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
Baban

Melis Baban

Food Types in the Diet and the Nutrient Intake of Obese and Non-Obese Children - Original Article

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

Sofia Babay

H Syndrome: A Rare Monogenic Cause of Insulin-Dependent Diabetes Mellitus

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

H. Ömür Babayiğit

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)
Babu

Shiny Babu

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: -)
Bacak

Gökhan Bacak

Prepubertal Unilateral Gynecomastia: Report of 2 Cases

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

Franco Bagnoli

Thyroid Function in Small for Gestational Age Newborns: A Review

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

Özlem Bağ

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

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

Nerin Bahçeciler Önder

The Role of Adenovirus Serotype 36 in Childhood Obesity

(J Clin Res Pediatr Endocrinol 2017; 9: 3-3)
Bahreynian

Maryam Bahreynian

Association between Obesity and Parental Weight Status in Children and Adolescents

(J Clin Res Pediatr Endocrinol 2017; 9: 111-117)
Bal

Cengiz Bal

Cellular Trace Element Changes in Type 1 Diabetes Patients

(J Clin Res Pediatr Endocrinol 2016; 8: 180-186)

Current Loss-of-Function Mutations in the Thyrotropin Receptor Gene: When to Investigate, Clinical Effects, and Treatment

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

Keziban Aslı Bala

Pseudohypoparathyroisidm Type 1a: A Case Report

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

Mine Balasar

A Case of Mosaic 45,X/46,XY Infertile Man with an AZF Deletion

(J Clin Res Pediatr Endocrinol 2015; 7: 77-77)

Gene Conversion and Congenital Adrenal Hyperplasia: Two Case Reports

(J Clin Res Pediatr Endocrinol 2017; 9: 4-4)

A Case of Mosaic 45,X/46,XY Infertile Man with an AZF Deletion

(J Clin Res Pediatr Endocrinol 2015; 7: 77-77)
Balat

Ayşe Balat

Trends in the Frequency of HLA DR-DQ Haplotypes Among Children and Adolescents with Type 1 Diabetes Mellitus in the Southeast Region of Turkey

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

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

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

The Possible Role of Mitochondrial Uncoupling Protein 2 (UCP2) Gene on the Development of Metabolic Syndrome and Platelet Count in Obese Children/Adolescents - A Preliminary Study

(J Clin Res Pediatr Endocrinol 2015; 7: 66-66)

A Preliminary Study of the Possible Role of Cannabinoid Receptor-1 (CNR1) Gene Polymorphisms in the Development of Morbid Obesity in Obese Children

(J Clin Res Pediatr Endocrinol 2015; 7: 87-87)
Baldazzi

Lilia Baldazzi

Current Loss-of-Function Mutations in the Thyrotropin Receptor Gene: When to Investigate, Clinical Effects, and Treatment

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

Hasan Balık

Thyroid Hemiagenesis: A Case Report

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

Süleyman Balkanlı

Follow-Up During Early Infancy of Newborns Diagnosed with Subcutaneous Fat Necrosis

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

Feyyaz Baltacıoğlu

Remission with Cabergoline in Adolescent Boys with Cushing’s Disease

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

Shan Bao

Association of DENND1A Gene Polymorphisms with Polycystic Ovary Syndrome: A Meta-Analysis

(J Clin Res Pediatr Endocrinol 2016; 8: 135-143)
Baradaran-Heravi

Alireza Baradaran-Heravi

Novel Mutation in the SLC19A2 Gene in an Iranian Family with Thiamine-Responsive Megaloblastic Anemia: A Series of Three Cases

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

Ahmet Baran

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

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

Ahmet Baran

Prepubertal Unilateral Gynecomastia: Report of 2 Cases

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

Bone Mineral Density in Adolescent Girls with Hypogonadotropic and Hypergonadotropic Hypogonadism

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

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)

Bone Mineral Density in Adolescent Girls with Hypogonadotropic and Hypergonadotropic Hypogonadism

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

Vatan Barışık

Screening of PROP-1, LHX2, and POU1F1 Mutations in Patients with Ectopic Posterior Pituitary Gland

