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
Daar

Ghaniya Daar

Fetal Adrenal Suppression Due to Maternal Corticosteroid Use: Case Report

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

Congenital Hypothyroidism Due To Maternal Radioactive Iodine Exposure During Pregnancy

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

Unusual Course of Congenital Hypothyroidism and Route of the L-Thyroxine Treatment in a Preterm Newborn

(J Clin Res Pediatr Endocrinol 2014; 6: 177-179)
Dağdeviren Çakır

Aydilek Dağdeviren Çakır

A Novel Mutation in AMHR2 Gene in Two Siblings with Persistent Müllerian Duct Syndrome

(J Clin Res Pediatr Endocrinol 2017; 9: 19-19)
Dahl

Maria Dahl

Subclinical Hypothyroidism in Danish Lean and Obese Children and Adolescents

(J Clin Res Pediatr Endocrinol 2017; 9: 8-16)
Dalabih

Abdallah Dalabih

Variability of DKA Management Among Pediatric Emergency Room and Critical Care Providers: A Call for More Evidence-Based and Cost-Effective Care?

(J Clin Res Pediatr Endocrinol 2014; 6: 190-191)
Dallar

Yıldız Dallar

A Novel Pathogenic DNA Variation in the OCRL1 Gene in Lowe Syndrome - Case Report

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

Increased Thrombin-Activatable Fibrinolysis Inhibitor and Decreased Tissue Factor Pathway Inhibitor and Thrombomodulin Levels in Children with Hypothyroidism

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

Prevalence of Obesity and Associated Risk Factors Among Adolescents in Ankara, Turkey

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

Çağrı Damar

Soluble Endoglin Level Increase Occurs Prior to Development of Subclinical Structural Vascular Alterations in Diabetic Adolescents

(J Clin Res Pediatr Endocrinol 2016; 8: 313-320)
Danda

Sumita Danda

Patient with Mutation in the Matrix Metalloproteinase 2 (MMP2) Gene - A Case Report and Review of the Literature

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

Waleed Dandan

A Newly-Discovered Mutation in the RFX6 Gene of the Rare Mitchell-Riley Syndrome

(J Clin Res Pediatr Endocrinol 2016; 8: 246-249)
Darbro

Benjamin Darbro

Uniparental Isodisomy of Chromosome 1 Unmasking an Autosomal Recessive 3-Beta Hydroxysteroid Dehydrogenase Type II-Related Congenital Adrenal Hyperplasia

(J Clin Res Pediatr Endocrinol 2017; 9: 70-73)
Darcan

Şükran Darcan

A Randomized Clinical Trial Comparing Breakfast and Bedtime Administration of Insulin Glargine in Children and Adolescents with Type 1 Diabetes - Original Article

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

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: -)

Ghrelin Levels in Children with Constitutional Delay of Growth and Puberty - Original Article

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

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: -)

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: -)

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: -)

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)

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)

Melanocortin-4 Receptor Mutation and Obesity

(J Clin Res Pediatr Endocrinol 2015; 7: 43-43)

The Case of Transient Neonatal Diabetes Mellitus Associated with 6q24

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

A Case of Polyglandular Autoimmune Syndrome Type One with Hypercalcemia and Hypotension

(J Clin Res Pediatr Endocrinol 2015; 7: 51-51)

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)

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)

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)

Editorial

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

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)

Anthropometric Measurements and Complications of Achondroplasia Patients

(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)

Parental View on the Terminology of Disorders of Sex Development

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

Feyza Darendeliler

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: -)

Foreword

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

Puberty and Pubertal Growth in Healthy Turkish Girls: No evidence for secular trend - Original Article

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

Severe Short Stature: an unusual finding in lipoid proteinosis - Case Report

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

Safety of Growth Hormone Treatment

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

CYP21A2 Gene Mutations in Congenital Adrenal Hyperplasia: Genotype-phenotype correlation in Turkish children - Original Article

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

A Patient with 22q11.2 Deletion Syndrome: case report - Case Report

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

Effect Of Hypo-and Euthyroid Status On Serum Cystatin C Levels-Original Article

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

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: -)

The Distribution of Exon 3-Deleted/Full-Length Growth Hormone Receptor Polymorphism in the Turkish Population

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

Permanent Neonatal Diabetes Mellitus: Same Mutation, Different Glycemic Control with Sulfonylurea Therapy on Long-Term Follow-up

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

Is Premature Thelarche in the First Two Years of Life Transient?

