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Özen

Samim Özen

Effects of Environmental Endocrine Disruptors on Pubertal Development - Review

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

Renal Anomalies Associated with Ectopic Neurohypophysis - Original Article

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

Clinical Course of Hashimoto's Thyroiditis and Effects of Levothyroxine Therapy on the Clinical Course of the Disease in Children and Adolescents

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

Distribution of Gene Mutations Associated with Familial Normosmic Idiopathic Hypogonadotropic Hypogonadism

(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: -)

Aromatase Deficiency, a Rare Syndrome: Case Report

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

Serum Adiponectin and hsCRP Levels and Non-Invasive Radiological Methods in the Early Diagnosis of Cardiovascular System Complications in Children and Adolescents with Type 1 Diabetes Mellitus

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

Psychiatric Approaches for Disorders of Sex Development: Experience of a Multidisciplinary Team

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

Effects of Carbohydrate Counting Method on Metabolic Control in Children with Type 1 Diabetes Mellitus

(J Clin Res Pediatr Endocrinol 2014; 6: 74-78)

The Impact of Psycho-Educational Training on the Psychosocial Adjustment of Caregivers of Osteogenesis Imperfecta Patients

(J Clin Res Pediatr Endocrinol 2014; 6: 84-92)

Intraoperative Parathyroid Hormone Monitoring Corroborates the Success of Parathyroidectomy in Children

(J Clin Res Pediatr Endocrinol 2014; 6: 158-162)

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

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

A Pediatric Case with Congenital Generalized Lipodystrophy

(J Clin Res Pediatr Endocrinol 2015; 7: 33-33)

The Case of Transient Neonatal Diabetes Mellitus Associated with 6q24

(J Clin Res Pediatr Endocrinol 2015; 7: 48-48)

Genetic Analysis of Lipodystrophies and Recently Found Mutations

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

VDR Gene Analysis of Four Patients with Hereditary 1,25 Dihydroxyvitamin D-Resistant Rickets

(J Clin Res Pediatr Endocrinol 2015; 7: 67-67)

Genotype-Phenotype Correlation of Congenital Adrenal Hyperplasia Cases Having Complex (Multiple) Mutation Detected in CYP21A2 Gene

(J Clin Res Pediatr Endocrinol 2015; 7: 88-88)

Genetic Analysis of Lipodystrophies and Novel Mutations

(J Clin Res Pediatr Endocrinol 2015; 7: 90-90)

Chromosomal Abnormalities in 344 Patients who Were Referred to Cytogenetics Laboratory with Pre-Diagnosis of Short Stature, Turner Syndrome and Sex Developmental Disorders

(J Clin Res Pediatr Endocrinol 2015; 7: 91-91)

Genotype-Phenotype Correlation and Follow-Up Features in Cases with Congenital Hyperinsulinism (CHI)

(J Clin Res Pediatr Endocrinol 2015; 7: 91-91)

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

(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)

Idiopathic Hypogonadotropic Hypogonadism Caused by Inactivating Mutations in SRA1

(J Clin Res Pediatr Endocrinol 2016; 8: 125-134)

Idiopathic Hypogonadotrophic Hypogonadism Caused by Inactivating Mutations in SRA1

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

PTPN11, SOS1, and BRAF Gene Mutation Spectrum in RASopathies in Molecular Diagnosis

(J Clin Res Pediatr Endocrinol 2017; 9: 25-25)

A Novel THRA Gene Mutation in Patient with Thyroid Hormone Resistance

(J Clin Res Pediatr Endocrinol 2017; 9: 29-30)

Six 11-Beta Hydroxylase Deficiency Patients: Identification of Two Novel Mutations

(J Clin Res Pediatr Endocrinol 2017; 9: 26-26)

Investigation of Androgen Receptor Gen Mutation Spectrum in the Turkish Patients with Disorder of Sex Development

(J Clin Res Pediatr Endocrinol 2017; 9: 23-23)

Mutation Spectrum of GCK, HNF1A, and HNF1B in MODY Patients and 40 Novel Mutations

(J Clin Res Pediatr Endocrinol 2017; 9: 22-22)

Persistent Müllerian Duct Syndrome with Transverse Testicular Ectopia: A Novel Anti-Müllerian Hormone Receptor Mutation

(J Clin Res Pediatr Endocrinol 2017; 9: 179-181)

POU1F1 and PROP1 Gene Mutations in 4 Cases of Combined Pituitary Hormone Deficiency

(J Clin Res Pediatr Endocrinol 2017; 9: 20-21)

HOXC4 Gene is Possibly Responsible for Lin-Gettig Syndrome

(J Clin Res Pediatr Endocrinol 2017; 9: 20-20)

A Case Report of Seckel Syndrome

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

Parental View on the Terminology of Disorders of Sex Development

(J Clin Res Pediatr Endocrinol 2017; 9: 1-2)

A Comprehensive Online Calculator for Pediatric Endocrinologists: ÇEDD Çözüm/TPEDS Metrics

(J Clin Res Pediatr Endocrinol 2017; 9: 182-184)

Management of Childhood Thyroid Nodules: Surgical and Endocrinological Findings in a Large Group of Cases

(J Clin Res Pediatr Endocrinol 2017; 9: 222-228)
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