Ahead of Print

Current Issue

Volume 17, Issue 1

January 2025

Current Issue Ahead of Print Archives

Original Article 22

Research Article 5

Letter to the Editor 1

Case Report

Clinical and Genetic Analyses of Two Unrelated 46, XX Girls with Combined 17α-Hydroxylase/17,20-lyase Deficiency from China

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Exploring Multiple Endocrinological Issues and Dysautonomia in a Rare Case: Hypoparathyroidism in MIRAGE Syndrome

Sirmen Kızılcan Çetin

Zeynep Şıklar

Hasan Fatih Çakmaklı

Gizem Şenyazar

Serdar Ceylaner

Merih Berberoğlu

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Adult Outcome After Partial Androgen Insensitivity Syndrome: Diagnosed and Assigned Female in Infancy

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A Rare Presentation of 17α Hydroxylase/17,20 Lyase Deficiency in a Patient with non-Hodgkin’s Lymphoma: A Case Report

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Unraveling the Genetic Puzzle: Could MAP3K7 Be a Candidate Gene for RASopathies? Case Presentation

Sirmen Kizilcan Cetin

Serdar Ceylaner

Merih Berberoğlu

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Identification of a Novel IGSF1 Variant in Two Malaysian Male Siblings with Central Hypothyroidism and Macroorchidism

Karuppiah Thilakavathy

Nurul Huda Musa

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Autosomal Recessive Hypophosphatemic Rickets Type 2 Associated with a Novel ENPP1 Variant in a Taiwanese Girl

Meng Ju Melody Tsai

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Cabergoline Induced Pathological Gambling in an Adolescent with Prolactinoma

Ozlem Nida Erbasi

Aslı Derya Kardelen

Sukran Poyrazoglu

Feyza Darendeliler

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A Rare Coexistence of Turner Syndrome and Mycosis Fungoides: A Case Report

Ozge Bayrak Demirel

Esin Karakilic-Ozturan

Sule Ozturk Sari

Asli Derya Kardelen Al

Sukran Poyrazoglu

Feyza Darendeliler

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Lymphocytic Infundibuloneurohypophysitis Diagnosis Owing to Positive Anti-rabphilin-3A Antibody Test Result in an 8-year-old Boy with Early-onset Central Diabetes İnsipidus

Haruki Fujisawa

Yoshihisa Sugimura

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Hyperinsulinemia in Sotos Syndrome with a de novo NSD1 Deletion

Magnus Burstedt

Irina Golovleva

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A Rare Cause of Neonatal Salt Wasting Syndrome: Clinical Management of a Case Diagnosed with Pseudohypoaldosteronism Due to a Novel Homozygous Variant in the SCNN1B Gene

Zeynep Donbaloğlu

Ebru Barsal Çetiner

Kürşat Çetin

Nurten Özkan Zarif

Özden Altıok Clark

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Floating-Harbor Syndrome in a Korean Patient with Short Stature and Early Puberty: A Case Report

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Insulinoma Associated with MEN1 Syndrome: A Case of Persistent Hypoglycemia in School-aged Child

Rodrigo Lemus-Zepeda

Aura María Salazar-Solarte

Diana Marcela Vasquez-Forero

Liliana Mejía-Zapata

Mario Jr. Angulo-Mosquera

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Pituitary Stalk Interruption Syndrome – Clinical Presentation and Management of a Potentially Life-threatening Disease in Newborns

Elisabeth Steichen

Peter Wöckinger

Ursula Kiechl-Kohlendorfer

Elke Griesmaier

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Sotos Syndrome and Nephrocalcinosis, a Rare But Possible Association due to Impact on Contiguous Genes

Juan D. González-Rodríguez

Esther Q. Inglés-Torres

José E. Cabrera-Sevilla

Salvador Ibáñez-Micó

Francisca Bermejo-Costa

Ascensión Vera-Carbonell

Juan A. Bafalliu-Vidal

Pedro Cortés-Mora

Ana Lorente-Nicolás

José María Donate-Legaz

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Hereditary Severe Insulin-resistance Syndrome and Acanthosis Nigricans Caused by Novel Mutations in the INSR Gene

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Novel Variant of SLC34A3 in a Compound Heterozygous Brazilian Girl with Hereditary Hypophosphatemic Rickets with Hypercalciuria