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

Jesús Barreiro

Congenital Hypothyroidism with Neurological and Respiratory Alterations: A Case Detected Using a Variable Diagnostic Threshold for TSH

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

Timothy G Barrett

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

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

Naglaa Barseem

Gene Polymorphisms of Glutathione S-Transferase T1/M1 in Egyptian Children and Adolescents with Type 1 Diabetes Mellitus

(J Clin Res Pediatr Endocrinol 2017; 9: 138-143)
Basak

Dhananjoy Basak

Nifedipine in Congenital Hyperinsulinism-A Case Report

(J Clin Res Pediatr Endocrinol 2015; 7: 151-154)
Baş

Firdevs Baş

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

(J Clin Res Pediatr Endocrinol 2008; 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: -)

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: -)

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: -)

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)

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)

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)

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

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

Follow-up of Two Cases of Medulloblastoma with/without Growth Hormone Therapy

(J Clin Res Pediatr Endocrinol 2015; 7: 17-18)

Growth without Growth Hormone Syndrome in a Patient with Craniopharyngioma

(J Clin Res Pediatr Endocrinol 2015; 7: 19-19)

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

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

H Syndrome: A Rare Monogenic Cause of Insulin-Dependent Diabetes Mellitus

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

A Rare Presentation of Friedreich’s Ataxia in Pediatric Case: Diabetes Mellitus

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

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)

Premature Pubarche, Hyperinsulinemia, Hypothyroxinemia and Hyperintensities in Basal Ganglia: All Caused by a Single Congenital Defect

(J Clin Res Pediatr Endocrinol 2016; 8: 14-14)

Insulin Oedema in Newly Diagnosed Type 1 Diabetes Mellitus - Case Report

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

Hypothyroidism Due to Hepatic Hemangioendothelioma: A Case Report

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

Sporadic Nonautoimmune Neonatal Hyperthyroidism Due to A623V Germline Mutation in the Thyrotropin Receptor Gene-Case Report

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

Does Pseudohypoaldosteronism Mask the Diagnosis of Congenital Adrenal Hyperplasia?

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

Assessment of the Knowledge of Diabetes Mellitus Among School Teachers within the Scope of the Managing Diabetes at School Program

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

A Rare Combination: Congenital Adrenal Hyperplasia Due To 21 Hydroxylase Deficiency and Turner Syndrome

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

Hyperinsulinemic Hypoglycemia: Experience in A Series of 17 Cases

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

Long-Term Follow-Up of Cushing’s Disease: A Case Report

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

Evaluation of Asymmetric Dimethylarginine (ADMA) Levels in Children with Growth Hormone Deficiency

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

Prader-Willi Syndrome and Growth Hormone Deficiency

(J Clin Res Pediatr Endocrinol 2014; 6: 62-67)

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

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

Phenotype-Genotype Correlations in Bardet-Biedl Syndrome Patients with Molecular Analysis

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

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)
Başaran

Seher Başaran

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

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

Homozygous SHOX Gene Deletion Detected by Array-CGH in a Girl with Langer Mesomelic Dysplasia

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

Murat Başaranoğlu

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

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

Burak Başer

8Q22.3-Q24.23 Duplication: A Case Report

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

İbrahim Başol

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

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

Osman Baştuğ

Congenital Hypothyroidism Due To Maternal Radioactive Iodine Exposure During Pregnancy

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

Body Weight, Length and Head Circumference at Birth in a Cohort of Turkish Newborns

(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)

Dermal and Ophthalmic Findings in Pseudohypoaldosteronism

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

Maternal Obesity and its Short- and Long-Term Maternal and Infantile Effects

(J Clin Res Pediatr Endocrinol 2016; 8: 114-124)

Complex Glycerol Kinase Deficiency and Adrenocortical Insufficiency in Two Neonates

(J Clin Res Pediatr Endocrinol 2016; 8: 468-471)
Batajoo

Ruby Joshi Batajoo

Long-term Efficacy of Insulin Pump Therapy in Children with Type 1 Diabetes Mellitus

