Phenotype Heterogeneity in Glucokinase–Maturity-Onset Diabetes of the Young (GCK-MODY) Patients

• Anna Wedrychowicz
• Ewa Tobór
• Magdalena Wilk
• Ewa Ziólkowska-Ledwith
• Anna Rams
• Katarzyna Wzorek
• Barbara Sabal
• Malgorzata Stelmach
• Jerzy B. Starzyk

46,XY Disorder of Sex Development due to 17-Beta Hydroxysteroid Dehydrogenase Type 3 Deficiency in an Infant of Greek Origin

• Assimina Galli Tsinopoulou
• Anastasios Serbis
• Eleni P. Kotanidou
• Eleni Litou
• Vaia Dokousli
• Konstantina Mouzaki
• Pavlos Fanis
• Vassos Neocleous
• Nicos Skordis

Neonatal Hypopituitarism: Approaches to Diagnosis and Treatment

• Selim Kurtoğlu
• Ahmet Özdemir
• Nihal Hatipoğlu

Abnormal Uterine Bleeding In Adolescents

• Selin Elmaoğulları
• Zehra Aycan

Synchronous Solid Pseudopapillary Tumor and Insulinoma in an Adolescent MEN1 Patient Presenting with Diagnostic Dilemmas

• Ahmet Uçar
• Banu Özgüven
• Muharrem Battal
• Ferda Alparslan Pınarlı
• Evrim Özmen
• Aylin Yetim
• Yasin Yılmaz

Could Alerting Physicians for Low Alkaline Phosphatase Levels Be Helpful in Early Diagnosis of Hypophosphatasia?

• Asma Deeb
• Abubaker Elfatih

Effect of Maternal Obesity on Fetal Growth and Expression of Placental Fatty Acid Transporters

• Kui Ye
• Li Li
• Dan Zhang
• Yi Li
• Hai-Qing Wang
• Han-Lin Lai
• Chuan-Lai Hu

The Distribution of Different Types of Diabetes in Childhood: A Single Center Experience

• Belma Haliloğlu
• Saygın Abalı
• Fuat Buğrul
• Enes Çelik
• Serpil Baş
• Zeynep Atay
• Tülay Güran
• Serap Turan
• Abdullah Bereket

Evaluation of Efficacy of Long-term Growth Hormone Therapy in Patients with Hypochondroplasia

• Tuğba Çetin
• Zeynep Şıklar
• Pınar Kocaay
• Merih Berberoğlu

Childhood Sustained Hypercalcemia: A Diagnostic Challenge

• Nisa Eda Çullas İlarslan
• Zeynep Şıklar
• Merih Berberoğlu

Investigation of MKRN3 Mutation in Patients with Familial Central Precocious Puberty

• Zehra Aycan
• Şenay Savaş-Erdeve
• Semra Çetinkaya
• Erdal Kurnaz
• Melikşah Keskin
• Nursel Muratoğlu Şahin
• Elvan Bayramoğlu
• Gülay Ceylaner

Neonatal Diabetes: Two Cases with Isolated Pancreas Agenesis due to Homozygous PTF1A Enhancer Mutations and One with Developmental Delay, Epilepsy, and Neonatal Diabetes Syndrome due to KCNJ11 Mutation

• Olcay Evliyaoğlu
• Oya Ercan
• Emel Ataloğlu
• Ümit Zübarioğlu
• Bahar Özcabı
• Aydilek Dağdeviren
• Hande Erdoğan
• Elisa De Franco
• Sian Ellard

The Evaluation of Cases with Y-Chromosome Gonadal Dysgenesis: Clinical Experience over 18 Years

• Merih Berberoğlu
• Zeynep Şıklar
• Ankara University Faculty of Medicine Disorders of Sexual Development Ethics Committee

Letter to the Editor Regarding “Assessment of Retinal Nerve Fiber Layer Thickness in Non-Diabetic Obese Children and Adolescents”

• Ömer Karti

Acute Effects of Blood Transfusion on Insulin Sensitivity and Pancreatic β-Cell Function in Children with β-Thalassemia/Hemoglobin E Disease

• Somboon Wankanit
• Ampaiwan Chuansumrit
• Preamrudee Poomthavorn
• Patcharin Khlairit
• Sarunyu Pongratanakul
• Pat Mahachoklertwattana

The Relationship Between Glycemic Variability and Inflammatory Markers in Obese Children with Insulin Resistance and Metabolic Syndrome

• Abdurrahman Kaya
• Cemil Koçyiğit
• Gönül Çatlı
• Elif Büşra Özkan
• Bumin Nuri Dündar

