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

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

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

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

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

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

The Clinical Spectrum of Resistance to Thyroid Hormone Alpha in Children and Adults

Sezer ACAR, KORCAN DEMİR

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

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

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

Pediatric Primary Adrenal Insufficiency: A 21-year Single Center Experience

Emine ÇAMTOSUN, İsmail DÜNDAR, Ayşehan AKINCI, Nurdan ÇİFTÇİ

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

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

6q25.1-q25.3 Microdeletion in a Chinese Girl

Mian Ling Zhong, Ye-Mei Song, Chao Chun ZOU

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