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

Clinical and Laboratory Characteristics of Children Referred for Early Puberty: Preponderance in 7-8 Years of Age

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

Growth Hormone/Insulin-Like Growth Factor-1 
Axis as Related to Body Mass Index in Patients with Idiopathic Short Stature

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

Z-Score Reference Values for Height in Turkish Children Aged 6 to 18 Years

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

Long-term Endocrine Evaluation of Childhood Brain Tumors

(J Clin Res Pediatr Endocrinol 2015; 7: 22-22)

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

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

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)

Epidemiologic Features of Type 1 Diabetic Patients between 0 and 18 Years of Age in İstanbul City

(J Clin Res Pediatr Endocrinol 2015; 7: 49-56)

Central Precocious Puberty in a Patient with Multiple Pituitary Hormone Deficiency Due to POU1F1 (PIT1) Gene Mutation

(J Clin Res Pediatr Endocrinol 2015; 7: 72-72)

Multiple Pituitary Hormone Deficiency Associated with Pituitary Hyperplasia: A Case Report

(J Clin Res Pediatr Endocrinol 2015; 7: 81-81)

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)

Reference Values for Weight, Height, Head Circumference, and Body Mass Index in Turkish Children

(J Clin Res Pediatr Endocrinol 2015; 7: 280-293)

Editor’s Note

(J Clin Res Pediatr Endocrinol 2016; 8: 0-0)

Anti-Müllerian Hormone and Inhibin-A, but not Inhibin-B or Insulin-Like Peptide-3, may be Used as Surrogates in the Diagnosis of Polycystic Ovary Syndrome in Adolescents: Preliminary Results

(J Clin Res Pediatr Endocrinol 2016; 8: 288-297)

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 Critical Appraisal of Growth Hormone Therapy in Growth Hormone Deficiency and Turner Syndrome Patients in Turkey

(J Clin Res Pediatr Endocrinol 2016; 8: 490-495)

Four 46,XY DSD Cases with Novel Mutations in AR and SRD5A2 Genes

(J Clin Res Pediatr Endocrinol 2017; 9: 24-24)

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

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

Dhanjit Kumar Das

Identification of Novel Mutations in STAR Gene in Patients with Lipoid Congenital Adrenal Hyperplasia: A First Report from India

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

Primary Hyperparathyroidism Masquerading as Rickets: Diagnostic Challenge and Treatment Outcomes

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

Saumik Datta

Primary Hyperparathyroidism Masquerading as Rickets: Diagnostic Challenge and Treatment Outcomes

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

Raphael David

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

Evaluation of Adolescents for Polycystic Ovary Syndrome in an Urban Population - Original Article

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

Elisa De Franco

A Diabetic Infant with Homozygous LRBA Mutation: The Youngest Patient Reported

(J Clin Res Pediatr Endocrinol 2016; 8: 16-16)

Hyperinsulinemic Hypoglycemia Due to Homozygous C.706 C>T (P. R236X) Mutation in 3 Siblings: Presentation with Resistant Epilepsy

(J Clin Res Pediatr Endocrinol 2017; 9: 29-29)
De Freitas Mathias

Paulo Cezar De Freitas Mathias

Environmental Contaminants and Pancreatic Beta-Cells

(J Clin Res Pediatr Endocrinol 2016; 8: 257-263)
de la O. Cavazos

Manuel E. de la O. Cavazos

Adding Multiple Adipokines into the Model do not Improve Weight Gain Prediction by Leptin Levels in Newborns

(J Clin Res Pediatr Endocrinol 2016; 8: 321-324)
Deda

Gülhiz Deda

Genoa Syndrome and Central Diabetes Insipidus: A Case Report

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

Asma Deeb

Phenotype, Sex of Rearing, Gender Re-Assignment, and Response to Medical Treatment in Extended Family Members with a Novel Mutation in the SRD5A2 Gene

(J Clin Res Pediatr Endocrinol 2016; 8: 236-240)
Değirmenci

Serpil Değirmenci

Critical Points in the Management of Pseudohypoaldosteronism Type 1 - Case Report

