Review
Specific Functions of Melanocortin 3 Receptor (MC3R)
Tulin Yanik, Seyda Tugce Durhan
Factors Affecting Thyroid Elastography in Healthy Children and Patients with Hashimoto’s Thyroiditis
Serkan Bilge Koca, Turgut Seber
Endocrine Abnormalities and Growth Characterization in Colombian Pediatric Patients with 22q11 Deletion Syndrome
Juan Lasprilla-Tovar, Nora Alejandra Zuluaga, Carolina Forero, et al.
Anomalies in Human Sex Determination: Usefulness of a Combined Cytogenetic Approach to Characterize an Additional Case with Xp Functional Disomy Associated with 46,XY Gonadal Dysgenesis
Khouloud Rjiba, Wafa Slimani, Meriem Gaddas, et al.
Clinical Utility and Outcome Prediction of Early ZnT8-IgG Testing and Titer in Type 1 Diabetes
Amanda R. Dahl, Sarah Jenkins M., Sean J. Pittock, et al.
Comparison of Commonly Used Methods to Predict the Final Height in Constitutional Tall Stature
Alma Kamar Matias, Evgenia Muginshtein-Simkovitch, Gilad Twig, et al.
Frequency, Clinical Characteristics and Predictors of Ketoacidosis at Diagnosis of Type One Diabetes Mellitus in Children and Adolescents from Jordan
Rasha Odeh, Lobna Gharaibeh, Amirah Daher, et al.
The Relationship Between Premature Adrenarche and Platelet Aggregation
Ahmet Bolat, Cengiz Zeybek, Orhan Gürsel, et al.
Factors Associated with Low Bone Mineral Density at the Time of Diagnosis in Children with Celiac Disease
Emine Çamtosun, Fatma İlknur Varol, Şükrü Güngör, et al.
Increased Carotid Intima-media Thickness and Its Association with Carbohydrate Metabolism and Adipocytokines in Children Treated with Recombinant Growth Hormone
Seha Saygılı, Mehmet Kocaağa, Gamze Kaya, et al.
Weight Loss During Topiramate Treatment in a Severely Obese Adolescent with Congenital Adrenal Hyperplasia and Migraine
Amy Seagroves, Heather M. Ross, Alaina P. Vidmar, et al.
Rare Coexistence of Congenital Adrenal Hyperplasia due to 21-Hydroxylase Deficiency and Turner Syndrome: A Case Report and Brief Literature Review
Isabel Inácio, Joana Serra-Caetano, Rita Cardoso, et al.
Expanding the Phenotype of TRMT10A Mutations: Case Report and a Review of the Existing Cases
Zeynep Şıklar, Tuğba Kontbay, Kevin Colclough, et al.
Compound Heterozygous Variants in FAM111A Cause Autosomal Recessive Kenny-Caffey Syndrome Type 2
Erdal Eren, Havva Tezcan Ünlü, Serdar Ceylaner, et al.
Maltodextrin May Be a Promising Treatment Modality After Neartotal Pancreatectomy in Infants Younger Than Six Months with Persistent Hyperinsulinism: A Case Report
Yasemin Denkboy Öngen, Erdal Eren, Halil Sağlam
