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
Abaalkhail

Bahaa Abaalkhail

Prevalence of Vitamin D Deficiency and Calcium Homeostasis in Saudi Children

(J Clin Res Pediatr Endocrinol 2016; 8: 461-467)
Abacı

Ayhan Abacı

The Effect of Insulin Resistance and Obesity on Low-Density Lipoprotein Particle Size in Children - Original Article

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

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: -)

Neonatal Diabetes Mellitus Accompanied by Diabetic Ketoacidosis and Mimicking Neonatal Sepsis: A Case Report

(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)

A Case of Central Precocious Puberty Due to Concomitant Hypothalamic Hamartoma and Juvenile Pilocytic Astrocytoma

(J Clin Res Pediatr Endocrinol 2014; 6: 183-186)

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)

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

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

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)

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)

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)

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 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 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)

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)

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)
Abalı

Saygın Abalı

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: -)

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)

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)
Abbaszadegan

Mohammad Reza Abbaszadegan

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: -)
Abdel-Badie Salem

Nanees Abdel-Badie Salem

Epidemiology of Childhood Type 1 Diabetes Mellitus in Nile Delta, Northern Egypt - A Retrospective Study

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

Nilay Abseyi

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: -)
Abuhandan

Mahmut Abuhandan

Serum Paraoxonase/Arylesterase Activity and Oxidative Stress Status in Children with Metabolic Syndrome

(J Clin Res Pediatr Endocrinol 2014; 6: 163-168)

Evaluation of Pre-Treatment and Post-Treatment S100B, Oxidant and Antioxidant Capacity in Children with Diabetic Ketoacidosis

(J Clin Res Pediatr Endocrinol 2015; 7: 109-113)
Abur

Ümmet Abur

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

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

A Male Case of Aromatase Deficiency with a Novel CYP19A1 Mutation

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

Dania Abushanab

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)
Acar

Manolya Acar

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)

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)
Achermann

John Achermann

CYP11A1 Mutations Result in Various Clinical Phenotypes

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

Deniz Acıcan

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

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

Neonatal Thyroid-Stimulating Hormone Screening as a Monitoring Tool for Iodine Deficiency in Turkey

(J Clin Res Pediatr Endocrinol 2016; 8: 187-191)
Açıkel

Cengizhan Açıkel

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)
Adal

Erdal Adal

Melnick-Needles Syndrome Associated with Growth Hormone Deficiency: A Case Report - Case Report

(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)

Recognizing the Psychosocial Aspects of Type 1 Diabetes in Adolescents

(J Clin Res Pediatr Endocrinol 2015; 7: 57-62)

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)
Adalı

Mustafa Kemal Adalı

Association Between Endocrine Diseases and Serous Otitis Media in Children

(J Clin Res Pediatr Endocrinol 2017; 9: 48-51)
Adhikari

Amita Adhikari

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)
Adıyaman

Pelin Adıyaman

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: -)
Adibi

Atoosa Adibi

Different Aspects of Kidney Function in Well-Controlled Congenital Hypothyroidism

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

Amra Adrovic

A Case of Vitamin D-Dependent Rickets Type 1A with a Novel Mutation in the Uzbek Population

(J Clin Res Pediatr Endocrinol 2016; 8: 484-489)
Agarwal

Anil K. Agarwal

Progeroid Syndrome Patients with ZMPSTE24 Deficiency Could Benefit When Treated with Rapamycin and Dimethylsulfoxide

(J Clin Res Pediatr Endocrinol 2017; 9: 31-31)

Indices of Glucose Homeostasis in Cord Blood in Term and Preterm Newborns

(J Clin Res Pediatr Endocrinol 2016; 8: 270-275)
Agarwalla

Sunil Kumar Agarwalla

Identification of Novel ROR2 Gene Mutations in Indian Children with Robinow Syndrome

(J Clin Res Pediatr Endocrinol 2014; 6: 79-83)
Aghayev

Agharza Aghayev

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

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

Pınar Işık Agras

Neonatal Diabetes Mellitus Accompanied by Diabetic Ketoacidosis and Mimicking Neonatal Sepsis: A Case Report