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

Ehsan Dehghan

SLC34A3 Intronic Deletion in a New Kindred with Hereditary Hypophosphatemic Rickets with Hypercalciuria

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

Prapai Dejkhamron

Radioactive Iodine for Thyrotoxicosis in Childhood and Adolescence: Treatment and Outcomes

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

Kenan Delil

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

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

Assoc. Prof. Dr. Korcan Demir

Editorial

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

Hepatic Glycogenosis in a Patient with Type 1 Diabetes: Mauriac Syndrome vs. Congenital Glycogen Storage Disease

(J Clin Res Pediatr Endocrinol 2017; 9: 16-16)

Mitochondrial ATPase Subunit 6 and Cytochrome B Gene Variations in Obese Turkish Children

(J Clin Res Pediatr Endocrinol 2014; 6: 209-215)

Epidemiologic Features of Type 1 Diabetic Patients between 0 and 18 Years of Age in İstanbul City

(J Clin Res Pediatr Endocrinol 2015; 7: 49-56)

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

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

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: -)

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: -)

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: -)

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

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

Importance of Insulin Immunoassays in the Diagnosis of Factitious Hypoglycemia

(J Clin Res Pediatr Endocrinol 2014; 6: 258-261)

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

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

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)

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)

46,XY Complete Gonadal Dysgenesis: A Case Report

(J Clin Res Pediatr Endocrinol 2015; 7: 65-65)

Genetic Diagnosis Using Whole Exome Analysis in Two Cases with Malignant Infantile Osteopetrosis

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

A Case with Infantile-Onset Pancytopenia and Hyperglycemia Associated with SLC19A2 Mutation

(J Clin Res Pediatr Endocrinol 2015; 7: 89-89)

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)

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)

Genetic Diagnosis Using Whole Exome Analysis in Two Cases with Malignant Osteopetrosis of Infancy

(J Clin Res Pediatr Endocrinol 2015; 7: 356-357)

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)

Higher-Than-Conventional Subcutaneous Regular Insulin Doses in Diabetic Ketoacidosis in Children and Adolescents

(J Clin Res Pediatr Endocrinol 2017; 9: 132-137)

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)

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

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

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

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

Genetic Analysis of Lipodystrophies and Recently Found Mutations

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

Genetic Analysis of Lipodystrophies and Novel Mutations

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

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

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

Atypical LMNA Mutation in EXON 11 Associated with a Milder Clinical Outcome in Dunnigan-Type Familial Partial Lipodystrophy

(J Clin Res Pediatr Endocrinol 2017; 9: 19-19)

Association of Subclinical Hypothyroidism with Dyslipidemia and Increased Carotid Intima-Media Thickness in Children

(J Clin Res Pediatr Endocrinol 2017; 9: 144-149)
Demirağ

Mehmet Derya Demirağ

A Rare Genodermatosis: H Syndrome

(J Clin Res Pediatr Endocrinol 2017; 9: 10-10)
Demiral

Meliha Demiral

Gonadoblastoma and Papillary Tubal Hyperplasia in Ovotesticular Disorder of Sexual Development

(J Clin Res Pediatr Endocrinol 2016; 8: 351-355)
Demiral Sezer

Sibel Demiral Sezer

Hepatic Glycogenosis in a Patient with Type 1 Diabetes: Mauriac Syndrome vs. Congenital Glycogen Storage Disease

(J Clin Res Pediatr Endocrinol 2017; 9: 16-16)
Demirbaş

Özgecan Demirbaş

A Rare Cause of Insulin-Dependent Diabetes: Two Siblings with Walcott-Rallison Syndrome

(J Clin Res Pediatr Endocrinol 2017; 9: 6-7)
Demirbilek

Hüseyin Demirbilek

GnRH Stimulation Test in Precocious Puberty: Single Sample is Adequate for Diagnosis and Dose Adjustment - Original Article

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

Hypophosphatasia Presenting with Pyridoxine-Responsive Seizures, Hypercalcemia, and Pseudotumor Cerebri: Case Report

(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: -)

Incidence of Type 1 Diabetes Mellitus in Turkish Children from the Southeastern Region of the Country: A Regional Report

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

Multiple Pituitary Hormone Deficiency Due to Gunshot Injury in a 6-Year-Old Girl

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

Prepubertal Unilateral Gynecomastia: Report of 2 Cases

(J Clin Res Pediatr Endocrinol 2014; 6: 250-253)