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

Louise Bath

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

Adnan Batman

Late-Onset Congenital Adrenal Hyperplasia Diagnosed at 53 Years of Age

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

Fatih Battal

The Effects of Passive Smoking on the Six-Minute Walk Test in Obese Pediatric Cases

(J Clin Res Pediatr Endocrinol 2014; 6: 245-249)
Battaloğlu İnanç

Betül Battaloğlu İnanç

Metabolic Syndrome in School Children

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

Jeannine Baumgartner

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)
Bay

Ali Bay

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

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

Petek Bayındır

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

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

Murat Baykara

Association Between Apolipoprotein E Polymorphism and Subclinic Atherosclerosis in Patients with Type 1 Diabetes Mellitus

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

İlkay Koray Bayrak

A Male Case of Aromatase Deficiency with a Novel CYP19A1 Mutation

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

Elvan Bayramoğlu

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)
Baysal

Birsen Baysal

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

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

Association Between the Corrected QT Interval and Carotid Artery Intima-Media Thickness in Obese Children - Original Article

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

Williams Syndrome Associated with Isolated Growth Hormone Deficiency: Is It Just a Coincidence?

(J Clin Res Pediatr Endocrinol 2017; 9: 18-18)
Baysan

Oben Baysan

Cardiac Autonomic Functions in Obese Children - Original Article

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

Leyla Baysan Arabacı

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)
Bebova

Pavla Bebova

Normal Bone Turnover in Transient Hyperphosphatasemia

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

Beyza Belde Doğan

A Case of 46,XX DSD Due to a Novel Mutation in P450 Oxidoreductase Gene

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

Ayşenil Belger

Effects of Diabetic Ketoacidosis on Visual and Verbal Neurocognitive Function in Young Patients Presenting with New-Onset Type 1 Diabetes

(J Clin Res Pediatr Endocrinol 2015; 7: 203-210)
Belyavskaya

Elena Belyavskaya

A Long Follow-Up of a Juvenile Case with Adrenal Cortical and Medullary Hyperplasia

(J Clin Res Pediatr Endocrinol 2015; 7: 54-54)
Berberoğlu

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: -)

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)
Berdeli

Afig Berdeli

Multiple Endocrine Neoplasia Type 4 (MEN4) Syndrome

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

Abdullah Bereket

Constitutional Growth Delay Pattern of Growth in Velo-Cardio-Facial Syndrome: Longitudinal follow up and final height of two cases - Case Report

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

Diagnosis of Growth Hormone Deficiency: the role of Growth Hormone (GH), Insulin-Like Growth Factor (IGF-I) and IGF-Binding Protein (IGFBP-3)

(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: -)

Serum Alkaline Phosphatase Levels in Healthy Children and Evaluation of Alkaline Phosphatase z-scores in Different Types of Rickets - Original Article

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

Current Status of Childhood Obesity and its Associated Morbidities in Turkey

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

A Giant Ovarian Cyst in a Neonate with Classical 21-Hydroxylase Deficiency with Very High Testosterone Levels Demonstrating a High-Dose Hook Effect

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

Follow-up of Two Cases of Medulloblastoma with/without Growth Hormone Therapy

(J Clin Res Pediatr Endocrinol 2015; 7: 17-18)

Growth without Growth Hormone Syndrome in a Patient with Craniopharyngioma

(J Clin Res Pediatr Endocrinol 2015; 7: 19-19)

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)

Normative Data of Thyroid Volume-Ultrasonographic Evaluation of 422 Subjects Aged 0-55 Years

(J Clin Res Pediatr Endocrinol 2015; 7: 98-101)

H Syndrome: A Rare Monogenic Cause of Insulin-Dependent Diabetes Mellitus

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

A Rare Presentation of Friedreich’s Ataxia in Pediatric Case: Diabetes Mellitus

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

Effect of Maternal Factors and Fetomaternal Glucose Homeostasis on Birth Weight and Postnatal Growth

(J Clin Res Pediatr Endocrinol 2015; 7: 168-174)