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

Carlos A. Aguilar-Salinas

Lower Plasma Ghrelin Levels are Found in Women with Diabetes-Complicated Pregnancies

(J Clin Res Pediatr Endocrinol 2016; 8: 425-431)
Ağladıoğlu

Sebahat Yılmaz Ağladıoğlu

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: -)
Ahmad

Afzal Ahmad

Indices of Glucose Homeostasis in Cord Blood in Term and Preterm Newborns

(J Clin Res Pediatr Endocrinol 2016; 8: 270-275)
Ahmed

Syed Fasial Ahmed

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

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

Kazuhiro Akaba

Heparin-Induced Hyperkalemia in an Extremely-Low-Birth-Weight Infant: A Case Report

(J Clin Res Pediatr Endocrinol 2014; 6: 125-128)
Akacı

Okan Akacı

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: -)
Akalın

Figen Akalın

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: -)
Akan

Gökçe Akan

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: -)

Increased Resistin Serum Concentrations in Patients with Type 1 Diabetes Mellitus

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

Ömer Salih Akar

A Male Case of Aromatase Deficiency with a Novel CYP19A1 Mutation

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

Ersin Akarsu

Major Depression and Fabry Disease: A Case Report

(J Clin Res Pediatr Endocrinol 2017; 9: 8-9)
Akay Tayfun

Gülşen Akay Tayfun

Different Genotypes in Prader-Willi Syndrome

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

Four Cases of SCD (Jarcho-Levin Syndrome) Presenting with Short Stature

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

Eren Akbaba

The Relationship Between Gestational Diabetes Mellitus and Selenoprotein-P Plasma 1 (SEPP1) Gene Polymorphisms

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

The Relationship Between Gestational Diabetes Mellitus and Selenoprotein-P Plasma 1 (SEPP1) Gene Polymorphisms

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

Ayla Akbal

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

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

Emine Demet Akbaş

Thyroid Hormone Resistance P453A Mutation

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

Abdominal Obesity May Be Caused by Increasing Cortisol Levels with Age

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

Sinem Akbay

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

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

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

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

Ayla Akca Çağlar

Thyroid Abnormalities in Survivors of Childhood Cancer

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

Neşe Akcan

Long-term Endocrine Evaluation of Childhood Brain Tumors

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

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

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

The Role of Adenovirus Serotype 36 in Childhood Obesity

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

Sema Akcurin

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

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

Halise Akça

Vitamin D Deficiency in Children and Adolescents

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

Mustafa Akçakuş

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

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

Fetal-Neonatal Ovarian Cysts-Their Monitoring and Management: Retrospective Evaluation of 20 Cases and Review of the Literature - Original Article

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

Neonatal Episodic Hypoglycemia: A Finding of Valproic Acid Withdrawal - Case Report

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

Arzu Akçay

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

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

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: -)

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: -)

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

(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: -)

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)

Association Between Endocrine Diseases and Serous Otitis Media in Children

(J Clin Res Pediatr Endocrinol 2017; 9: 48-51)

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

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

Sema Akçurin

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

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

CTLA-4 (+49A/G) Polymorphism and Type-1 
Diabetes in Turkish Children

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

Urinary Bisphenol A Levels in Girls with Idiopathic Central Precocious Puberty

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

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

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

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)

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)
Akdemir

İlyas Akdemir

Pseudohypoparathyroidism Presenting with Ventricular Arrhythmia: A Case Report

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

Öznur Akdikmen

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

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

Sinem Akgül

An Adolescent Boy with Comorbid Anorexia Nervosa and Hashimoto Thyroiditis

(J Clin Res Pediatr Endocrinol 2016; 8: 92-95)
Akgün

Abdurrahman Akgün

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

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

The Mutation Spectrum of DHCR7 Gene and Two Novel Mutations

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

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)
Akın

Alper Akın

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

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

Therapeutic Approach to Obesity in Children and Adolescents

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

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

Melnick-Needles Syndrome Associated with Growth Hormone Deficiency: A Case Report - Case Report