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

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

Capillary Bedside Blood Glucose Measurement in Neonates: Missing a Diagnosis of Galactosemia

(J Clin Res Pediatr Endocrinol 2015; 7: 83-85)

Severe Congenital Insulin Resistance Syndrome Due to a Compound Heterozygous c.836G>A & c.1268+2T>A Mutation in Insulin Receptor (INSR) Gene

(J Clin Res Pediatr Endocrinol 2015; 7: 85-85)

Efficacy and Safety of Sirolimus (mTOR Inhibitor) in Two Patients with Diazoxide-Unresponsive Hyperinsulinemic Hypoglycemia

(J Clin Res Pediatr Endocrinol 2015; 7: 86-86)

Successful Transfer from Insulin to Oral Sulphonylurea in an Infant and His Mother with Monogenic Diabetes Due to a Heterozygous Missense Mutation in the ABCC8 Gene

(J Clin Res Pediatr Endocrinol 2015; 7: 86-86)

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)

Bone Mineral Density in Adolescent Girls with Hypogonadotropic and Hypergonadotropic Hypogonadism

(J Clin Res Pediatr Endocrinol 2016; 8: 163-169)

Hyperinsulinemic Hypoglycemia Due to Homozygous C.706 C>T (P. R236X) Mutation in 3 Siblings: Presentation with Resistant Epilepsy

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

Korcan Demircan Sezer

A Case with Acrodysostosis and Hormone Resistance

(J Clin Res Pediatr Endocrinol 2015; 7: 75-75)
Demirci

Serpil Demirci

The Effects of Six-Month L-Thyroxine Treatment on Cognitive Functions and Event-Related Brain Potentials in Children with Subclinical Hypothyroidism

(J Clin Res Pediatr Endocrinol 2015; 7: 102-108)
Demircioğlu Kılıç

Beltinge Demircioğlu Kılıç

Autoimmune Polyglandular Syndrome Type 3c with Ectodermal Dysplasia, Immune Deficiency and Hemolytic-Uremic Syndrome

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

Atalay Demirel

Hidden Toxicity in Neonatal Intensive Care Units: Phthalate Exposure in Very Low Birth Weight Infants

(J Clin Res Pediatr Endocrinol 2016; 8: 298-304)

Maternal and Neonatal Urinary Iodine Status and its Effect on Neonatal TSH Levels in a Mildly Iodine-Deficient Area

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

Microvascular Complications in Adolescents with Type 1 Diabetes Mellitus

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

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

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

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)

Prevalence of Dyslipidemia and Associated Factors in Obese Children and Adolescents

(J Clin Res Pediatr Endocrinol 2015; 7: 228-234)

A Novel Homozygous Mutation in the KCNJ11 Gene of a Neonate with Congenital Hyperinsulinism and Successful Management with Sirolimus

(J Clin Res Pediatr Endocrinol 2016; 8: 478-481)

A Case Presentation: Sleeve Gastrectomy with Transit Bipartition as a Treatment of Type 2 Diabetes Mellitus Applied for the First Time to a Bulgarian Citizen

(J Clin Res Pediatr Endocrinol 2017; 9: 6-6)
Demirkan

Bora Demirkan

Investigation of BRAF Hotspot Mutations in Papillary Thyroid Tumor Samples

(J Clin Res Pediatr Endocrinol 2015; 7: 68-68)
Demirkaya

Metin Demirkaya

A Rare Cause of Precocious Puberty: Hepatoblastoma - Case Report

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

Thyroid Functions in Long-Term Survivors of Pediatric Hodgkin’s Lymphoma Treated with Chemotherapy and Radiotherapy - Original Article

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

Nafiye Demirkıran Urgancı

Autoimmune Polyglandular Syndrome Type 2: A Rare Condition in Childhood

(J Clin Res Pediatr Endocrinol 2015; 7: 80-82)
Demirpençe

Savaş Demirpençe

Cardiac Function in Newborns with Congenital Hypothyroidism: Association with Thyroid-Stimulating Hormone Levels

(J Clin Res Pediatr Endocrinol 2015; 7: 307-311)
Demirtaş

Şafak Demirtaş

Dermal and Ophthalmic Findings in Pseudohypoaldosteronism

(J Clin Res Pediatr Endocrinol 2015; 7: 155-158)