Luciana Pinto Valadares

Daniel Rocha de Carvalho

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Permanent Neonatal Diabetes with High Insulin Requirements Due to a New Variant in the INS Gene

Johana Andrea Botero Hernández

Gina González-Valencia

Gabriel del Castillo

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A Rare Cause Of Proportional Short Stature and Puberty Precocity: Floating-Harbor Syndrome

Duygu Çetinkaya

Gönül Büyükyılmaz

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Early-onset Chronic Keratitis as the First Presenting Component of Autoimmune Polyendocrinopathy Syndrome Type 1 (APS-1): A Case Report and Review of the Literature

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Familial Clinical Heterogeneity of Medullary Thyroid Cancer with Germline RET S891A Protooncogene Mutation: 7-Year Follow-up with Successful Sorafenib Treatment

Sirmen Kizilcan Cetin

Ayca Kırmızı

Handan Dincaslan

Merih Berberoğlu

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A 15-year-old Girl with a Lateral Neck Mass Turning Out to Be Papillary Thyroid Carcinoma-Lateral Ectopic Papillary Thyroid Carcinoma or Lymph Node Metastasis?

Marijke E.B. Kremer

A. S. Paul van Trotsenburg

Anton F. Engelsman

Esther Edelenbos

Arantza Farina-Sarasqueta

Joost van Schuppen

José C.C. Koppes

Joep P.M Derikx

Christiaan F. Mooij

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Atypical Presentation and Course of ACTH-independent Cushing’s Syndrome in Two Families

Kübra Yüksek Acinikli

Özgür Kırbıyık

Gözde Akın Kağızmanlı

Deniz Kızmazoğlu

Kutsal Yörükoğlu

Handan Güleryüz

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Acute Kidney Injury After Thyroid Hormone Withdrawal in an Adolescent with Papillary Thyroid Carcinoma

Rüveyda Gülmez

Gürkan Tarçın

Dilek Bingöl Aydın

Olcay Evliyaoğlu

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Diazoxide-unresponsive Hyperinsulinemic Hypoglycaemia in a Preterm Infant with Heterozygous Insulin Receptor Gene Mutation

Sarah Wing-yiu POON

Brian Hon-yin CHUNG

Mabel Siu-chun WONG

Anita Man-ching TSAN

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A Challenging Case of Ectopic ACTH Syndrome with Bronchial Carcinoid and Literature Review

Sema Nilay ABSEYİ

Ayten KAYI CANGIR

Emel CABİ ÜNAL

Nurdan TAÇYILDIZ

Merih BERBEROĞLU

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Worsening of Congenital Hypothyroidism After Start of Carob-bean Gum Thickened Formula: Is There a Link? A Case Report

Claudia Signorino

Giovanna Municchi

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Continuous Glucose Monitoring Systems and the Efficacy of Acarbose Treatment in Cystic Fibrosis-related Dysglycemia

Emrullah Arslan

Deniz Ozalp Kızılay

Yasemin Atik Altinok

Bahar Girgin Dundar

Ruhsar Damla Goksen

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Schwartz-Jampel Syndrome Type-1: Compound Heterozygosity of Two Novel Variants

Fatma Güliz Atmaca

Özlem Akgün Doğan

Büşra Kutlubay

Heves Kırmızıbekmez

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The First Case of 4H Syndrome with Type 1 Diabetes Mellitus

Gonul Buyukyilmaz

Busra Erozan Cavdarlı

Keziban Toksoy Adiguzel

Mehmet Adiguzel

Cigdem Seher Kasapkara

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A Rare Case of Monogenic Obesity due to a Novel Variant in the ADCY3 Gene: Challenges in Follow-up and Treatment

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Hereditary Pheochromocytoma as a Main Manifestation of von Hippel Lindau Disease (vHL) in Childhood – A Long-term Follow-up of 5 Patients with vHL from One Family

Katarzyna Pasternak-Pietrzak

Agata Kozlowska

Elzbieta Moszczynska

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A Boy with 46,XX Karyotype (SRY double-positive) having a Leydig Cell Tumor

Tangül PINARCI

Doğa TURKKAHRAMAN

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Gonadoblastoma with Dysgerminoma in a Virilized Adolescent with Karyotype 46,XX: A Case Report and Review of the Literature