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

• Nataliya Zelinska
• Iryna Shevchenko
• Evgenia Globa

Reliability and Validity of the Diabetes Eating Problem Survey in Turkish Children and Adolescents with Type 1 Diabetes Mellitus

• Yasemin Atik Altınok
• Suriye Özgür
• Reci Meseri
• Samim Özen
• Şükran Darcan
• Damla Gökşen

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 Panigrahi
• Balasubramaniyan Muthuvel
• Ashish Agarwal

Serum Thyroid-Stimulating Hormone Levels and Body Mass Index Percentiles in Children with Primary Hypothyroidism on Levothyroxine Replacement

• Asma Shaoba
• Sanjib Basu
• Stelios Mantis
• Carla Minutti

Can Fetuin-A Be a Marker for Insulin Resistance and Poor Glycemic Control in Children with Type 1 Diabetes Mellitus?

• Ülkü Gül Şiraz
• Murat Doğan
• Nihal Hatipoğlu
• Sabahattin Muhtaroğlu
• Selim Kurtoğlu

High Prenatal Exposure to Bisphenol A Reduces Anogenital Distance in Healthy Male Newborns

• Emil Mammadov
• Murat Uncu
• Ceyhun Dalkan

A Patient with Proopiomelanocortin Deficiency: An Increasingly Important Diagnosis to Make

• Semra Çetinkaya
• Tülay Güran
• Erdal Kurnaz
• Melikşah Keskin
• Elif Sağsak
• Senay Savaş Erdeve
• Jenifer P. Suntharalingham
• Federica Buonocore
• John C. Achermann
• Zehra Aycan

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?

• Emine Çamtosun
• Zeynep Şıklar
• Merih Berberoğlu

A Meta-Analysis and an Evaluation of Trends in Obesity Prevalence among Children and Adolescents in Turkey: 1990 through 2015

• Züleyha Alper
• İlker Ercan
• Yeşim Uncu

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

• Ali Duyu
• Elvan Çağlar Çıtak
• Erdem Ak
• Serhan Kupeli
• Begül Yağcı Küpeli
• İbrahim Bayram
• Gülay Sezgin
• Gülçin Eskendari
• Kerem Sezer

A Case of Autosomal Dominant Osteopetrosis Type 2 with a CLCN7 Gene Mutation

• Sol Kang
• Young Kyung Kang
• Jun Ah Lee
• Dong Ho Kim
• Jung Sub Lim

Response to Growth Hormone Treatment in a Patient with Insulin-Like Growth Factor 1 Receptor Deletion

• Ranim Mahmoud
• Ajanta Naidu
• Hiba Risheg
• Virginia Kimonis

Treatment of Pre-pubertal Patients with Growth Hormone Deficiency: Patterns in Growth Hormone Dosage and Insulin-like Growth Factor-I Z-scores

• Megan Oberle
• Adda Grimberg
• Vaneeta Bamba

Extreme Premature Small for Gestational Age Infants Have Appropriate Catch-up Growth at Term Equivalence Compared with Extreme Premature Appropriate for Gestational Age Infants

• Sze May Ng
• Donatella Pintus
• Mark A. Turner

Successful Growth Hormone Therapy in Cornelia de Lange Syndrome

• Michael de Graaf
• Sarina G Kant
• Jan Maarten Wit
• Egbert Johan Willem Redeker
• Gijs Willem Eduard Santen
• Annemieke Johanna Maria Henriëtta Verkerk
• André Gerardus Uitterlinden
• Monique Losekoot
• Wilma Oostdijk

ß-3AR W64R Polymorphism and 30-Minute Post-Challenge Plasma Glucose Levels in Obese Children

• Hasibe Verdi
• Sibel Tulgar Kınık
• Yaprak Yılmaz Yalçın
• Nursel Muratoğlu Şahin
• Ayşe Canan Yazıcı
• F. Belgin Ataç

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

• Caroline Ovadia
• Hanns-Ulrich Marschall
• Catherine Williamson

ROHHAD Syndrome, a Rare Cause of Hypothalamic Obesity: Report of Two Cases

• Ülkü Gül Şiraz
• Deniz Ökdemir
• Gül Direk
• Leyla Akın
• Nihal Hatipoğlu
• Mustafa Kendirci
• Selim Kurtoğlu

Vitamin D Deficiency in Pregnant Women and Their Infants

• Abdurrahman Avar Özdemir
• Yasemin Ercan Gündemir
• Mustafa Küçük
• Deniz Yıldıran Sarıcı
• Yusuf Elgörmüş
• Yakup Çağ
• Günal Bilek

