Archives - Journal of Clinical Research ın Pediatric Endocrinology

Original Research 10

Short Communication 1

Original Research

Clinicopathological Characteristics of Papillary Thyroid Cancer in Children with Emphasis on Pubertal Status and Association with BRAFV600E Mutation

Şükran Poyrazoğlu

Rüveyde Bundak

Gülçin Yeğen

Yasemin Şanlı

Feyza Darendeliler

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Congenital Hyperinsulinism in China: A Review of Chinese Literature Over the Past 15 Years

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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

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

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Melanocortin-4 Receptor Gene Mutations in a Group of Turkish Obese Children and Adolescents

Fatma Ajlan Tükün

Özlem Nalbantoğlu

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Management of Childhood Thyroid Nodules: Surgical and Endocrinological Findings in a Large Group of Cases

Zafer Dökümcü

Damla Gökşen Şimşek

Şükran Darcan

Nazan Çetingül

Bengü Demirağ

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Clinical and Genetic Findings of Turkish Hypophosphatasia Cases

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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

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

Anna Wedrychowicz

Ewa Ziólkowska-Ledwith

Katarzyna Wzorek

Malgorzata Stelmach

Jerzy B. Starzyk

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The Relationship Between Perceived Family Climate and Glycemic Control in Type 1 Diabetes Mellitus Adolescent Patients

Halit Necmi Uçar

Fatma Çetinkaya

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Short Communication

An ABCC8 Nonsense Mutation Causing Neonatal Diabetes Through Altered Transcript Expression

Sarah E. Flanagan

Jayne A. L. Houghton

Elisa De Franco

Can Thi Bich Ngoc

Frances M. Ashcroft

Lorna W. Harries

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Case Report

Pituitary Adenoma Apoplexy in an Adolescent: A Case Report and Review of the Literature

Sebastian Schagen

Jan Maarten Wit

Nienke Biermasz

Wouter van Furth

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Pancreatic Agenesis due to Compound Heterozygosity for a Novel Enhancer and Truncating Mutation in the PTF1A Gene

Elisa De Franco

Regina S. Moisés

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Congenital Central Hypothyroidism Caused by a Novel Thyroid-Stimulating Hormone-Beta Subunit Gene Mutation in Two Siblings

Özlem Boz Anlaş

Bilge Sarıkepe

Nur Semerci Gündüz

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Long-Term Follow-up of a Case with Proprotein Convertase 1/3 Deficiency: Transient Diabetes Mellitus with Intervening Diabetic Ketoacidosis During Growth Hormone Therapy

E. Nazlı Gönç

Ayfer Alikaşifoğlu

Nurgün Kandemir

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

Daniele Tessaris

Luisa De Sanctis

Patrizia Matarazzo

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