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

Iodine Overload and Severe Hypothyroidism in Two Neonates - Case Report

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

Fetal-Neonatal Ovarian Cysts-Their Monitoring and Management: Retrospective Evaluation of 20 Cases and Review of the Literature - Original Article

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

Familial Glucocorticoid Deficiency Type 2: A Case Report - Case Report

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

Thyroid Hypoplasia as a Cause of Congenital Hypothyroidism in Monozygotic Twins Concordant for Rubinstein-Taybi Syndrome - Case Report

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

Does Early Treatment Prevent Deafness in Thiamine-Responsive Megaloblastic Anaemia Syndrome? - Case Report

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

Vitamin D Deficiency Rickets Mimicking Pseudohypoparathyroidism

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

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

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

Congenital Hypothyroidism Due To Maternal Radioactive Iodine Exposure During Pregnancy

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

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)

An Unusual Presentation of Parathyroid Adenoma in an Adolescent: Calcific Achilles Tendinitis

(J Clin Res Pediatr Endocrinol 2015; 7: 333-335)

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

Melnick-Needles Syndrome Associated with Growth Hormone Deficiency: A Case Report - Case Report

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

Iodine Overload and Severe Hypothyroidism in Two Neonates - Case Report

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

Fetal-Neonatal Ovarian Cysts-Their Monitoring and Management: Retrospective Evaluation of 20 Cases and Review of the Literature - Original Article

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

Neonatal Episodic Hypoglycemia: A Finding of Valproic Acid Withdrawal - Case Report

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

Familial Glucocorticoid Deficiency Type 2: A Case Report - Case Report

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

Thyroid Hypoplasia as a Cause of Congenital Hypothyroidism in Monozygotic Twins Concordant for Rubinstein-Taybi Syndrome - Case Report

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

Does Early Treatment Prevent Deafness in Thiamine-Responsive Megaloblastic Anaemia Syndrome? - Case Report

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

Fetal Adrenal Suppression Due to Maternal Corticosteroid Use: Case Report

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

Vitamin D Deficiency Rickets Mimicking Pseudohypoparathyroidism

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

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

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

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)

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)
Akıncı

Ayşehan Akıncı

Glucagon-like Peptide-1 and-2 Levels in Children with Diabetic Ketoacidosis - Original Article

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

Tuberculous Meningitis Associated with Diabetic Ketoacidosis

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

Plasma Kisspeptin Levels in Girls with Premature Thelarche

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

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

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

Clinical and Genetic Approach to Lipodystrophies

(J Clin Res Pediatr Endocrinol 2015; 7: 32-32)

Heterozygous AGPAT2 Mutation, Diabetes, and Lipodystrophy in Extremities

(J Clin Res Pediatr Endocrinol 2015; 7: 53-53)

Magnetic Resonance Imaging Characteristics of a Dunnigan-Type Familial Partial Lipodystrophy Patient

(J Clin Res Pediatr Endocrinol 2015; 7: 61-61)

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)

Progeroid Syndrome Patients with ZMPSTE24 Deficiency Could Benefit When Treated with Rapamycin and Dimethylsulfoxide

(J Clin Res Pediatr Endocrinol 2017; 9: 31-31)

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)
Akkoyun

Esra Betül Akkoyun

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

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

Gamze Akkuş

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)

Hypogonadotropic Hypogonadism due to Novel FGFR1 Mutations

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

İhsan Akpınar

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

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

Nurten Aksoy

Evaluation of Pre-Treatment and Post-Treatment S100B, Oxidant and Antioxidant Capacity in Children with Diabetic Ketoacidosis

(J Clin Res Pediatr Endocrinol 2015; 7: 109-113)
Aksu

Hatice Aksu

The Effect of Congenital and Postnatal Hypothyroidism on Depression-Like Behaviors in Juvenile Rats

(J Clin Res Pediatr Endocrinol 2016; 8: 439-444)
Aktaş Samur

Anıl Aktaş Samur

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

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

Bedir Akyol

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: -)
Akyürek

Fikret Akyürek

Heart-Type Fatty Acid Binding Protein Level as a Tool in Identification of Early Cardiac Effects of Diabetic Ketoacidosis

(J Clin Res Pediatr Endocrinol 2017; 9: 118-123)

