| Syndromic Disorders Caused by Disturbed Human Imprinting | Diana CARLI,Evelise RIBERI,Giovanni Battista FERRERO,Alessandro MUSSA | 1–16 |
| Approach to Abnormal Uterine Bleeding in Adolescents | Cenk YAŞA,Funda GÜNGÖR UĞURLUCAN | 1–6 |
| Dysmenorrhea, Endometriosis and Chronic Pelvic Pain in Adolescents | Aalia SACHEDİNA,Nicole TODD | 7–17 |
| Current Diagnosis, Treatment and Clinical Challenges in the Management of Lipodystrophy Syndromes in Children and Young People | Samim ÖZEN,Barış AKINCI,Elif A. ORAL | 17–28 |
| Where Have the Periods Gone? The Evaluation and Management of Functional Hypothalamic Amenorrhea | Marie Eve Sophie GİBSON,Nathalie FLEMİNG,Caroline ZUİJDWİJK,Tania DUMONT | 18–27 |
| Contraception for Adolescents | Nicole TODD,Amanda BLACK | 28–40 |
| Can Nesfatin-1 Predict Hypertension in Obese Children? | Hatice GÜNEŞ,Filiz ALKAN BAYLAN,Hakan GÜNEŞ,Fatih TEMİZ | 29–36 |
| Treatment with Depot Leuprolide Acetate in Girls with Idiopathic Precocious Puberty: What Parameter should be Used in Deciding on the Initial Dose? | Doğuş VURALLI,Ayfer ALLİKAŞİFOĞLU,İrem İYİGÜN,Dicle CANORUÇ,Alev OZON,E. Nazlı GÖNÇ,Nurgün KANDEMİR | 37–44 |
| Management of Menstrual and Gynecologic Concerns in Girls with Special Needs | Özlem DURAL,İnci Sema TAŞ,Süleyman Engin AKHAN | 41–45 |
| The Significance of Thiol/Disulfide Homeostasis and Ischemiamodified Albumin Levels in Assessing Oxidative Stress in Obese Children and Adolescents | Eda MENGEN,Seyit Ahmet UÇAKTÜRK,Pınar KOCAAY,Özlem KAYMAZ,Salim NEŞELİOĞLU,Özcan EREL | 45–54 |
| Hormone Replacement Therapy in a Patient with Hypogonadism and Coexisting Medical Conditions | Özlem DURAL,Şükran POYRAZOĞLU | 46–49 |
| Conservative Management of Vaginal Hypoplasia | Özlem DURAL,Şükran POYRAZOĞLU | 50–52 |
| Prevalence of Obesity and Metabolic Syndrome in Children with Type 1 Diabetes: A Comparative Assessment Based on Criteria Established by the International Diabetes Federation, World Health Organisation and National Cholesterol Education Program | Özlem KÖKEN,Cengiz KARA,Gülay Can YILMAZ,Hasan Murat AYDIN | 55–62 |
| Macular Variability in Children and Adolescents with Metabolic Syndrome: A Cross-sectional Study Examining the Associations with Anthropometric Measurements, Metabolic Parameters and Inflammatory Markers | A. Hakan ÖZTÜRK,Bediz ÖZEN,Gönül ÇATLI,Bumin N. DÜNDAR | 63–70 |
| Growth and Adult Height during Human Growth Hormone Treatment in Chinese Children with Multiple Pituitary Hormone Deficiency Caused by Pituitary Stalk Interruption Syndrome: A Single Centre Study | Fengxue WANG,Jinyan HAN,Zengmin WANG,Xiaohong SHANG,Guimei LI | 71–78 |
| Effects of 5-Hydroxymethylfurfural on Pubertal Development of Female Wistar Rats | Selin ELMAOĞULLARI,Elçin KADAN,Elvan ANADOL,Ayris GÖKÇEOĞLU,Semra ÇETİNKAYA,Gül Fatma YARIM,Seyit Ahmet UÇAKTÜRK,Zehra AYCAN | 79–85 |
| Assessment of Bisphenol A Levels in Preschool Children: Results of a Human Biomonitoring Study in Ankara, Turkey | İsmet ÇOK,Özlem TOPRAK İKİDAĞ,Dilek BATTAL,Ayça AKTAŞ ŞÜKÜROĞLU | 86–94 |
| Evaluation of Turner Syndrome Knowledge among Physicians and Parents | Berna FİLİBELİ,Nesrin HAVARE,Huriye ERBAK YILMAZ,Jülide Gülizar YILDIRIM,Gönül ÇATLI,Bumin N. DÜNDAR | 95–103 |
| Hypophosphatasia: A Novel Mutation Associated with an Atypical Newborn Presentation | Roger ESMEL-VILOMARA,Susana HERNANDEZ,Ariadna CAMPOS-MARTORE,Eva GONZALES-ROCA,Diego YESTE,F lix CASTILLO | 104–108 |
| Aromatase Deficiency in Two Siblings with 46,XX Karyotype Raised as Different Genders: A Novel Mutation (p.R115X) in the CYP19A1 Gene | Samim ÖZEN,TAHİR ATİK,Özlem Korkmaz DİLMEN,Hüseyin ONAY,Damla GÖKŞEN,F. Ferda ÖZKINAY,Muhsin Özgür ÇOĞULU,Şükran DARCAN | 109–112 |
| A Neurofibromatosis Noonan Syndrome Patient Presenting with Abnormal External Genitalia | Esra IŞIK,Hüseyin ONAY,Tahir ATİK,Aslı Ece SOLMAZ,Samim ÖZEN,Muhsin Özgür ÇOĞULU,Şükran DARCAN,F. Ferda ÖZKINAY | 113–116 |
| An Unusual Presentation of Carney Complex | Aydilek DAĞDEVİREN ÇAKIR,Hande TURAN,Tülin Tiraje CELKAN,Nil ÇOMUNOĞLU,Oya ERCAN,Olcay EVLİYAOĞLU | 117–121 |
| An Iranian Patient with Maroteaux Type Acromesomelic Dysplasia, Showing no Involvement of Distal Lower Limbs | Hossein MORAVEJ,Mozhgan MOGHTADERI,Sara MOSTAFAVI | 122–123 |