Tuğçe Kandemir

Esin Karakilic Ozturan

Ayça Dilruba Aslanger

Elif İnan Balcı

Aslı Derya Kardelen Al

Şükran Poyrazoğlu

Feyza Darendeliler

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Diagnostic Pitfalls of a Newborn with Congenital Nephrogenic Diabetes Insipidus

Heves Kırmızıbekmez

Özlem Akgün Doğan

Leyla Karadeniz Bilgin

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A Rare Cause of Hypergonadotropic Hypogonadism: Transaldolase Deficiency in Two Siblings

Tugce Goksu Kabil

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Original Article

Is Automated Insulin Delivery System Therapy Safe and Effectıve in Children Under 7 Years Old?

Deniz Ozalp Kizilay

Yasemin Atik Altinok

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Current Practices in Hashimoto's Thyroiditis: Differences in Attitudes Between Pediatric and Adult Endocrinologists in Türkiye: A National Survey

Gul Yesiltepe Mutlu

Aydilek Dagdeviren Cakır

Thyroid Working Group

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The Impact of the 2023 Turkey Earthquakes on Glycemic Control and Stress Levels in Children with Type 1 Diabetes: Single-center Experience

Seda Aybüke Sarı

Simge Bilaloğlu

Şeyma Demiray Güllü

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Machine Learning-driven Identification of the Honeymoon Phase in Pediatric Type 1 Diabetes and Optimizing Insulin Management

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Inequalities in Access to Diabetes Technologies in Children with Type 1 Diabetes: A Multicenter, Cross-sectional Study from Türkiye

Kagan Ege Karakus

Ruken Yıldırım

Şervan Özalkak

Mehmet N. Özbek

Nurdan Yıldırım

Gülcan Delibağ

Beray S. Eklioğlu

Belma Haliloğlu

Heves Kırmızıbekmez

Gül Yeşiltepe-Mutlu

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Endocrine Disorders in Children with Primary Mitochondrial Diseases: Single-Center Experience

Esra Deniz PAPATYA ÇAKIR

Nihan ÇAKIR BİÇER

Asuman GEDİKBAŞI

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Diagnostic Challenge of Phenotypic Variability in COL2A1-Related Disorders: Four Novel Variants and Expanding the Clinical Spectrum

Yasemin Kendir Demirkol

Ahmet Hamdi Akgülle

Heves Kırmızıbekmez

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Normative Values for Thyroid Volume and Tracheal Index in Healthy Turkish Newborns in an Iodine Sufficient Region

Reyhan DEVECİ SEVİM

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ACTION Teens Global Survey-Türkiye Report: More Worry and Less Motivation for Adolescents Living with Obesity

Abdullah Bereket

Neşe Perdahlı Fiş

Belma Haliloğlu

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Clinical Characteristics and Genotype-Phenotype Correlation in the Patients with the Diagnosis of Resistance to Thyroid Hormone Beta

Gönül Büyükyılmaz

Büşranur Çavdarlı

Serkan Bilge Koca

Keziban Toksoy Adıgüzel

Nur Semerci Gündüz

Hüseyin Demirbilek

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Serum Neudesin Levels in Patients with Congenital Hypothyroidism

İlker Tolga Özgen

Caner Yıldız3, Ömer Faruk Özer

Emel Hatun Aytaç Kaplan

Zümrüt Kocabey Sütçü

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Could MOTS-C Levels in Children with Type 1 Diabetes Mellitus Be an İndicator for Early Diabetic Kidney Disease?

İlknur Girisgen

Selda Ayça Altıncık

Gaye Malaş Öztekin

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Adaptation/Validity-reliability Evaluation of Menstruel Bleeding Questionnaire to Turkish Adolescent Girls

Aşan Önder Çamaş

Hamdi Cihan Emeksiz

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The Effect of Parental Collaboration on Diabetes Self-Efficacy, Quality of Life and HbA1c Level in Adolescents Diagnosed with Type 1 Diabetes

Beste Özgüven Öztornacı

Esra Ardahan Akgül

Hatice Yıldırım Sarı

Bumin Nuri Dündar

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Hospital Admission for Diabetic Ketoacidosis in Thai Children and Adolescents with Type 1 Diabetes: A National Study during 2015-2019