Reevaluation of the Prevalence of Metabolic 
Syndrome in an Urban Area of Turkey

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

Ambulatory Blood Pressure and Subclinical Cardiovascular Disease in Patients with Congenital Adrenal Hyperplasia: A Preliminary Report

(J Clin Res Pediatr Endocrinol 2015; 7: 13-18)

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)

Assessment of Cardiovascular Parameters in Obese Children and Adolescents with Non-Alcoholic Fatty Liver Disease

(J Clin Res Pediatr Endocrinol 2015; 7: 222-227)

Evaluation of Periaortic Adiposity and Metabolic Disorders in Obese Children

(J Clin Res Pediatr Endocrinol 2016; 8: 74-79)

Prediabetes and Cardiovascular Parameters in Obese Children and Adolescents

(J Clin Res Pediatr Endocrinol 2016; 8: 80-85)

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)
Akyüz

Esra Akyüz

The Relationship Between Metabolic Syndrome and Left Ventricular Mass Index in Obese Children-

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

Abdulmoein Al-Agha

Metabolic Control in Children and Adolescents with Insulin-Dependent Diabetes Mellitus at King Abdul-Aziz University Hospital

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

Roua A. Al-Rijjal

Clinical and Genetic Features of Our Patients with Hypophosphatemic Rickets

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

Yasemin Alanay

A Review of the Principles of Radiological Assessment of Skeletal Dysplasias

(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: -)

Prepubertal Unilateral Gynecomastia: Report of 2 Cases

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

Genetic Approach to Osteoporosis

(J Clin Res Pediatr Endocrinol 2015; 7: 40-40)
Albanesi

Michela Albanesi

Long-term Outcome after Robotic-assisted Gastroplication in Adolescents: Hunger Hormone and Food Preference Changes Two Case Reports

(J Clin Res Pediatr Endocrinol 2016; 8: 250-256)
Aldemir

Özgür Aldemir

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

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

Ekrem Algün

Analysis of THRΒ Gene in Turkish Patients and Definition of Three Novel Pathogenic Variants

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

Ayfer Alikaşifoğlu

The Relationship Between Serum Adiponectin, Tumor Necrosis Factor-Alpha, Leptin Levels and Insulin Sensitivity in Childhood and Adolescent Obesity: Adiponectin is a Marker of Metabolic Syndrome - Original Article

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

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: -)

Need for Comprehensive Hormonal Workup in the Management of Adrenocortical Tumors in Children

(J Clin Res Pediatr Endocrinol 2014; 6: 68-73)

Growth Hormone Treatment in Childhood Intracranial Tumors - Hacettepe Experience

(J Clin Res Pediatr Endocrinol 2015; 7: 8-8)

Growth Hormone Therapy in Five Patients with Malignant Intracranial Tumors

(J Clin Res Pediatr Endocrinol 2015; 7: 9-9)

Primary Melanocytic Suprasellar Tumor Presenting with Growth Hormone Deficiency

(J Clin Res Pediatr Endocrinol 2015; 7: 15-15)

A Rare Case of Neonatal Diabetes due to COQ2 Gene Mutation

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

Treatment of Growth Hormone Deficiency in Langerhans Cell Histiocytosis

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

Ayfer Alikaşifoğlu

Editorial

(J Clin Res Pediatr Endocrinol 2015; 7: 0-0)
Alikaşifoğlu

Ayfer Alikaşifoğlu

Severe Undervirilisation in a 46,XY Case Due to a Novel Mutation in HSD17B3 Gene

(J Clin Res Pediatr Endocrinol 2015; 7: 249-252)

Hyperthyroidism After Allogeneic Hematopoietic Stem Cell Transplantation: A Report of Four Cases

(J Clin Res Pediatr Endocrinol 2015; 7: 349-354)

An Adolescent Boy with Comorbid Anorexia Nervosa and Hashimoto Thyroiditis

(J Clin Res Pediatr Endocrinol 2016; 8: 92-95)

