Review
Syndromic Disorders Caused by Disturbed Human Imprinting
Diana Carli, Evelise Riberi, Giovanni Battista Ferrero, et al.
Current Diagnosis, Treatment and Clinical Challenges in the Management of Lipodystrophy Syndromes in Children and Young People
Samim Özen, Barış Akıncı, Elif A. Oral
Can Nesfatin-1 Predict Hypertension in Obese Children?
Hatice Güneş, Filiz Alkan Baylan, Hakan Güneş, et al.
Treatment with Depot Leuprolide Acetate in Girls with Idiopathic Precocious Puberty: What Parameter should be Used in Deciding on the Initial Dose?
Doğuş Vurallı, Ayfer Alikaşifoğlu, İrem İyigün, et al.
The Significance of Thiol/Disulfide Homeostasis and Ischemia-modified Albumin Levels in Assessing Oxidative Stress in Obese Children and Adolescents
Eda Mengen, Seyit Ahmet Uçaktürk, Pınar Kocaay, et al.
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 Yayıcı Köken, Cengiz Kara, Gülay Can Yılmaz, et al.
Effects of 5-Hydroxymethylfurfural on Pubertal Development of Female Wistar Rats
Selin Elmaoğulları, Elçin Kadan, Elvan Anadol, et al.
Assessment of Bisphenol A Levels in Preschool Children: Results of a Human Biomonitoring Study in Ankara, Turkey
İsmet Çok, Özlem Toprak İkidağ, Dilek Battal, et al.
Evaluation of Turner Syndrome Knowledge among Physicians and Parents
Berna Eroğlu Filibeli, Nesrin Havare, Huriye Erbak Yılmaz, et al.
Hypophosphatasia: A Novel Mutation Associated with an Atypical Newborn Presentation
Roger Esmel-Vilomara, Susana Hernández, Ariadna Campos-Martorel, et al.
Aromatase Deficiency in Two Siblings with 46,XX Karyotype Raised as Different Genders: A Novel Mutation (p.R115X) in the CYP19A1 Gene
Samim Özen, Tahir Atik, Özlem Korkmaz, et al.
A Neurofibromatosis Noonan Syndrome Patient Presenting with Abnormal External Genitalia
Esra Işık, Hüseyin Onay, Tahir Atik, et al.
An Unusual Presentation of Carney Complex
Aydilek Dağdeviren Çakır, Hande Turan, Tiraje Celkan, et al.
An Iranian Patient with Maroteaux Type Acromesomelic Dysplasia, Showing no Involvement of Distal Lower Limbs
Hossein Moravej, Mozhagn Moghtaderi, Sara Mostafavi
