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
Böber

Ece Böber

Growth of Children with Type 1 Diabetes Mellitus - Original Article

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

Fine-Needle Aspiration Biopsy in the Diagnosis and Follow-Up of Thyroid Nodules in Childhood - Original Article

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

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: -)

The Role of Initial Clinical and Laboratory Findings in Infants With Hyperthyrotropinemia to Predict Transient or Permanent Hypothyroidism

(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)

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)

Current Practice in Diagnosis and Treatment of Growth Hormone Deficiency in Childhood: A Survey from Turkey

(J Clin Res Pediatr Endocrinol 2015; 7: 37-44)

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)

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)

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

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

The Missense Alteration A5T of the Thyroid Peroxidase Gene is Pathogenic and Associated with Mild Congenital Hypothyroidism

(J Clin Res Pediatr Endocrinol 2015; 7: 238-241)

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

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

Clinical and Genetic Features of Our Patients with Hypophosphatemic Rickets

(J Clin Res Pediatr Endocrinol 2017; 9: 28-28)

A Novel Mutation in INSR Gene in a Child Presenting with Acanthosis Nigricans

(J Clin Res Pediatr Endocrinol 2017; 9: 17-17)

A Novel De Novo Missense Mutation in HNF4A Resulting in Sulfonylurea-Responsive MODY

(J Clin Res Pediatr Endocrinol 2017; 9: 15-15)

PROP1-Related Combined Pituitary Hormone Deficiency: Case Report

(J Clin Res Pediatr Endocrinol 2017; 9: 12-13)
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