Weight for Length/Height Percentiles in Infants and Young Children in Kayseri/Turkey

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

You-Ping Deng

Low-Grade Inflammation and Increased Arterial Stiffness in Chinese Youth and Adolescents with Newly-Diagnosed Type 2 Diabetes Mellitus

(J Clin Res Pediatr Endocrinol 2015; 7: 268-273)
Deniz

Ahmet Deniz

Capillary Bedside Blood Glucose Measurement in Neonates: Missing a Diagnosis of Galactosemia

(J Clin Res Pediatr Endocrinol 2015; 7: 83-85)

A Case of Thyroid Hormone Resistance

(J Clin Res Pediatr Endocrinol 2015; 7: 75-75)
Derinkuyu

Betül Derinkuyu

Soluble Endoglin Level Increase Occurs Prior to Development of Subclinical Structural Vascular Alterations in Diabetic Adolescents

(J Clin Res Pediatr Endocrinol 2016; 8: 313-320)
Derinöz

Okşan Derinöz

Age-Specific Frequencies and Characteristics of Ovarian Cysts in Children and Adolescents

(J Clin Res Pediatr Endocrinol 2017; 9: 58-62)
Didi

Mohammed Didi

Fluoxetine-Induced Hypoglycaemia in a Patient with Congenital Hyperinsulinism on Lanreotide Therapy

(J Clin Res Pediatr Endocrinol 2016; 8: 347-350)
Dilli

Dilek Dilli

The Role of Interleukin-6 and C-Reactive Protein in Non-Thyroidal Illness in Premature Infants Followed in Neonatal Intensive Care Unit

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

Establishment and Development of a National Newborn Screening Programme for Congenital Hypothyroidism in Turkey

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

Uğur Dilmen

The Role of Interleukin-6 and C-Reactive Protein in Non-Thyroidal Illness in Premature Infants Followed in Neonatal Intensive Care Unit

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

Establishment and Development of a National Newborn Screening Programme for Congenital Hypothyroidism in Turkey

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

Halit Diri

Osteogenesis Imperfecta: Case Report

(J Clin Res Pediatr Endocrinol 2017; 9: 11-11)
Dissanayake

Vajira H.W. Dissanayake

An Infant Born to a Mother with Gestational Diabetes Presenting with 49,XXXXY Syndrome and Renal Agenesis-A Case Report

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

Emre Divarcı

Intraoperative Parathyroid Hormone Monitoring Corroborates the Success of Parathyroidectomy in Children

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

Ceyhun Dizdarer

Hypochondroplasia in a Child with 1620C>G (Asn540Lys) Mutation in FGFR3

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

Impact of Insulin Resistance on Insulin-Like Growth Factor-1/Insulin Like Growth Factor-Binding Protein-3 Axis and on Early Weight Gain in Small for Gestational Age Infants

(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: -)

Neonatal Seizure as a Manifestation of Unrecognized Maternal Hyperparathyroidism

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

Maja Djordjevic

Early Presentation of Hyperinsulinism/Hyperammonemia Syndrome in Three Serbian Patients

(J Clin Res Pediatr Endocrinol 2016; 8: 228-231)
Doğan

Canan Doğan

Hidden Toxicity in Neonatal Intensive Care Units: Phthalate Exposure in Very Low Birth Weight Infants

(J Clin Res Pediatr Endocrinol 2016; 8: 298-304)

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

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

An Obese Case with Homozygous Leptin Receptor Mutation

(J Clin Res Pediatr Endocrinol 2015; 7: 60-60)

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)

Vitamin D Deficiency in Children and Adolescents

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

Effect of Cytokine Signaling 3 Gene Polymorphisms in Childhood Obesity

(J Clin Res Pediatr Endocrinol 2016; 8: 452-460)

The Effects of Six-Month L-Thyroxine Treatment on Cognitive Functions and Event-Related Brain Potentials in Children with Subclinical Hypothyroidism

(J Clin Res Pediatr Endocrinol 2015; 7: 102-108)

Prevalence of Overweight and Obesity in Children and Adolescents in Eastern Turkey-Original Article

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

Distribution of Gene Mutations Associated with Familial Normosmic Idiopathic Hypogonadotropic Hypogonadism

