A Synopsis of Current Practice in the Diagnosis and Management of Patients with Turner Syndrome in Turkey: A Survey of 18 Pediatric Endocrinology Centers

Ahmet UÇAR, AYHAN ABACI, MUSTAFA ÖZGÜR PİRGON, BUMİN NURİ DÜNDAR, FİLİZ TÜTÜNCÜLER KÖKENLİ, GÖNÜL ÇATLI, AHMET ANIK, Aylin KILINÇ UĞURLU, Atilla BÜYÜKGEBİZ

Peripheral Neuropathy as a Complication of Diabetic Ketoacidosis in a Child with Newly Diagnosed Diabetes Type 1: A Case Report

Marta BASZYNSKA-WİLK, Marta WYSOCKA-MİNCEWİCZ, Anna ŚWİERCZ, Jolanta ŚWİDERSKA, Magdalena MARSZAł, Mieczysław SZALECKİ

The Importance of Gestation-Adjusted Birthweight Centile in Assessment of Fetal Growth in Metabolic Conditions

Caroline OVADİA, Hanns-Ulrich MARSCHALL, Catherine WİLLİAMSON

Abnormal Uterine Bleeding in Adolescents

Selin ELMAOĞULLARI, ZEHRA AYCAN

A Rare Cause of Congenital Adrenal Hyperplasia: Clinical and Genetic Findings and Follow-up Characteristics of Six Patients with 17-Hydroxylase Deficiency Including Two Novel Mutations

Aslı Derya KARDELEN, Güven TOKSOY, FİRDEVS BAŞ, Zehra Yavaş ABALI, Genco GENÇAY, ŞÜKRAN POYRAZOĞLU, Rüveyde BUNDAK, Umut ALTUNOĞLU, Şahin AVCI, Adam NAJAFLI, ZEHRA OYA UYGUNER, BİRSEN KARAMAN, SEHER BAŞARAN, FATMA FEYZA DARENDELİLER

Subnormal Growth Velocity and Related Factors During GnRH Analog Therapy for Idiopathic Central Precocious Puberty

Nursel MURATOĞLU ŞAHİN, ASİYE UĞRAŞ DİKMEN, SEMRA ÇETİNKAYA, ZEHRA AYCAN

Nationwide Study of Turner Syndrome in Ukrainian Children: Prevalence, Genetic Variants and Phenotypic Features

Nataliya ZELİNSKA, Iryna SHEVCHENKO, Evgenia GLOBA

Parental Perception of Terminology of Disorders of Sex Development in Western Turkey

Sibel TİRYAKİ, ALİ TEKİN, İSMAİL YAĞMUR, SAMİM ÖZEN, Burcu ÖZBARAN, RUHSAR DAMLA GÖKŞEN ŞİMŞEK, ŞÜKRAN DARCAN, İBRAHİM ULMAN, Ali AVANOĞLU

Resolution of Consumptive Hypothyroidism Secondary to Infantile Hepatic Hemangiomatosis with a Combination of Propranolol and Levothyroxine

Victoria CAMPBELL, Rachel BECKETT, Noina ABİD, Susannah HOEY

Investigation of MKRN3 Mutation in Patients with Familial Central Precocious Puberty

ZEHRA AYCAN, ŞENAY SAVAŞ ERDEVE, SEMRA ÇETİNKAYA, Erdal KURNAZ, Melikşah KESKİN, Nursel MURATOĞLU ŞAHİN, Elvan BAYRAMOĞLU, Gülay CEYLANER

Prospective Follow-up of Children with Idiopathic Growth Hormone Deficiency After Termination of Growth Hormone Treatment: Is There Really Need for Treatment at Transition to Adulthood?

EMİNE ÇAMTOSUN, ZEYNEP ŞIKLAR, MERİH BERBEROĞLU

Neonatal Features of the Prader-Willi Syndrome; The Case for Making the Diagnosis During the First Week of Life

FİLİZ MİNE ÇİZMECİOĞLU, Jeremy Huw JONES, Wendy Forsyth PATERSON, Sakina KHERRA, Mariam KOURİME, Ruth MCGOWAN, M. Guftar SHAİKH, Malcolm DONALDSON

Severe Early Onset Obesity due to a Novel Missense Mutation in Exon 3 of the Leptin Gene in an Infant from Northwest India

Devi DAYAL, Keerthivasan SEETHARAMAN, Inusha PANİGRAHİ, Balasubramaniyan MUTHUVEL, Ashish AGARWAL

Sirolimus-Induced Hepatitis in Two Patients with Hyperinsulinemic Hypoglycemia

Belma HALİLOĞLU, Heybet TÜZÜN, Sarah E FLANAGAN, Muhittin ÇELİK, Avni KAYA, Sian ELLARD, Mehmet Nuri ÖZBEK

A Novel Variant c.97C>T of the Growth Hormone Releasing Hormone Receptor Gene Causes Isolated Growth Hormone Deficiency Type Ib

Assimina GALLİ-TSİNOPOULOU, Eleni P. KOTANİDOU, Aggeliki N. KLEİSARCHAKİ, Rivka KAULİ, Zvi LARON

Prevalence and Related Factors of Euthyroid Sick Syndrome in Children with Untreated Cancer According to Two Different Criteria

Ali DUYU, ELVAN ÇAĞLAR ÇITAK, Erdem AK, SERHAN KÜPELİ, Begül YAĞCI KÜPELİ, İBRAHİM BAYRAM, GÜLAY SEZGİN, Gülçin ESKENDARİ, KEREM SEZER