| The Clinical Spectrum of Resistance to Thyroid Hormone Alpha in Children and Adults | Sezer ACAR,KORCAN DEMİR | 1–14 |
| Catch-up Growth in Prepubertal Children Treated for Juvenile Hypothyroidism and Growth Hormone Deficiency can be Modelled with a Monomolecular Function | Jan Maarten WIT,Theo C. J. SAS,Michael B. RANKE,Paula van DOMMELEN | 15–22 |
| Quality of Life and Psychological Well-being in Children and Adolescents with Disorders of Sex Development | Birsen ŞENTÜRK PİLAN,Burcu ÖZBARAN,Didem ÇELİK,Tuğçe ÖZCAN,Samim ÖZEN,Damla GÖKŞEN,İbrahim ULMAN,Ali AVANOĞLU,Sibel TİRYAKİ,Hüseyin ONAY,Özgür ÇOĞULU,Ferda OZKINAY,ŞÜKRAN DARCAN | 23–33 |
| Identification of Three Novel and One Known Mutation in the WFS1 Gene in Four Unrelated Turkish Families: The Role of Homozygosity Mapping in the Early Diagnosis | Maha SHERİF,Hüseyin DEMİRBİLEK,Atilla ÇAYIR,Sophia TAHIR,Büşranur ÇAVDARLI,Meliha DEMİRAL,Ayşe Nurcan CEBECİ,Doğuş VURALLI,Sofia Asim RAHMAN,Edip ÜNAL,Gönül BÜYÜKYILMAZ,Rıza Taner BARAN,Mehmet Nuri ÖZBEK,Khalid HUSSAİN | 34–43 |
| Very High Incidence of Type 1 Diabetes Among Children Aged Under 15 Years in Tlemcen, Northwest Algeria (2015-2018) | Sarra KHATER,Ammaria AOUAR,Nawel BENSMAIN,Salih BENDEDOUCHE,Nafissa CHABNI,Houari HAMDAOUI,Abdellatif MOUSSOUNI,Zakarya MOQADDEM | 44–51 |
| A New Cause of Obesity Syndrome Associated with a Mutation in the Carboxypeptidase Gene Detected in Three Siblings with Obesity, Intellectual Disability and Hypogonadotropic Hypogonadism | Hepsen Mine SERİN,Ayça AYKUT,TAHİR ATİK,Samim ÖZEN,Durdugül Ayyıldız EMECEN,Aysun ATA,Esra IŞIK,Damla GÖKŞEN,Özgür ÇOĞULU,Ferda OZKINAY | 52–60 |
| Transforming Growth Factor-β1 and Receptor for Advanced Glycation End Products Gene Expression and Protein Levels in Adolescents with Type 1 Diabetes Mellitus | Ana NINIC,Dragana BOJANİN,Miron SOPİ,Marija MİHAJLOVİ,Jelena MUNJAS,Tatjana MİLENKOVİ,Aleksandra STEFANOVİ,Jelena VEKİ,Vesna Spasojevi KALİMANOVSKA | 61–71 |
| Frequency of Celiac Disease and Spontaneous Normalization Rate of Celiac Serology in Children and Adolescent Patients with Type 1 Diabetes | Edip ÜNAL,Meliha DEMİRAL,Birsen BAYSAL,Mehmet AGIN,Elif Gökçe DEVECİOĞLU,Hüseyin DEMİRBİLEK,Mehmet Nuri ÖZBEK | 72–79 |
| Genotype and Phenotype Heterogeneity in Neonatal Diabetes: A Single Centre Experience in Turkey | Yasemin DENKBOY ÖNGEN,Erdal EREN,Özgecan DEMİRBAŞ,Elif SOBU,Sian ELLARD,Elisa De FRANCO,Ömer TARIM | 80–87 |
| Pediatric Primary Adrenal Insufficiency: A 21-year Single Center Experience | Emine ÇAMTOSUN,İsmail DÜNDAR,Ayşehan AKINCI,Nurdan ÇİFTÇİ | 88–99 |
| Homozygous Mutation in the Insulin Receptor Gene Associated with Mild Type A Insulin Resistance Syndrome: A Case Report | Bülent HACIHAMDİOĞLU,Elif Gülşah BAŞ,Kenan DELİL | 100–103 |
| The Unusual Case of Fibroma of Tendon Sheath in a Young Girl with Turner Syndrome Undergoing Growth Hormone Treatment | Yong Hee HONG,Dong Gyu KİM,Jong Hyun LEE,Min Jung JUNG,Chang Yong CHOİ | 104–108 |
| 6q25.1-q25.3 Microdeletion in a Chinese Girl | Mian Ling Zhong, Ye-Mei Song, Chao Chun ZOU | 109–113 |
| Treatment Difficulties in Hypomagnesemia Secondary to the Transient Receptor Potential Melastatin 6 Gene: A Case Report with Novel Mutation | Serdar CEYLANER, Senay SAVAŞ ERDEVE, Çiğdem Genç SEL, Hüsniye YÜCEL, Saliha ŞENEL, Gülin KARACAN KÜÇÜKALİ, Çiğdem Seher KASAPKARA, Ülkühan ÖZTOPRAK | 114–118 |
| Sirolimus Therapy and Follow-up in a Patient with Severe Congenital Hyperinsulinism Following Subtotal Pancreatectomy | Qiong Chen, Yongxing Chen, Haihua Yang, Xiaohong Wang, Yingxian Zhang, Xiaojing Liu, Yun Yan, Haiyan Wei | 119–123 |