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

One Base Deletion (c.2422delT) in the TPO Gene Causes Severe Congenital Hypothyroidism

(J Clin Res Pediatr Endocrinol 2014; 6: 169-173)

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

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

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)

A Homozygous Nonsense Thyroid Peroxidase Mutation (R540X) Consistently Causes Congenital Hypothyroidism in Two Siblings Born to a Consanguineous Family

(J Clin Res Pediatr Endocrinol 2015; 7: 323-328)

Pseudohypoparathyroisidm Type 1a: A Case Report

(J Clin Res Pediatr Endocrinol 2016; 8: 15-15)

Relationship between Neck Circumference and Non-Alcoholic Fatty Liver Disease in Childhood Obesity

(J Clin Res Pediatr Endocrinol 2016; 8: 32-39)
Doğru

Esra Doğru

The Role of Active Video-Accompanied Exercises in Improvement of the Obese State in Children: A Prospective Study from Turkey

(J Clin Res Pediatr Endocrinol 2016; 8: 334-340)

A Rare Genetic Disorder: Partial Trisomy on Chromosome 21

(J Clin Res Pediatr Endocrinol 2015; 7: 78-78)
Doğu

Figen Doğu

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

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

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

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

Önder Doksöz

Cardiac Function in Newborns with Congenital Hypothyroidism: Association with Thyroid-Stimulating Hormone Levels

(J Clin Res Pediatr Endocrinol 2015; 7: 307-311)
Dokurel

İpek Dokurel

Primary Adrenal Insufficiency Caused by a Novel Mutation in DAX1 Gene

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

Susanne Dold

Breast-Milk Iodine Concentrations, Iodine Status, and Thyroid Function of Breastfed Infants Aged 2-4 Months and Their Mothers Residing in a South African Township

(J Clin Res Pediatr Endocrinol 2016; 8: 381-391)
Donaldson

Malcolm Donaldson

Diagnostic Use of Skeletal Survey in Suspected Skeletal Dysplasia - Original Article

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

Optimising Outcome in Congenital Hypothyroidism; Current Opinions on Best Practice in Initial Assessment and Subsequent Management

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

Fatemeh Dorreh

Epidemiology of Congenital Hypothyroidism in Markazi Province, Iran

(J Clin Res Pediatr Endocrinol 2014; 6: 105-110)
Dougan

Elizabeth Dougan

Diagnostic Use of Skeletal Survey in Suspected Skeletal Dysplasia - Original Article

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

Marzieh Rostami Dovom

Menarcheal Age and Risk of Type 2 Diabetes: A Community-Based Cohort Study

(J Clin Res Pediatr Endocrinol 2017; 9: 156-162)
Döğer

Esra Döğer

Cardio-Facio-Cutaneous Syndrome with Precocious Puberty, Growth Hormone Deficiency and Hyperprolactinemia

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

Extensive Middle Cranial Fossa Arachnoid Cysts and Different Clinical Presentation in Two Patients

(J Clin Res Pediatr Endocrinol 2014; 6: 174-176)

A Hypogonadotropic Hypogonadism Case as a Consequence of GNRHR Mutation

(J Clin Res Pediatr Endocrinol 2015; 7: 56-56)

Gonadoblastoma with Dysgerminoma in a Phenotypically Turner-Like Girl with 45,X/46,XY Karyotype

(J Clin Res Pediatr Endocrinol 2015; 7: 336-339)

Soluble Endoglin Level Increase Occurs Prior to Development of Subclinical Structural Vascular Alterations in Diabetic Adolescents

(J Clin Res Pediatr Endocrinol 2016; 8: 313-320)

Thyroid Hormone Resistance P453A Mutation

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

Zafer Dökümcü

Intraoperative Parathyroid Hormone Monitoring Corroborates the Success of Parathyroidectomy in Children

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

Hakan Döneray

The Effect of Vitamin D Treatment on Serum Adiponectin Levels in Children with Vitamin D Deficiency Rickets - Original Article

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

Circulating Insulin-like Growth Factor Binding Protein-4 (IGFBP-4) is not Regulated by Parathyroid Hormone and Vitamin D in vivo: Evidence from Children with Rickets - Original Article

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

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

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

The First Turkish Case of Hypoparathyroidism, Deafness and Renal Dysplasia (HDR) Syndrome

