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Savaş Erdeve

Şenay Savaş Erdeve

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: -)

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: -)

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: -)

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: -)

Hyperinsulinemic Hypoglycemia: Experience in A Series of 17 Cases

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

Familial Partial Lipodystrophy Linked to aNovel Peroxisome Proliferator-Activated Receptor -γ (PPARG) Mutation, H449L

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

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)

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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