Review
Current Management of Type 1 Diabetes in Children: Guideline-based Expert Opinions and Recommendations
Şükrü Hatun, Tuğba Gökçe, Ecem Can, et al.
Original Article
Adherence to Growth Hormone Treatment in Children During the COVID-19 Pandemic
Erdal Eren, Semra Çetinkaya, Yasemin Denkboy Öngen, et al.
Reversibility of Hyperglycemic States in Children with Obesity - Diagnostic Pitfalls in the Assessment of Glucose Metabolism in Children and Adolescents with Obesity
Anna Iwańska, Małgorzata Wójcik, Ewa Szczudlik, et al.
Estrogen Receptor 1 Gene Polymorphism and its Association with Idiopathic Short Stature in a North Indian Population
Ravi Shankar Patel, Roshan Daniel, Chitra Bhardwaj, et al.
Comprehensive Insights Into Pediatric Craniopharyngioma: Endocrine and Metabolic Profiles, Treatment Challenges, and Long-term Outcomes from a Multicenter Study
Zeynep Şıklar, Elif Özsu, Sirmen Kızılcan Çetin, et al.
Clinical and Laboratory Characteristics of MODY Cases, Genetic Mutation Spectrum and Phenotype-genotype Relationship
Elif Özsu, Semra Çetinkaya, Semih Bolu, et al.
Triglyceride Glucose Index is Associated with Ultrasonographic Fatty Liver Indicator in Children and Adolescents with Non-alcoholic Fatty Liver Disease
Bitgyeol Kim, Hye Young Jin, Jong Seo Yoon, et al.
Differentiated Thyroid Cancer in Children and Adolescents: 12-year Experience in a Single Center
Francisca Marques Puga, Laura Correia, Inês Vieira, et al.
Brief Report
Vitamin D Status in an Italian Pediatric Cohort: Is There a Role for Tobacco Smoking Exposure?
Maria Grazia Clemente, Dario Argiolas, Stefania Bassu, et al.
Case Report
Mitotically Active Follicular Nodule in Early Childhood: A Case Report with a Novel Mutation in the Thyroglobulin Gene
Sirmen Kızılcan Çetin, Zehra Aycan, Zeynep Şıklar, et al.
A New Variant of the IER3IP1 Gene: The First Case of Microcephaly, Epilepsy, and Diabetes Syndrome 1 from Turkey
Elif Söbü, Gül Demet Kaya Özçora, Elif Yılmaz Güleç, et al.
Painless Footdrop in a Child with Newly Diagnosed Type 1 Diabetes Mellitus: Case Report
Maryam Jafari, Ahmedyar Hasan, Jessie Joseph, et al.
Elemental Milk Formula as a Possible Cause of Hypophosphatemic Rickets in Wiedemann-Steiner Syndrome
Fahad Al-Juraibah, Maali Melha, Azam Alromaih, et al.
Mild Aromatic L-Amino Acid Decarboxylase Deficiency Causing Hypoketotic Hypoglycemia in a 4-year-old Girl
Merve Yoldaş Çelik, Ebru Canda, Havva Yazıcı, et al.
Sepsis-induced Pancytopenia in an Adolescent Girl with Thyroid Storm: A Case Report
Qing Zhou, Li-Yong Zhang, Qing-Xian Fu, et al.
Clinical Presentation and Genetic Analysis of Neonatal 11β-Hydroxylase Deficiency Induced by a Chimeric CYP11B2/CYP11B1 Gene
Wenjuan Cai, Dan Yu, Jian Gao, et al.