Growth Hormone Deficiency in a Child with Neurofibromatosis-Noonan Syndrome

(J Clin Res Pediatr Endocrinol 2016; 8: 96-100)
Alioğlu

Bülent Alioğlu

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: -)
Alkuraya

Fowzan Sami Alkuraya

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)
Alonso-Fernández

Jóse Ramón Alonso-Fernández

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

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

Esma Alp

Al-Awadi/Raas-Rothschild Syndrome in a Newborn with Additional Anomalies - Case Report

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

Cystinosis Presenting with Findings of Bartter Syndrome - Case Report

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

Weismann-Netter-Stuhl Syndrome:A family report - Case Report

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

Al-Awadi/Raas-Rothschild Syndrome in a Newborn with Additional Anomalies - Case Report

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

Ambulatory Blood Pressure and Subclinical Cardiovascular Disease in Patients with Congenital Adrenal Hyperplasia: A Preliminary Report

(J Clin Res Pediatr Endocrinol 2015; 7: 13-18)

Assessment of Cardiovascular Parameters in Obese Children and Adolescents with Non-Alcoholic Fatty Liver Disease

(J Clin Res Pediatr Endocrinol 2015; 7: 222-227)

Evaluation of Periaortic Adiposity and Metabolic Disorders in Obese Children

(J Clin Res Pediatr Endocrinol 2016; 8: 74-79)

Prediabetes and Cardiovascular Parameters in Obese Children and Adolescents

(J Clin Res Pediatr Endocrinol 2016; 8: 80-85)
Alparslan

Caner Alparslan

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

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

Bilal Altan

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)

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

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

Canan Altay

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)
Altıncık

Ayça Altıncık

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: -)

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

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

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)

The Role of Thyrotropin-Releasing Hormone Stimulation Test in Management of Hyperthyrotropinemia in Infants

(J Clin Res Pediatr Endocrinol 2015; 7: 211-216)

A Novel Homozygous Mutation in the Transient Receptor Potential Melastatin 6 Gene: A Case Report

(J Clin Res Pediatr Endocrinol 2016; 8: 101-104)
Altıner

Şule Altıner

Three Male Cases with Isodicentric Y Chromosome Mosaicism Including 45,X Cell Line

(J Clin Res Pediatr Endocrinol 2015; 7: 71-71)
Altun

Demet Altun

Urinary Netrin-1: A New Biomarker for the Early Diagnosis of Renal Damage in Obese Children

(J Clin Res Pediatr Endocrinol 2016; 8: 282-287)

The Association between Serum 25-Hydroxy Vitamin D Level and Urine Cathelicidin in Children with a Urinary Tract Infection

(J Clin Res Pediatr Endocrinol 2016; 8: 325-329)

Features of Nine Adult Cases of Osteogenesis Imperfecta

(J Clin Res Pediatr Endocrinol 2015; 7: 52-52)

Two Cases of Testicular Adrenal Rest Tumor (TART)

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

Özge Altun Köroğlu

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

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

Canan Altunay

Weight and Height Percentiles For 0-84- Month-Old Children in Kayseri - A Central Anatolian City in Turkey

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

Engin Altundağ

Impact of CYP21A2 Gene Mutations on Clinical Management of Congenital Adrenal Hyperplasia

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

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

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

A Male Case of Aromatase Deficiency with a Novel CYP19A1 Mutation

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

Esma Altunoğlu

Abdominal Obesity May Be Caused by Increasing Cortisol Levels with Age

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

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)
Altuntaş

Yüksel Altuntaş

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

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

İbrahim Al Alwan

The Effect of Parental Socioeconomic Class on Children’s Body Mass Indices

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

Fatma Aman

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)
Amici

Mara De Amici

Long-term Outcome after Robotic-assisted Gastroplication in Adolescents: Hunger Hormone and Food Preference Changes Two Case Reports

(J Clin Res Pediatr Endocrinol 2016; 8: 250-256)
Amirbaigloo

Alireza Amirbaigloo

Functioning Adrenocortical Tumors in 
Children-Secretory Behavior

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

Parvin Amiri

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

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

Mahsa M. Amoli

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

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

Serge Amselem

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: -)
Andersson

Maria Andersson

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)
Andıran

Nesibe Andıran

Vitamin D Deficiency in Children and Adolescents

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

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)
Anık

Ahmet Anık

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: -)

