Other
Achieving Optimal Short- and Long-term Responses to Paediatric Growth Hormone Therapy
Jan M. Wit, Asma Deeb, Bassam Bin-Abbas, et al.
Novel Mutations in Obesity-related Genes in Turkish Children with Non-syndromic Early Onset Severe Obesity: A Multicentre Study
Ayşehan Akıncı, Doğa Türkkahraman, İbrahim Tekedereli, et al.
Glucose Metabolism Evaluated by Glycated Hemoglobin and Insulin Sensitivity Indices in Children Treated with Recombinant Human Growth Hormone
Maria Chiara Pellegrin, Daria Michelon, Elena Faleschini, et al.
Impact of Socioeconomic Characteristics on Metabolic Control in Children with Type 1 Diabetes in a Developing Country
Abeer Alassaf, Rasha Odeh, Lubna Gharaibeh, et al.
Serum Neuron-specific Enolase and S100 Calcium-binding Protein B in Pediatric Diabetic Ketoacidosis
Hatem Hamed Elshorbagy, Naglaa Fathy Barseem, Akram Elshafey Elsadek, et al.
Clinical and Biochemical Phenotype of Adolescent Males with Gynecomastia
Miłosz Lorek, Dominika Tobolska-Lorek, Barbara Kalina-Faska, et al.
Liver Biochemical Abnormalities in Adolescent Patients with Turner Syndrome
Małgorzata Wójcik, Anna Ruszała, Dominika Januś, et al.
Clinical Management and Gene Mutation Analysis of Children with Congenital Hyperinsulinism in South China
Aijing Xu, Jing Cheng, Huiying Sheng, et al.
Subclinical Myocardial Dysfunction Demonstrated by Speckle Tracking Echocardiography in Children with Euthyroid Hashimoto’s Thyroiditis
Emine Azak, Seyit Ahmet Uçaktürk, İbrahim İlker Çetin, et al.
A Novel Nonsense Mutation of PHF6 in a Female with Extended Phenotypes of Borjeson-Forssman-Lehmann Syndrome
Xia Zhang, Yanjie Fan, Xiaomin Liu, et al.
Isolated Growth Hormone Deficiency Type 2 due to a novel GH1 Mutation: A Case Report
Ahmad Kautsar, Jan M. Wit, Aman Pulungan
A Novel Homozygous Mutation of the Acid-Labile Subunit (IGFALS) Gene in a Male Adolescent
Şükran Poyrazoğlu, Vivian Hwa, Firdevs Baş, et al.
A Case of Autosomal Dominant Osteopetrosis Type 2 with a CLCN7 Gene Mutation
Sol Kang, Young Kyung Kang, Jun Ah Lee, et al.
Three Siblings with Idiopathic Hypogonadotropic Hypogonadism in a Nonconsanguineous Family: A Novel KISS1R/GPR54 Loss-of-Function Mutation
Özlem Nalbantoğlu, Gülçin Arslan, Özge Köprülü, et al.