Somboon Wankanit

Kaewjai Thepsuthammarat

Preamrudee Poomthavorn

Taninee Sahakitrungruang

Pat Mahachoklertwattana

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Liraglutide Treatment Improves Glycaemic Dysregulation, Body Composition, Cardiometabolic Variables and Uncontrolled Eating Behaviour in Adolescents with Severe Obesity

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The Effect of Dietary Acid Load on Cardiometabolic Risk, Psychological Resilience and Sleep Quality in Adolescents with Obesity

Rukiye Bozbulut

Mahmut Orhun Çamurdan

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Germ Cell Dysfunction is Universal in Male Patients with β-Thalassemia Following Hematopoietic Stem Cell Transplantation During Childhood and Adolescence

Nuttha Piriyapokin

Pat Mahachoklertwattana

Preamrudee Poomthavorn

Usanarat Anurathapan

Wararat Chiangjong

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Evaluation of Arrhythmia Risk in Children with Type 1 Diabetes Mellitus

Yasemin ÖZDEMİR ŞAHAN

Gönül BÜYÜKYILMAZ

Oğuzhan DOĞAN

İbrahim İlker ÇETİN

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Experience in a PHTS Expertise Centre: Yield of Thyroid Ultrasound Surveillance in Children with PTEN Hamartoma Tumor Syndrome

Esther M.G. Bormans

Janneke H.M. Schuurs-Hoeijmakers

Petra van Setten

Linda A.J. Hendricks

Meggie M.C.M. Drissen

Martin Gotthardt

Hedi L. Claahsen-van der Grinten

Nicoline Hoogerbrugge

Jolanda H. Schieving

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Review

Gender Difference and Changes in the Prevalence of Obesity Over Time in Children Under 12 Years Old: A Meta-analysis

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Noonan Syndrome, Cancer Risk, and Growth Hormone Treatment

Kübra Yüksek Acınıklı

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Endocrine Implications of Congenital Disorders of Glycosylation

Zeynep Alev Özön

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Long-acting Growth Hormone Therapy, Rational and Future Aspects

Semra Çetinkaya

Furkan Erdoğan

Feyza Darendeliler

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Expanding the Clinical Features of Schimke Immuno-Osseous Dysplasia: A New Patient with a Novel Variant and Novel Clinical Findings

Sevgi Bilgiç Eltan

Asena Pınar Sefer

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Approach to Newborns with Elevated TSH: A Different Perspective from the International Guidelines for Iodine-Deficient Countries

Hüseyin Anıl Korkmaz

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Pediatric Type 1 Diabetes Care in Indonesia: A Review of Current Challenges and Practice

Ghaisani Fadiana

Helena Arnetta Puteri

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Research Article

Evaluation of Heavy Menstrual Bleeding in Adolescents

Tuğba Kontbay Çetin

Zuhal Keskin Sarılar

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Assessment of Quadriceps Muscle Strength and Thickness in Adolescents with Polycystic Ovary Syndrome: A Case-control and Longitudinal Follow-up Study

Ayşe Gül Güven

Demet Aygün Arı

Erdem Karabulut

Hüseyin Demirbilek

Gürkan Bozdağ

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Attitudes Towards the Management of Congenital Hypothyroidism in Türkiye: National Survey Study

Aydilek Dagdeviren Cakır

Gul Yesiltepe Mutlu

Thyroid Research Group

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Automatic Bone Age Determination in Adult Height Prediction for Girls with Early Variants Puberty and Precoccious Puberty

Murat Huseyin Yigit

Gul Yesiltepe Mutlu

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Frequency of “PCOS” and “Being at Risk for PCOS” in Obese Adolescent Girls in Light of Current Definitions

Fatma Güliz Atmaca

Esma Ebru Altun

Heves Kırmızıbekmez

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Letter to the Editor

Can Dietary Acid Load in Obese Adolescents Interfere with Cardiometabolic Risk, Psychological Resilience and Sleep Quality?

Nadia Raci Marques Pereira

Andreia Bezerra

WITHDRAWN

WITHDRAWN: Triglyceride Glucose Index as a Surrogate Measure of Insulin Sensitivity in a Caucasian Pediatric Population

Valeria Calcaterra

Chiara Montalbano

Annalisa de Silvestri

Corrado Regalbuto

Valeria Paganelli

Riccardo Albertini

Francesco Delle Cave

Daniela Larizza

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