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)

A Case of Central Precocious Puberty Due to Concomitant Hypothalamic Hamartoma and Juvenile Pilocytic Astrocytoma

(J Clin Res Pediatr Endocrinol 2014; 6: 183-186)

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)

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

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

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)

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)

The Relationship between Serum Zonulin Level and Clinical and Laboratory Parameters of Childhood Obesity

(J Clin Res Pediatr Endocrinol 2017; 9: 31-38)

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)
Antal

Zoltan Antal

Gender Differences in Cardiovascular Risks of Obese Adolescents in the Bronx - Original Article

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

Kwame Anyane-Yeboa

A Novel Mutation Causing Pseudohypoparathyroidism 1A with Congenital Hypothyroidism and Osteoma Cutis - Case Report

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

Memnune Yüksel Apak

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

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

Ferihan Aral

Wolfram Syndrome: Presentation of Two Cases with Type One and Type Two Diabetes Mellitus

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

Osteogenesis Imperfecta Presenting with Fractures in Pregnancy or Lactation Period: Report of Three Cases

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

Seda Aras

Four Cases of SCD (Jarcho-Levin Syndrome) Presenting with Short Stature

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

Aslıhan Araslı

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)
Araz

Mustafa Araz

Major Depression and Fabry Disease: A Case Report

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

Mehmet Argın

A Further Case of Hajdu-Cheney Syndrome Having a Novel Mutation in the NOTCH2 Gene

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

Sevil Arı Yuca

Growth Patterns of Children of Same Geographic Background Reared in Different Environments

(J Clin Res Pediatr Endocrinol 2014; 6: 233-237)

A Case of Hypocalciuric Hypercalcemia Accompanying Cystic Fibrosis

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

Heart-Type Fatty Acid Binding Protein Level as a Tool in Identification of Early Cardiac Effects of Diabetic Ketoacidosis

(J Clin Res Pediatr Endocrinol 2017; 9: 118-123)

Schmid Type of Metaphyseal Chondrodysplasia with COL10A1 Mutation

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

Serap Arıcı

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: -)
Arıkan

Ayşe Arıkan

The Role of Adenovirus Serotype 36 in Childhood Obesity

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

Ahmet Arman

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)
Arsan

Saadet Arsan

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

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

Derya Arslan

Heart-Type Fatty Acid Binding Protein Level as a Tool in Identification of Early Cardiac Effects of Diabetic Ketoacidosis

(J Clin Res Pediatr Endocrinol 2017; 9: 118-123)
Arslanoğlu

Ilknur Arslanoğlu

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: -)

Complementary and Alternative Medicine in Children with Type 1 Diabetes Mellitus

(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: -)

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)
Arslanoğlu

Sertaç Arslanoğlu

Neonatal Seizure as a Manifestation of Unrecognized Maternal Hyperparathyroidism

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

Ved Bhushan Arya

Hyperinsulinaemic Hypoglycaemia: Genetic Mechanisms, Diagnosis and Management

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

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)
Asar

Gülgün Asar

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: -)

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: -)
Asayesh

Hamid Asayesh

Association between Obesity and Parental Weight Status in Children and Adolescents

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

Khalid Aseri

Prevalence of Vitamin D Deficiency and Calcium Homeostasis in Saudi Children

(J Clin Res Pediatr Endocrinol 2016; 8: 461-467)
Aslan

Nagehan Aslan

The Role of Urbanization in Childhood Obesity

(J Clin Res Pediatr Endocrinol 2015; 7: 163-167)
Astratakis

Constantine Astratakis

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

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

Emre Asut

Homozygous Ala65Pro Mutation with V89L Polymorphism in SRD5A2 Deficiency

(J Clin Res Pediatr Endocrinol 2016; 8: 218-223)
Aşçı

Ali Aşçı

Urinary Bisphenol A Levels in Girls with Idiopathic Central Precocious Puberty

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

Semih Aşıkovalı

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

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

Emine Sevcan Ata

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

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

Neurocognitive Functions in Children and Adolescents with Subclinical Hypothyroidism

