Review
A Current Perspective on Delayed Puberty and Its Management
Ayhan Abacı, Özge Besci
Current Diagnostic Approaches in the Genetic Diagnosis of Disorders of Sex Development
Deniz Özalp Kızılay, Samim Özen
Predictors and Trends of Diabetic Ketoacidosis at Diagnosis of Type 1 Diabetes Mellitus in Malaysian Children
Meenal Mavinkurve, Nurul Hanis Ramzi, Muhammad Yazid Bin Jalaludin, et al.
The Relationship Between Sleep Quality, Sleep Duration, Social Jet Lag and Obesity in Adolescents
Funda Yıldız, Melike Zeynep Tuğrul Aksakal, Raif Yıldız, et al.
Electrocardiographic Findings in Children Treated with Leuprolide Acetate for Precocious Puberty: Does it Cause Prolonged QT?
Esma Ebru Altun, Ayşe Yaşar, Fatma Dursun, et al.
Molecular Genetic Diagnosis with Targeted Next Generation Sequencing in a Cohort of Turkish Osteogenesis Imperfecta Patients and their Genotype-phenotype Correlation
Samim Özen, Damla Gökşen, Ferda Evin, et al.
Treatment of Severe Hyperglycemia in Extremely Preterm Infants Using Continuous Subcutaneous Insulin Therapy
Merle Böettger, Tony Zhou, Jennifer Knopp, et al.
Whole Exome Sequencing Revealed Paternal Inheritance of Obesity-related Genetic Variants in a Family with an Exclusively Breastfed Infant
Hazal Banu Olgun Çelebioğlu, Ayşe Pınar Öztürk, Şükran Poyrazoğlu, et al.
Frequency of Delayed Puberty in Boys with Contemporary Management of Duchenne Muscular Dystrophy
Sarah McCarrison, Melissa Denker, Jennifer Dunne, et al.
Assessment of the Admission and Follow-up Characteristics of Children Diagnosed with Secondary Osteoporosis
Emine Kübra Şen, Merih Berberoğlu, Gizem Şenyazar, et al.
Long-term Follow-up of a Late Diagnosed Patient with Temple Syndrome
Nikolinka Yordanova, Violeta Iotova, Deborah J. G. Mackay, et al.
Long-term Growth Hormone Therapy in a Patient with IGF1R Deletion Accompanied by Delayed Puberty and Central Hypothyroidism
Nur Berna Çelik, Monique Losekoot, Emregül Işık, et al.
A Boy with Reset Osmostat Who Developed Chronic Hyponatremia due to Hypothalamic Injury Caused By a Giant Arachnoid Cyst
Junko Naganuma, Satomi Koyama, Yoshiyuki Watabe, et al.
Seminoma in 46, XY Gonadal Dysgenesis: Rare Presentation and Review of the Literature
Maamoun Adra, Hayato Nakanishi, Eleni Papachristodoulou, et al.
Novel OBSL1 Variant in a Chinese Patient with 3M Syndrome: The c.458dupG Mutation May Be a Potential Hotspot Mutation in the Chinese Population
Yurong Piao, Rongmin Li, Yingjie Wang, et al.
Clinical and Genetic Characteristics and Outcome in Patients with Neonatal Diabetes Mellitus from a Low Middle-income Country
Ishara Minuri Kumarasiri, Thabitha Jebaseeli Hoole, Manimel Wadu Akila Nimanthi, et al.
In Response to: “Involvement of the Endocrine System is Common in Mitochondrial Disorders and Requires Long-term Comprehensive Investigations”
Esra Deniz Papatya Çakır, Melike Ersoy, Nihan Çakır Biçer, et al.
