AUTHOR INDEX

A B C Ç D E F G H I İ J K L M N O Ö P R S Ş T U Ü V Y Z
Çetinkaya

Semra Çetinkaya

Insulin Oedema in Newly Diagnosed Type 1 Diabetes Mellitus - Case Report

(J Clin Res Pediatr Endocrinol 2010; 2: -)

Hypothyroidism Due to Hepatic Hemangioendothelioma: A Case Report

(J Clin Res Pediatr Endocrinol 2010; 2: -)

Sporadic Nonautoimmune Neonatal Hyperthyroidism Due to A623V Germline Mutation in the Thyrotropin Receptor Gene-Case Report

(J Clin Res Pediatr Endocrinol 2010; 2: -)

Eight-Year Follow-up of a Girl with McCune-Albright Syndrome - Case Report

(J Clin Res Pediatr Endocrinol 2011; 3: -)

Assessment of the Knowledge of Diabetes Mellitus Among School Teachers within the Scope of the Managing Diabetes at School Program

(J Clin Res Pediatr Endocrinol 2012; 4: -)

A Rare Combination: Congenital Adrenal Hyperplasia Due To 21 Hydroxylase Deficiency and Turner Syndrome

(J Clin Res Pediatr Endocrinol 2012; 4: -)

Diabetes Care, Glycemic Control, Complications, and Concomitant Autoimmune Diseases in Children with Type 1 Diabetes in Turkey: A Multicenter Study

(J Clin Res Pediatr Endocrinol 2013; 5: -)

Hyperinsulinemic Hypoglycemia: Experience in A Series of 17 Cases

(J Clin Res Pediatr Endocrinol 2013; 5: -)

Long-Term Follow-Up of Cushing’s Disease: A Case Report

(J Clin Res Pediatr Endocrinol 2013; 5: -)

Evaluation of Asymmetric Dimethylarginine (ADMA) Levels in Children with Growth Hormone Deficiency

(J Clin Res Pediatr Endocrinol 2014; 6: -)

The Growth Characteristics of Patients with Noonan Syndrome: Results of Three Years of Growth Hormone Treatment: A Nationwide Multicenter Study

(J Clin Res Pediatr Endocrinol 2016; 8: 305-312)

A Rare Cause of Short Stature: 3M Syndrome in a Patient with Novel Mutation in OBSL1 Gene

(J Clin Res Pediatr Endocrinol 2017; 9: 91-94)
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