treatment Update | Hüseyin DEMİRBİLEK,Khalid HUSSAIN | 69–87 |
| Genetic Causes of Rickets | Sezer ACAR,KORCAN DEMİR,Yufei SHİ | 88–105 |
| Hypogonadotropic Hypogonadism due to Novel FGFR1 Mutations | GAMZE AKKUŞ,LEMAN DAMLA KOTAN GEDİK,Erdem DURMAZ,Eda MENGEN,İHSAN TURAN,Ayça ULUBAY,FATİH GÜRBÜZ,BİLGİN YÜKSEL,BEKİR TAMER TETİKER,A. Kemal TOPALOĞLU | 95–100 |
| Basal Serum Neurokinin B Levels in Differentiating Idiopathic Central Precocious Puberty from Premature Thelarche | Mesut PARLAK,DOĞA TÜRKKAHRAMAN,Hamit Yaşar ELLİDAĞ,Gamze ÇELMELİ,Ayşe Eda PARLAK,Necat YILMAZ | 101–105 |
| Congenital Hypothyroidism and Bone Remodeling Cycle | NAZMİ MUTLU KARAKAŞ,Sibel Tulgar KINIK,Beril ÖZDEMİR,Nursel MURATOĞLU ŞAHİN,M. Agah TEKİNDAL,Ayşegül HABERAL | 106–110 |
| Sex Assignment in Conditions Affecting Sex Development | Renata MARKOSYAN,S Faisal AHMED | 106–112 |
| Association between Obesity and Parental Weight Status in Children and Adolescents | Maryam BAHREYNİAN,Mostafa QORBANİ,Bita Moradi KHANİABADİ,Mohammad Esmaeil MOTLAGH,Omid SAFARI,Hamid ASAYESH,Roya KELİSHADİ | 111–117 |
| Update on the Genetics of Idiopathic Hypogonadotropic Hypogonadism | A. Kemal TOPALOĞLU | 113–122 |
| Heart-Type Fatty Acid Binding Protein Level as a Tool in Identification of Early Cardiac Effects of Diabetic Ketoacidosis | Fatma Hilal YILMAZ,Sevil YUCA ARI,HÜSAMETTİN VATANSEV,Emine Ayca CİMBEK,Yaşar ŞEN,İsa YILMAZ,Fikret AKYÜREK,DERYA ARSLAN,Derya ÇİMEN,ALAADDİN YORULMAZ | 118–123 |
| Serum Irisin and Oxytocin Levels as Predictors of Metabolic Parameters in Obese Children | Çiğdem BİNAY,CEM PAKETÇİ,SAVAŞ GÜZEL,Nedim SAMANCI | 124–131 |
| Higher-Than-Conventional Subcutaneous Regular Insulin Doses in Diabetic Ketoacidosis in Children and Adolescents | Özlem BAĞ,Selma TUNÇ,Özlem NALBANTOĞLU,Çiğdem ECEVİT,Aysel ÖZTÜRK,BEHZAT ÖZKAN,Korcan DEMİR | 132–137 |
| Gene Polymorphisms of Glutathione S-Transferase T1/M1 in Egyptian Children and Adolescents with Type 1 Diabetes Mellitus | Naglaa BARSEEM,Mona ELSAMALEHY | 138–143 |
| Association of Subclinical Hypothyroidism with Dyslipidemia and Increased Carotid Intima-Media Thickness in Children | Edip ÜNAL,ALPER AKIN,Ruken YILDIRIM,Vasfiye DEMİR,İsmail YILDIZ,YUSUF KENAN HASPOLAT | 144–149 |
| Can Stoss Therapy Be Used in Children with Vitamin D Deficiency or Insufficiency without Rickets? | Cemil KOÇYİĞİT,GÖNÜL ÇATLI,Gülberat İNCE,Elif ÖZKAN BÜŞRA,BUMİN NURİ DÜNDAR | 150–155 |
| Menarcheal Age and Risk of Type 2 Diabetes: A Community-Based Cohort Study | Maryam FARAHMAND,Fahimeh Ramezani TEHRANİ,Marzieh Rostami DOVOM,Fereidoun AZİZİ | 156–162 |
| Delayed Diagnosis of a 17-Hydroxylase/17,20-Lyase Deficient Patient Presenting as a 46,XY Female: A Low Normal Potassium Level Can Be an Alerting Diagnostic Sign | EMİNE ÇAMTOSUN,ZEYNEP ŞIKLAR,Serdar CEYLANER,Pınar KOCAAY,MERİH BERBEROĞLU | 163–167 |
| Response to Anastrozole Treatment in a Case with Peutz-Jeghers Syndrome and a Large Cell Calcifying Sertoli Cell Tumor | Merve YEKEDÜZ KOÇ,ZEYNEP ŞIKLAR,BERK BURGU,Zarife KULOĞLU,Pınar KOCAAY,EMİNE ÇAMTOSUN,Mehmet İSAKOCA,Aydan KANSU,YAKUP TARKAN SOYGÜR,MERİH BERBEROĞLU | 168–171 |
| The Effectiveness of Cinacalcet as an Adjunctive Therapy for Hereditary 1,25 Dihydroxyvitamin D-Resistant Rickets | Ayşehan AKINCI,İsmail DÜNDAR,Meltem KIVILCIM | 172–178 |
| Persistent Müllerian Duct Syndrome with Transverse Testicular Ectopia: A Novel Anti-Müllerian Hormone Receptor Mutation | Özlem KORKMAZ,Samim ÖZEN,Nurhan ÖZCAN,Petek BAYINDIR,SAİT ŞEN,HÜSEYİN ONAY,Damla GÖKŞEN,Ali AVANOĞLU,FERİŞTAH FERDA ÖZKINAY,Şükran DARCAN | 179–181 |
| A Comprehensive Online Calculator for Pediatric Endocrinologists: ÇEDD Çözüm/TPEDS Metrics | KORCAN DEMİR,SAMİM ÖZEN,Ergun KONAKÇI,HASAN MURAT AYDIN,FATMA FEYZA DARENDELİLER | 182–184 |