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)

Endocrinologic Consequences of Pediatric Posterior Fossa Tumours

(J Clin Res Pediatr Endocrinol 2015; 7: 253-259)

Premature Pubarche, Hyperinsulinemia, Hypothyroxinemia and Hyperintensities in Basal Ganglia: All Caused by a Single Congenital Defect

(J Clin Res Pediatr Endocrinol 2016; 8: 14-14)
Berk

Ömer Berk

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: -)
Bernabe-García

Mariela Bernabe-García

The 13C-Glucose Breath Test for Insulin Resistance Assessment in Adolescents: Comparison with Fasting and Post-Glucose Stimulus Surrogate Markers of Insulin Resistance

(J Clin Res Pediatr Endocrinol 2016; 8: 419-424)
Bernard

Daniel J. Bernard

Delayed Adrenarche may be an Additional Feature of Immunoglobulin Super Family Member 1 Deficiency Syndrome

(J Clin Res Pediatr Endocrinol 2016; 8: 86-91)
Bideci

Aysun Bideci

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: -)

Physiology of Growth Hormone Secretion

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

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: -)

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

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

Thyroid Abnormalities in Survivors of Childhood Cancer

(J Clin Res Pediatr Endocrinol 2014; 6: 144-151)

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

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

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 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)

Attitudes of Pediatricians Regarding Prevention and Treatment of Vitamin D Deficiency

(J Clin Res Pediatr Endocrinol 2016; 8: 368-371)

Effect of Cytokine Signaling 3 Gene Polymorphisms in Childhood Obesity

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

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

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

Thyroid Hormone Resistance P453A Mutation

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

Johanne Le Bihan

An Obese Case with Homozygous Leptin Receptor Mutation

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

Asburçe Bike Olgaç

Investigation of LDLR Gene Mutations in Turkish Patients with Familial Hypercholesterolemia

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

Hatice Bilgili

Insulin Oedema in Newly Diagnosed Type 1 Diabetes Mellitus - Case Report

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

Assessment of the Knowledge of Diabetes Mellitus Among School Teachers within the Scope of the Managing Diabetes at School Program

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

Hüseyin Bilgin

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

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

Thyroid Function in Obese Children with Non-Alcoholic Fatty Liver Disease

(J Clin Res Pediatr Endocrinol 2014; 6: 152-157)

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

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

Kaya Bilguvar

Hyperandrogenism and Skeletal Dysplasia: Evaluation of 7 Patients with PAPSS2 Gene Mutation

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

Pelin Bilir

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: -)

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: -)

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: -)

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: -)

Tuberculous Meningitis Associated with Diabetic Ketoacidosis

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

Çiğdem Binay

Premature Menarche Associated with McCune-Albright Syndrome in an Infant

(J Clin Res Pediatr Endocrinol 2015; 7: 11-11)

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)

Cellular Trace Element Changes in Type 1 Diabetes Patients

(J Clin Res Pediatr Endocrinol 2016; 8: 180-186)

Gonadoblastoma and Papillary Tubal Hyperplasia in Ovotesticular Disorder of Sexual Development

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

Serum Irisin and Oxytocin Levels as Predictors of Metabolic Parameters in Obese Children

(J Clin Res Pediatr Endocrinol 2017; 9: 124-131)
Binessa

Huda Binessa

Clinical and Genetic Features of Our Patients with Hypophosphatemic Rickets

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

Fatih Binnetoğlu

The Effects of Passive Smoking on the Six-Minute Walk Test in Obese Pediatric Cases

(J Clin Res Pediatr Endocrinol 2014; 6: 245-249)
Bircan

İffet Bircan

Genetics of Obesity

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

Wolcott-Rallison Syndrome Due to a Novel Mutation (R491X) in EIF2AK3 Gene

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

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)

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)

An Infantile Hypophosphatasia Patient with a Homozygous Mutation in the ALPS Gene

(J Clin Res Pediatr Endocrinol 2015; 7: 79-79)