An Assessment of Retinal Nerve Fiber Layer Thickness in Non-Diabetic Obese Children and Adolescents

• Bediz Özen
• Hakan Öztürk
• Gönül Çatlı
• Bumin Dündar

The Relationship Between Blood Pressure and Sleep Duration in Turkish Children: A Cross-Sectional Study

• Cengiz Bal
• Ahmet Öztürk
• Betül Çiçek
• Ahmet Özdemir
• Gökmen Zararsız
• Demet Ünalan
• Gözde Ertürk Zararsız
• Selçuk Korkmaz
• Dinçer Göksülük
• Vahap Eldem
• Sevda İsmailoğulları
• Emine Erdem
• Mümtaz M Mazıcıoğlu
• Selim Kurtoğlu

Tolvaptan Treatment in Children with Chronic Hyponatremia due to Inappropriate Antidiuretic Hormone Secretion: A Report of Three Cases

• Gerdi Tuli
• Daniele Tessaris
• Silvia Einaudi
• Luisa De Sanctis
• Patrizia Matarazzo

Is There an Association Between Cortisol and Hypertension in Overweight or Obese Children?

• Aleid JG Wirix
• Martijn JJ Finken
• Ines A von Rosenstiel-Jadoul
• Annemieke C Heijboer
• Jeroen Nauta
• Jaap W Groothoff
• Mai JM Chinapaw
• Joana E Kist-van Holthe

CYP21A2 Gene Mutations in Congenital Adrenal Hyperplasia: Genotype-phenotype correlation in Turkish children

• Firdevs Baş
• Hülya Kayserili
• Feyza Darendeliler
• Oya Uyguner
• Hülya Günöz
• Memnune Yüksel Apak
• Fatmahan Atalar
• Rüveyde Bundak
• Robert C. Wilson
• Maria I. New
• Bernd Wollnik
• Nurçin Saka

Iatrogenic Cushing’s Syndrome Following Short-Term Intranasal Steroid Use

• Deep Dutta
• Shivaprasad KS
• Sujoy Ghosh
• Satinath Mukhopadhyay
• Subhankar Chowdhury

The Relationship of Disordered Eating Attitudes with Stress Level, Bone Turnover Markers, and Bone Mineral Density in Obese Adolescents

• Aslı Okbay Güneş
• Müjgan Alikaşifoğlu
• Ezgi Şen Demirdöğen
• Ethem Erginöz
• Türkay Demir
• Mine Kucur
• Oya Ercan

Serum Nesfatin-1 Levels in Girls with Idiopathic Central Precocious Puberty

• Ayça Altıncık
• Oya Sayın

Optimal Cut-off Points of Fasting and Post-Glucose Stimulus Surrogates of Insulin Resistance as Predictors of Metabolic Syndrome in Adolescents According to Several Definitions

• Mónica Ivette Piña-Aguero
• Aranza Zaldivar-Delgado
• Alejandra Salas-Fernández
• Azucena Martínez-Basila
• Mariela Bernabe-Garcia
• Jorge Maldonado-Hernández

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

• Assimina Galli-Tsinopoulou
• Eleni P. Kotanidou
• Aggeliki N. Kleisarchaki
• Rivka Kauli
• Zvi Laron

Sirolimus-Induced Hepatitis in Two Patients with Hyperinsulinemic Hypoglycemia

• Belma Haliloğlu
• Heybet Tüzün
• Sarah E. Flanagan
• Muhittin Çelik
• Avni Kaya
• Sian Ellard
• Mehmet Nuri Özbek

CYP24A1 Mutation in a Girl Infant with Idiopathic Infantile Hypercalcemia

• Jens Otto Broby Madsen
• Sabrina Sauer
• Bodo Beck
• Jesper Johannesen

Hyperprolactinemia in Children with Subclinical Hypothyroidism

• Neera Sharma
• Deep Dutta
• Lokesh Kumar Sharma

Effectiveness of Continuous Subcutaneous Insulin Infusion Pump Therapy During Five Years of Treatment on Metabolic Control in Children and Adolescents with Type 1 Diabetes Mellitus

• Özlem Korkmaz
• Günay Demir
• Hafize Çetin
• İlkin Mecidov
• Yasemin Atik Altınok
• Samim Özen
• Şükran Darcan
• Damla Gökşen

A Novel Homozygous CYP19A1 Gene Mutation: Aromatase Deficiency Mimicking Congenital Adrenal Hyperplasia in an Infant without Obvious Maternal Virilisation

• Fatma Dursun
• Serdar Ceylaner