Archives - Journal of Clinical Research ın Pediatric Endocrinology

Original Article 9

Review

Specific Functions of Melanocortin 3 Receptor (MC3R)

Seyda Tugce Durhan

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Original Article

Factors Affecting Thyroid Elastography in Healthy Children and Patients with Hashimoto’s Thyroiditis

Serkan Bilge Koca

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Endocrine Abnormalities and Growth Characterization in Colombian Pediatric Patients with 22q11 Deletion Syndrome

Juan Lasprilla-Tovar

Nora Alejandra Zuluaga

Carolina Forero

Oscar Correa-Jiménez

Javier Mauricio Sierra

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Anomalies in Human Sex Determination: Usefulness of a Combined Cytogenetic Approach to Characterize an Additional Case with Xp Functional Disomy Associated with 46,XY Gonadal Dysgenesis

Ikbel Hadj Hassine

Hela Ben Khelifa

Kenneth Mcelreavey

Soumaya Mougou-Zerelli

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Clinical Utility and Outcome Prediction of Early ZnT8-IgG Testing and Titer in Type 1 Diabetes

Sarah Jenkins M.

Sean J. Pittock

Siobhan T. Pittock

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Comparison of Commonly Used Methods to Predict the Final Height in Constitutional Tall Stature

Alma Kamar Matias

Evgenia Muginshtein-Simkovitch

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Frequency, Clinical Characteristics and Predictors of Ketoacidosis at Diagnosis of Type One Diabetes Mellitus in Children and Adolescents from Jordan

Lobna Gharaibeh

Jumana Albaramki

Fatima Al Barakat

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The Relationship Between Premature Adrenarche and Platelet Aggregation

Mehmet Emre Taşçılar

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Factors Associated with Low Bone Mineral Density at the Time of Diagnosis in Children with Celiac Disease

Emine Çamtosun

Fatma İlknur Varol

Şükrü Güngör

Mukadder Ayşe Selimoğlu

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Increased Carotid Intima-media Thickness and Its Association with Carbohydrate Metabolism and Adipocytokines in Children Treated with Recombinant Growth Hormone

Mehmet Kocaağa

Şükran Poyrazoğlu

Rüveyde Bundak

Feyza Darendeliler

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Case Report

Weight Loss During Topiramate Treatment in a Severely Obese Adolescent with Congenital Adrenal Hyperplasia and Migraine

Heather M. Ross

Alaina P. Vidmar

Mitchell E. Geffner

Claudia Borzutzky

Nicole R. Fraga

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Rare Coexistence of Congenital Adrenal Hyperplasia due to 21-Hydroxylase Deficiency and Turner Syndrome: A Case Report and Brief Literature Review

Joana Serra-Caetano

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Expanding the Phenotype of TRMT10A Mutations: Case Report and a Review of the Existing Cases

Zeynep Şıklar

Kevin Colclough

Kashyap A. Patel

Merih Berberoğlu

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Compound Heterozygous Variants in FAM111A Cause Autosomal Recessive Kenny-Caffey Syndrome Type 2

Havva Tezcan Ünlü

Serdar Ceylaner

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Maltodextrin May Be a Promising Treatment Modality After Neartotal Pancreatectomy in Infants Younger Than Six Months with Persistent Hyperinsulinism: A Case Report

Yasemin Denkboy Öngen

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