Original Article
PROKR2 Mutations in Patients with Short Stature Who Have Isolated Growth Hormone Deficiency and Multiple Pituitary Hormone Deficiency
Aslı Derya Kardelen, Adam Najaflı, Firdevs Baş, et al.
Relative Frequency of Islet Autoimmunity in Children and Adolescents with Autoimmune Thyroid Disease
Natasa Rojnic Putarek, Nevena Krnic, Jadranka Knezevic-Cuca, et al.
The Incidence Trend of Type 1 Diabetes among Children and Adolescents 0-14 Years of Age in the West, South, and Tripoli Regions of Libya (2009-2018)
Rowida M. Khashebi, Christopher C. Patterson, Mostafa S. Shebani
Effects of Blue Light on Puberty and Ovary in Female Rats
Aylin Kılınç Uğurlu, Aysun Bideci, Mürşide Ayşe Demirel, et al.
Peak Serum Cortisol Cutoffs to Diagnose Adrenal Insufficiency Across Different Cortisol Assays in Children
Samuel Cortez, Ana Maria Arbeláez, Michael Wallendorf, et al.
Continuous Glucose Monitoring in Children and Adolescents with Congenital Adrenal Hyperplasia
Ilja Dubinski, Susanne Bechtold-Dalla Pozza, Belana Debor, et al.
Comparison of Optical Coherence Tomography Angiography Findings between Healthy Children and Children with Type 1 Diabetes Mellitus and Autoimmune Thyroiditis
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Pulse Wave Analysis in Obese Children with and without Metabolic Syndrome
Cemaliye Başaran, Gökçen Erfidan, Özgür Özdemir-Şimşek, et al.
Screening for Anxiety and Depression in Children with Congenital Adrenal Hyperplasia
Marianne Jacob, Karen Lin-Su, Corinne Catarozoli, et al.
Hemolytic Anemia due to Glucose 6 Phosphate Dehydrogenase Deficiency Triggered by Type 1 Diabetes Mellitus
Burçe Orman, Semra Çetinkaya, Nergiz Öner, et al.
Tumor-induced Osteomalacia in a Boy with Maxillary Ossifying Fibroma
Ha Nguyen Thi, Cuong Pham Manh, Linh To Tuan, et al.
Neonatal Diabetes, Congenital Hypothyroidism, and Congenital Glaucoma Coexistence: A Case of GLIS3 Mutation
Emre Sarıkaya, Mustafa Kendirci, Mikail Demir, et al.
A Novel Pathogenic IGSF1 Variant in a Patient with GH and TSH Deficiency Diagnosed by High IGF-I Values at Transition to Adult Care
Aslı Derya Kardelen, Esin Karakılıç Özturan, Şükran Poyrazoğlu, et al.
A Novel Heterozygous NF1 Variant in a Neurofibromatosis-Noonan Syndrome Patient with Growth Hormone Deficiency: A Case Report
Si Qin, Yindi Zhang, Fadong Yu, et al.
Unfavorable Effects of Low-carbonhydrate Diet in a Pediatric Patient with Type 1 Diabetes Mellitus
Ceren Güleryüz, Ece Eker, Gülin Karacan Küçükali, et al.
In response to: “Letter to: Endocrinological Approach to Adolescents with Gender Dysphoria: Experience of a Pediatric Endocrinology Department in a Tertiary Center in Turkey”
Esin Karakılıç Özturan, Ayşe Pınar Öztürk, Firdevs Baş, et al.
