Merih Berberoğlu

Evaluation of Permanent Growth Hormone Deficiency (GHD) in Young Adults with Childhood Onset GHD: A multicenter study - Original Article

(J Clin Res Pediatr Endocrinol 2008; 1: -)

Permanent Central Diabetes Insipidus with Complete Regression of Pituitary Stalk Enlargement After 4 Years of Follow-up - Case Report

(J Clin Res Pediatr Endocrinol 2008; 1: -)

Precocious Puberty and Normal Variant Puberty: Definition, etiology, diagnosis and current management - Review

(J Clin Res Pediatr Endocrinol 2009; 1: 164-174)

Combined Evaluation of IGF-1 and IGFBP-3 as an Index of Efficacy and Safety in Growth Hormone Treated Patients - Original Article

(J Clin Res Pediatr Endocrinol 2009; 1: -)

Vitamin D Deficiency in Turkish Mothers and Their Neonates and in Women of Reproductive Age - Original Article

(J Clin Res Pediatr Endocrinol 2009; 1: -)

Long-Term Follow-Up of a Pseudohypoparathyroidism Type 1A Patient with Missense Mutation (Pro115Ser) in Exon 5 - Case Report

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

Genoa Syndrome and Central Diabetes Insipidus: A Case Report

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

Celiac Disease and Autoimmune Thyroid Disease in Children with Type 1 Diabetes Mellitus: Clinical and HLA-Genotyping Results-Original Article

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

Two Siblings with Isolated GH Deficiency Due to Loss-of-Function Mutation in the GHRHR Gene: Successful Treatment with Growth Hormone Despite Late Admission and Severe Growth Retardation-Case Report

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

Evaluation of Thyroid Functions with Respect to Iodine Status and TRH Test in Chronic Autoimmune Thyroiditis - Original Article

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

Serum IGF-1 and IGFBP-3 Levels in Healthy Children Between 0 and 6 Years of Age - Original Article

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

Two Patients with Partial DiGeorge Syndrome Presenting with Attention Disorder and Learning Difficulties - Case Report

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

Efficiency of Fluid Treatments with Different Sodium Concentration in Children with Type 1 Diabetic Ketoacidosis

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

Synchronous Occurrence of Papillary Carcinoma in the Thyroid Gland and Thyroglossal Duct in an Adolescent with Congenital Hypothyroidism

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

Distribution of Gene Mutations Associated with Familial Normosmic Idiopathic Hypogonadotropic Hypogonadism

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

Relationships Between Osteocalcin, Glucose Metabolism and Adiponectin in Obese Children: Is there Crosstalk Between Bone Tissue and Glucose Metabolism?

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

Syndromic Disorders with Short Stature

(J Clin Res Pediatr Endocrinol 2014; 6: 1-8)

ROHHAD Syndrome: Reasons for Diagnostic Difficulties in Obesity

(J Clin Res Pediatr Endocrinol 2014; 6: 254-257)

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)

A Deep Intronic HADH Splicing Mutation (c.636+471G>T) in a Congenital Hyperinsulinemic Hypoglycemia Case: Long Term Clinical Course

(J Clin Res Pediatr Endocrinol 2015; 7: 144-147)

Difficulties in the Clinical Approach to Disorders of Sexual Development: Role of the Genes in the Approach

(J Clin Res Pediatr Endocrinol 2015; 7: 31-31)

Tamoxifen Treatment for Pubertal Gynecomastia in a Patient with Partial Androgen Insensitivity Syndrome

(J Clin Res Pediatr Endocrinol 2015; 7: 76-76)

The Effect of Recombinant Growth Hormone Treatment in Children with Idiopathic Short Stature and Low Insulin-Like Growth Factor-1 Levels

(J Clin Res Pediatr Endocrinol 2015; 7: 301-306)

Investigation of SHOX Gene Mutations in Turkish Patients with Idiopathic Short Stature

(J Clin Res Pediatr Endocrinol 2016; 8: 144-149)

Gonadotropin-Releasing Hormone Analogue Treatment in Females with Moderately Early Puberty: No Effect on Final Height

(J Clin Res Pediatr Endocrinol 2016; 8: 211-217)

Regulatory T Cells and Vitamin D Status in Children with Chronic Autoimmune Thyroiditis

(J Clin Res Pediatr Endocrinol 2016; 8: 276-281)

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)

Current Status of Childhood Hyperinsulinemic Hypoglycemia in Turkey

(J Clin Res Pediatr Endocrinol 2016; 8: 375-380)

Delayed Diagnosis of a 17-Hydroxylase/17,20-Lyase Deficient Patient Presenting as a 46,XY Female: A Low Normal Potassium Level Can Be an Alerting Diagnostic Sign

(J Clin Res Pediatr Endocrinol 2017; 9: 163-167)

Response to Anastrozole Treatment in a Case with Peutz-Jeghers Syndrome and a Large Cell Calcifying Sertoli Cell Tumor

(J Clin Res Pediatr Endocrinol 2017; 9: 168-171)
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