Pyridoxine-Responsive Seizures in Infantile Hypophosphatasia and a Novel Homozygous Mutation in ALPL Gene

(J Clin Res Pediatr Endocrinol 2016; 8: 360-364)

Clinical and Molecular Genetic Analysis in Three Children with Wolfram Syndrome: A Novel WFS1 Mutation (c.2534T>A)

(J Clin Res Pediatr Endocrinol 2017; 9: 80-84)

Evaluation of the Response to the First Two Years of Growth Hormone Treatment in Kabuki Make-Up Syndrome

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

Dibakar Biswas

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: -)
Bişgin

Atıl Bişgin

A Novel GH1 Functional Mutation in a Family with Isolated Growth Hormone Deficiency

(J Clin Res Pediatr Endocrinol 2015; 7: 13-13)
Boelaert

Kristien Boelaert

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

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

Ahmet Bolat

Metabolic and Histopathological Effects of Fructose Intake During Pregestation, Gestation and Lactation in Rats and their Offspring

(J Clin Res Pediatr Endocrinol 2015; 7: 19-26)

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)

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

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

Semih Bolu

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)

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)
Bona

Gianni Bona

Subclinical Hypothyroidism in Children: Natural History and When to Treat

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

Antonio Bonillo-Perales

Thyroid Function and Thyroid Autoimmunity in Relation to Weight Status and Cardiovascular Risk Factors in Children and Adolescents: A Population-Based Study

(J Clin Res Pediatr Endocrinol 2016; 8: 157-162)
Bora

Hüseyin Bora

Thyroid Abnormalities in Survivors of Childhood Cancer

(J Clin Res Pediatr Endocrinol 2014; 6: 144-151)
Borck

Guntram Borck

Two Siblings with Mutation in the Leptin Receptor Gene

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

Arda Borlu

Neck Circumference to Assess Obesity in Preschool Children

(J Clin Res Pediatr Endocrinol 2017; 9: 17-23)
Bosnalı

Oktav Bosnalı

A Giant Ovarian Cyst in a Neonate with Classical 21-Hydroxylase Deficiency with Very High Testosterone Levels Demonstrating a High-Dose Hook Effect

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

Özlem Bostan Gayret

Vitamin D Deficiency in Children and Adolescents in Bağcılar, İstanbul

(J Clin Res Pediatr Endocrinol 2015; 7: 134-139)
Boyraz

Mehmet Boyraz

Cardiac Autonomic Functions in Obese Children - Original Article

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

Transient Neonatal Diabetes Mellitus in a Turkish Patient with Three Novel Homozygous Variants in the ZFP57 Gene

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

Relationship of Epicardial Adipose Tissue Thickness with Early Indicators of Atherosclerosis and Cardiac Functional Changes in Obese Adolescents with Metabolic Syndrome

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

Effects of ACE Inhibitors on Insulin Resistance and Lipid Profile in Children with Metabolic Syndrome

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

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)

Effect of Cytokine Signaling 3 Gene Polymorphisms in Childhood Obesity

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

Mustafa Boz

Abdominal Obesity May Be Caused by Increasing Cortisol Levels with Age

(J Clin Res Pediatr Endocrinol 2015; 7: 69-69)
Bozaykut

Abdülkadir Bozaykut

Effect of Maternal Factors and Fetomaternal Glucose Homeostasis on Birth Weight and Postnatal Growth

(J Clin Res Pediatr Endocrinol 2015; 7: 168-174)
Bozkurt

Ceyhun Bozkurt

Hypothyroidism Due to Hepatic Hemangioendothelioma: A Case Report

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

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

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

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)
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)
Braverman

Nancy Elise Braverman

Rhizomelic Chondrodysplasia Punctata Type 1 Caused by a Novel Mutation in the PEX7 Gene

(J Clin Res Pediatr Endocrinol 2015; 7: 69-72)
Breuer

Christopher Breuer

Pediatric Thyroid Disease: When is Surgery Necessary, and Who Should be Operating on Our Children?