(J Clin Res Pediatr Endocrinol 2015; 7: 140-143)

Hypoparathyroidism-Deafness-Renal Disease Syndrome: The First Case Report from Turkey

(J Clin Res Pediatr Endocrinol 2015; 7: 73-73)

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)

Plasma Kisspeptin Levels in Newborn Infants with Breast Enlargement

(J Clin Res Pediatr Endocrinol 2015; 7: 192-196)
Dönmez

Ayşe Sena Dönmez

The First Turkish Case of Hypoparathyroidism, Deafness and Renal Dysplasia (HDR) Syndrome

(J Clin Res Pediatr Endocrinol 2015; 7: 140-143)

Hypoparathyroidism-Deafness-Renal Disease Syndrome: The First Case Report from Turkey

(J Clin Res Pediatr Endocrinol 2015; 7: 73-73)
Duman

Fatma Duman

The Role of Active Video-Accompanied Exercises in Improvement of the Obese State in Children: A Prospective Study from Turkey

(J Clin Res Pediatr Endocrinol 2016; 8: 334-340)
Duncan

Roderick Duncan

Diagnostic Use of Skeletal Survey in Suspected Skeletal Dysplasia - Original Article

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

Tuğba Durakoğlugil

Investigation of Association Between Paraoxonase-1 L55M (RS854560) and Q192R (RS662) Polymorphisms and Potential Atherosclerotic Risk Factors in PCOS Patients

(J Clin Res Pediatr Endocrinol 2017; 9: 27-27)
Durmaz

Asude Durmaz

Prevalence and Molecular Characteristics of Y Chromosome Microdeletions in Infertile Males: A Single-Center Study

(J Clin Res Pediatr Endocrinol 2015; 7: 74-74)

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

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

A Novel HESX1 Mutation in a Case with Panhypopituitarism

(J Clin Res Pediatr Endocrinol 2017; 9: 23-24)

Anthropometric Measurements and Complications of Achondroplasia Patients

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

The Mutation Spectrum of DHCR7 Gene and Two Novel Mutations

(J Clin Res Pediatr Endocrinol 2017; 9: 21-22)

FGFR2 Gene Mutations in Patients with Syndromic or Isolated Craniosynostosis

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

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

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

Prevalence and Molecular Characteristics of Y Chromosome Microdeletions in Infertile Males: A Single-Center Study

(J Clin Res Pediatr Endocrinol 2015; 7: 74-74)

A Case of Pycnodysostosis with Bilateral Choanal Atresia

(J Clin Res Pediatr Endocrinol 2015; 7: 70-70)

Urinary Bisphenol A Levels in Girls with Idiopathic Central Precocious Puberty

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

A Combination of Nifedipine and Octreotide Treatment in an Hyperinsulinemic Hypoglycemic Infant

(J Clin Res Pediatr Endocrinol 2014; 6: 119-121)

A Novel Null Mutation in P450 Aromatase Gene (CYP19A1) Associated with Development of Hypoplastic Ovaries in Humans

(J Clin Res Pediatr Endocrinol 2016; 8: 205-210)

Hypogonadotropic Hypogonadism due to Novel FGFR1 Mutations

(J Clin Res Pediatr Endocrinol 2017; 9: 95-100)
Durmuş

Mehmet Sait Durmuş

Clinical and Laboratory Characteristics of Children Referred for Early Puberty: Preponderance in 7-8 Years of Age

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

Fatma Dursun

Developmental Defects of the Thyroid Gland: Relationship with Advanced Maternal Age

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

Remission with Cabergoline in Adolescent Boys with Cushing’s Disease

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

Atypical Presentation of Hashimoto’s Disease in an Adolescent: Thyroid-Associated Ophthalmopathy

(J Clin Res Pediatr Endocrinol 2014; 6: 262-265)

Assessment of Anti-Müllerian Hormone Level in Management of Adolescents with Polycystic Ovary Syndrome

(J Clin Res Pediatr Endocrinol 2016; 8: 55-60)

A Novel Missense Mutation in the CLPP Gene Causing Perrault Syndrome Type 3 in a Turkish Family

