Archives - Journal of Clinical Research ın Pediatric Endocrinology

Original Article 9

Letter to the Editor 2

Review

Traditional and New Methods of Bone Age Assessment-An Overview

Monika Prokop-Piotrkowska

Kamila Marszałek-Dziuba

Elżbieta Moszczyńska

Mieczysław Szalecki

Elżbieta Jurkiewicz

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Original Article

Pre-treatment Neutropenia in Children and Adolescents with Autoimmune Hyperthyroidism

Melissa Kaori S. Litao

Ana Gutierrez Alvarez

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Basal Serum Thyroxine Level should Guide Initial Thyroxine Replacement Dose in Neonates with Congenital Hypothyroidism

E. Nazlı Gönç

Ayfer Alikaşifoğlu

Sevilay Karahan

Nurgün Kandemir

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Evaluation of Children and Adolescents with Thyroid Nodules: A Single Center Experience

Selin Elmaoğulları

Şervan Özalkak

Semra Çetinkaya

İbrahim Karaman

Şenay Savaş-Erdeve

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An Evaluation of Glucagon Injection Anxiety and Its Association with the Fear of Hypoglycemia among the Parents of Children with Type 1 Diabetes

Serra Muradoğlu

Gül Yeşiltepe Mutlu

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Midkine: Utility as a Predictor of Early Diabetic Nephropathy in Children with Type 1 Diabetes Mellitus

Kotb Abbass Metwalley

Hekma Saad Farghaly

Magda Farghali Gabri

Safwat Mohamed Abdel-Aziz

Asmaa Mohamed Ismail

Duaa Mohamed Raafat

Islam Fathy Elnakeeb

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Long-term Clinical Follow-up of Patients with Familial Hypomagnesemia with Secondary Hypocalcemia

Elvan Bayramoğlu

Melikşah Keskin

Şenay Savaş-Erdeve

Semra Çetinkaya

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The Application of Next Generation Sequencing Maturity Onset Diabetes of the Young Gene Panel in Turkish Patients from Trakya Region

Sinem Yalçıntepe

Fatma Özgüç Çömlek

Emine İkbal Atlı

Filiz Tütüncüler Kökenli

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Evaluation of Growth Hormone Results in Different Diagnosis and Trend Over 10 Year of Follow-up: A Single Center Experience

Aslıhan Araslı Yılmaz

Şenay Savaş Erdeve

Semra Çetinkaya

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Case Report

Vandetanib in a Child Affected by Neurofibromatosis Type 1 and Medullary Thyroid Carcinoma with Both NF1 and Homozygous RET Proto-oncogen Germ-line Mutations

Begümhan Demir Gündoğan

Sevcan Tuğ Bozdoğan

Ferah Tuncel Daloğlu

Elvan Cağlar Çıtak

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Unusual Presentation of Denys-Drash Syndrome in a Girl with Undisclosed Consumption of Biotin

Germana Antonella Giannone

Jacopo Gervasoni

Sabina Benedetti

Federica Albanese

Luca Dello Strologo

Mafalda Mucciolo

Francesca Diomedi Camassei

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A Case of Congenital Central Hypothyroidism Caused by a Novel Variant (Gln1255Ter) in IGSF1 Gene

Doğa Türkkahraman

Nimet Karataş Torun

Nadide Cemre Randa

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Brain Abscess in a Patient with Osteopetrosis: A Rare Complication

Merve İşeri Nepesov

Kürşat Bora Çarman

Suzan Şaylısoy

Ener Çağrı Dinleyici

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Co-existence of Congenital Adrenal Hyperplasia and Familial Hypokalemic Periodic Paralysis due to CYP21A2 and SCN4A Pathogenic Variants

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Letter to the Editor

Analysis of the Performance of Neck Circumference to Identify Overweight and Obese Children

Manuel André Virú-Loza

In reply Asif M et al.