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

Rosalind S. Brown

Autoimmune Thyroiditis in Childhood

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

Feride Bucak

Primary Adrenal Insufficiency Caused by a Novel Mutation in DAX1 Gene

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

Vitamin D Deficiency and Hashimoto’s Thyroiditis in Children and Adolescents: a Critical Vitamin D Level for This Association?

(J Clin Res Pediatr Endocrinol 2015; 7: 128-133)
Budak

Nurten Budak

Food Types in the Diet and the Nutrient Intake of Obese and Non-Obese Children - Original Article

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

Colleen Buggs-Saxton

Development and Validation of a Pediatric Endocrine Knowledge Assessment Questionnaire: Impact of ac Pediatric Endocrine Knowledge Assessment Questionnaire Intervention Study

(J Clin Res Pediatr Endocrinol 2016; 8: 411-418)
Buğrul

Fuat Buğrul

A Case of Hypocalciuric Hypercalcemia Accompanying Cystic Fibrosis

(J Clin Res Pediatr Endocrinol 2015; 7: 62-62)

Schmid Type of Metaphyseal Chondrodysplasia with COL10A1 Mutation

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

Kezban Bulan

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)
Bulduk

Erkut Baha Bulduk

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

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

Engin Burak Bulut

Inflammatory Myofibroblastic Tumor Presenting with Diabetes Insipidus in an Eight-Year-Old Boy: A Case Report

(J Clin Res Pediatr Endocrinol 2015; 7: 340-343)

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

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

Ruveyde Bundak

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: -)

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: -)

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

(J Clin Res Pediatr Endocrinol 2008; 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: -)

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

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

The Pediatric Endocrinology Forum: Summer Camps for Diabetic Children in the Southeastern Regions of Turkey

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

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: -)

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: -)

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)

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)

Neutrophil Gelatinase-Associated Lipocalin as an Early Sign of Diabetic Kidney Injury in Children

(J Clin Res Pediatr Endocrinol 2015; 7: 274-279)

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

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

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)

The Role of Adenovirus Serotype 36 in Childhood Obesity

(J Clin Res Pediatr Endocrinol 2017; 9: 3-3)
Buonocore

Federica Buonocore

CYP11A1 Mutations Result in Various Clinical Phenotypes

(J Clin Res Pediatr Endocrinol 2017; 9: 2-3)
Burgu

Berk Burgu

Transverse Testicular Ectopia: A Rare Presentation with Persistent Müllerian Duct Syndrome

(J Clin Res Pediatr Endocrinol 2014; 6: 180-182)

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)
Butler

Sandra Butler

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

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

Ayşegül Büte Yüksel

Features of Two Cases with 18q Deletion Syndrome

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

Derya Büyükayhan

Hypothalamo-Pituitary Insufficiency Associated with Ectrodactyly-Ectodermal Dysplasia-Clefting Syndrome - Case Report

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

Mithat Büyükçelik

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

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

Atilla Büyükgebiz

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: -)

Fetal and Neonatal Endocrine Disruptors

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

McCune-Albright Syndrome Mimicking Malignancy: an Endocrine Disease From Oncologist’s Perspective

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

Newborn Screening for Congenital Hypothyroidism

(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: -)

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)
Büyükinan

Muammer Büyükinan

A Case of Turner Syndrome with Concomitant 
Transient Hypogammaglobulinaemia of 
Infancy and Central Diabetes Insipidus

(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)

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

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

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)

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

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

Cenk Büyükünal

Testotoxicosis: Report of Two Cases, One with a Novel Mutation in LHCGR Gene

(J Clin Res Pediatr Endocrinol 2015; 7: 242-248)
Büyükyılmaz

Gönül Büyükyılmaz

Treatment of Growth Hormone Deficiency in Langerhans Cell Histiocytosis

(J Clin Res Pediatr Endocrinol 2015; 7: 21-21)
Bzdúch

Vladimír Bzdúch

Lack of Association Between Peripheral Activity of Thyroid Hormones and Elevated TSH Levels in Childhood Obesity

(J Clin Res Pediatr Endocrinol 2014; 6: 100-104)
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