(J Clin Res Pediatr Endocrinol 2016; 8: 472-477)
Dutta

Deep Dutta

Iatrogenic Cushing’s Syndrome Following Short-Term Intranasal Steroid Use

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

Isolated Cushing’s Syndrome in Early Infancy Due to Left Adrenal Adenoma: An Unusual Aetiology

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

Syndrome of Extreme Insulin Resistance 
(Rabson-Mendenhall Phenotype) with Atrial Septal Defect: Clinical Presentation and Treatment Outcomes

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

Medical Management of Thyroid Ectopia: Report of Three Cases

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

Primary Hyperparathyroidism Masquerading as Rickets: Diagnostic Challenge and Treatment Outcomes

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

Bumin Dündar

Prevalence of Metabolic Syndrome in Obese Children and Adolescents using Three Different Criteria and Evaluation of Risk Factors - Original Article

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

Diabetic Ketoacidosis Presenting with Pseudonormoglycemia in a 15-Year-Old Girl with Type 1 Diabetes Mellitus

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

Relationship Between Aspartate Aminotransferase-to-Platelet Ratio Index and Carotid Intima-Media Thickness in Obese Adolescents with Non-Alcoholic Fatty Liver Disease

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

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

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

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)

Social Anxiety, Depression and Self-Esteem in Obese Adolescent Girls with Acanthosis Nigricans

(J Clin Res Pediatr Endocrinol 2015; 7: 63-68)

The Effects of Six-Month L-Thyroxine Treatment on Cognitive Functions and Event-Related Brain Potentials in Children with Subclinical Hypothyroidism

(J Clin Res Pediatr Endocrinol 2015; 7: 102-108)

Long-Term Treatment with n-3 Polyunsaturated Fatty Acids as a Monotherapy in Children with Nonalcoholic Fatty Liver Disease

(J Clin Res Pediatr Endocrinol 2015; 7: 121-127)

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)

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)

Clinical and Genetic Features of Our Patients with Hypophosphatemic Rickets

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

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

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

Comparison of the Efficacy and Safety of Insulin Glargine and Insulin Detemir with NPH Insulin in Children and Adolescents with Type 1 Diabetes Mellitus Receiving Intensive Insulin Therapy - Original Article

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

Vanishing Testes: A Literature Review

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

Association Between Insulin Resistance and 
Oxidative Stress Parameters in Obese Adolescents with Non-Alcoholic Fatty Liver Disease

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

Adipokines in Breast Milk: An Update

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

Novel Growth Hormone-Releasing Hormone Receptor Gene Mutations in Turkish Children with Isolated Growth Hormone Deficiency

(J Clin Res Pediatr Endocrinol 2014; 6: 202-208)

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

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

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)

Can Stoss Therapy Be Used in Children with Vitamin D Deficiency or Insufficiency without Rickets?

(J Clin Res Pediatr Endocrinol 2017; 9: 150-155)

The Effectiveness of Cinacalcet as an Adjunctive Therapy for Hereditary 1,25 Dihydroxyvitamin D3-Resistant Rickets

(J Clin Res Pediatr Endocrinol 2017; 9: 172-178)

The Mutation Spectrum of DHCR7 Gene and Two Novel Mutations

(J Clin Res Pediatr Endocrinol 2017; 9: 21-22)

Comparison of the Efficacy and Safety of Insulin Glargine and Insulin Detemir with NPH Insulin in Children and Adolescents with Type 1 Diabetes Mellitus Receiving Intensive Insulin Therapy - Original Article

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

Prevalence of Metabolic Syndrome in Obese Children and Adolescents using Three Different Criteria and Evaluation of Risk Factors - Original Article

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

The Effects of Six-Month L-Thyroxine Treatment on Cognitive Functions and Event-Related Brain Potentials in Children with Subclinical Hypothyroidism

(J Clin Res Pediatr Endocrinol 2015; 7: 102-108)
Dündaröz

Ruşen Dündaröz

Cardiac Autonomic Functions in Obese Children - Original Article

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

Correlation of Brain Neuropeptide (Nesfatin-1 and Orexin-A) Concentrations with Anthropometric and Biochemical Parameters in Malnourished Children

(J Clin Res Pediatr Endocrinol 2015; 7: 197-202)
Düzova

Ali Düzova

A Rare Case of Neonatal Diabetes due to COQ2 Gene Mutation

(J Clin Res Pediatr Endocrinol 2015; 7: 16-16)
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