AUTHOR INDEX

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Çatlı

Gönül Çatlı

Epidemiology, Classification and Management of Undescended Testes: Does Medication Have Value in its Treatment?

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

Acute Vitamin D Intoxication Possibly Due to Faulty Production of a Multivitamin Preparation

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

46,XX Male Disorder of Sexual Development: A Case Report

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

Acceleration of Puberty During Growth Hormone Therapy in a Child with Septo-Optic Dysplasia

(J Clin Res Pediatr Endocrinol 2014; 6: 116-118)

A Case of Central Precocious Puberty Due to Concomitant Hypothalamic Hamartoma and Juvenile Pilocytic Astrocytoma

(J Clin Res Pediatr Endocrinol 2014; 6: 183-186)

Adipokines in Breast Milk: An Update

(J Clin Res Pediatr Endocrinol 2014; 6: 192-201)

The Effect of L-Thyroxine Treatment on Hypothyroid Symptom Scores and Lipid Profile in Children with Subclinical Hypothyroidism

(J Clin Res Pediatr Endocrinol 2014; 6: 238-244)

Turner Syndrome and Associated Problems in Turkish Children: A Multicenter Study

(J Clin Res Pediatr Endocrinol 2015; 7: 27-36)

Recovery of Central Fever after GH Therapy in a Patient with GH Deficiency Secondary to Posttraumatic Brain Injury

(J Clin Res Pediatr Endocrinol 2015; 7: 77-79)

An Unusual Presentation of 46,XY Pure Gonadal Dysgenesis: Spontaneous Breast Development and Menstruation

(J Clin Res Pediatr Endocrinol 2015; 7: 159-162)

Investigation of Genes That are Defined with New Generation Sequence Analysis in Children/Adolescents Followed with Maturity Onset Diabetes of the Young

(J Clin Res Pediatr Endocrinol 2015; 7: 46-46)

An Early Spontaneous Recovery in a Hyperinsulinemia and Hypoglycemia Case with a Recently Found Mutation on the Gene ABCC8

(J Clin Res Pediatr Endocrinol 2015; 7: 47-47)

A New Mutation on the SFR1 (NR5A1) Gene in a 46 XY Sexual Development Disorder Case without the Adrenal Deficiency

(J Clin Res Pediatr Endocrinol 2015; 7: 57-57)

Neonatal Diabetes Mellitus due to a Novel Mutation in the GATA6 Gene Accompanying Renal Dysfunction: A Case Report

(J Clin Res Pediatr Endocrinol 2015; 7: 63-63)

A Case of Achondrogenesis Type 2/Hypochondrogenesis Due to a De Novo Mutation in the COL2A1 Gene

(J Clin Res Pediatr Endocrinol 2015; 7: 80-80)

A Family with Multiple Endocrine Neoplasia Type 2A: Importance of Early Prophylactic Thyroidectomy

(J Clin Res Pediatr Endocrinol 2015; 7: 92-92)

Growth curves for Turkish Girls with Turner Syndrome: Results of the Turkish Turner Syndrome Study Group

(J Clin Res Pediatr Endocrinol 2015; 7: 183-191)

The Role of Thyrotropin-Releasing Hormone Stimulation Test in Management of Hyperthyrotropinemia in Infants

(J Clin Res Pediatr Endocrinol 2015; 7: 211-216)

A Novel Mutation in Human Androgen Receptor Gene Causing Partial Androgen Insensitivity Syndrome in a Patient Presenting with Gynecomastia at Puberty

(J Clin Res Pediatr Endocrinol 2016; 8: 232-235)

A Novel Missense Mutation in HSD17B3 Gene in Two 46,XY Siblings with Female External Gelitalia

(J Clin Res Pediatr Endocrinol 2016; 8: 17-17)

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)

The Relationship between Serum Zonulin Level and Clinical and Laboratory Parameters of Childhood Obesity

(J Clin Res Pediatr Endocrinol 2017; 9: 31-38)
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