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

Mehmet Emre Atabek

The relationship between serum ghrelin levels and hair zinc concentrations in children - Original Article

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

Atherogenic Lipid Profile and Systolic Blood Pressure are Associated with Carotid Artery Intima-media Thickness in Children with Turner Syndrome - Original Article

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

Weismann-Netter-Stuhl Syndrome:A family report - Case Report

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

Metabolic Syndrome Features Presenting in Early Childhood in Alström Syndrome: A Case Report - Case Report

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

Al-Awadi/Raas-Rothschild Syndrome in a Newborn with Additional Anomalies - Case Report

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

Absence of Increase in Carotid Artery Intima-Media Thickness in Infants of Diabetic Mothers

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

The Relationship Between Metabolic Syndrome and Left Ventricular Mass Index in Obese Children-

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

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

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

Reevaluation of the Prevalence of Metabolic 
Syndrome in an Urban Area of Turkey

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

Ambulatory Blood Pressure and Subclinical Cardiovascular Disease in Patients with Congenital Adrenal Hyperplasia: A Preliminary Report

(J Clin Res Pediatr Endocrinol 2015; 7: 13-18)

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)

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)

Assessment of Cardiovascular Parameters in Obese Children and Adolescents with Non-Alcoholic Fatty Liver Disease

(J Clin Res Pediatr Endocrinol 2015; 7: 222-227)

Evaluation of Periaortic Adiposity and Metabolic Disorders in Obese Children

(J Clin Res Pediatr Endocrinol 2016; 8: 74-79)

Prediabetes and Cardiovascular Parameters in Obese Children and Adolescents

(J Clin Res Pediatr Endocrinol 2016; 8: 80-85)

Corticosterone Methyl Oxidase Deficiency Type 1 with Normokalemia in an Infant

(J Clin Res Pediatr Endocrinol 2016; 8: 356-359)

Gene Conversion and Congenital Adrenal Hyperplasia: Two Case Reports

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

F. Belgin Ataç

β-3AR W64R Polymorphism and 30-Minute Post-Challenge Plasma Glucose Levels in Obese Children

(J Clin Res Pediatr Endocrinol 2015; 7: 7-12)
Atalar

Fatmahan Atalar

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

(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: -)

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: -)
Atasay

Begüm Atasay

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

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

Ali Ataş

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

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

Evaluation of Pre-Treatment and Post-Treatment S100B, Oxidant and Antioxidant Capacity in Children with Diabetic Ketoacidosis

(J Clin Res Pediatr Endocrinol 2015; 7: 109-113)

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)

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)
Atay

Zeynep Atay

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: -)

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)

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)

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)

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)

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)
Atıcı

Aytuğ Atıcı

A Case of Thanatophoric Dysplasia Type 2: A Novel Mutation

(J Clin Res Pediatr Endocrinol 2015; 7: 73-76)
Atık

Tahir Atık

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

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

Tahir Atik

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

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

Genetic Analysis of Lipodystrophies and Recently Found Mutations

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

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)

RET Mutation Spectrum in Turkish Cases with Medullary Thyroid Carcinoma: Definition of a Novel K710R Mutation

(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)

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

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

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)

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)

HOXC4 Gene is Possibly Responsible for Lin-Gettig Syndrome

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

A Case of SHOX Gene Deletion Diagnosed By Microarray

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

Yasemin Atik Altınok

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

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

Dinçer Atila

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

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

Ayşegül Atmaca

A Male Case of Aromatase Deficiency with a Novel CYP19A1 Mutation

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

Salima Attia

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)
Avanoğlu

Ali Avanoğlu

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

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

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

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

Parental View on the Terminology of Disorders of Sex Development

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

Yahya Avcı

Prepubertal Unilateral Gynecomastia: Report of 2 Cases

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

Zeynep Avcıl

The Role of Adiponectin During Placental Development in Streptozotocin-Induced Rats

(J Clin Res Pediatr Endocrinol 2015; 7: 64-64)
Ay

Yılmaz Ay

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

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

Canan Ayabakan

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: -)
Ayaz

Teslime Ayaz

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)
Aycan

Zehra Aycan

Obesity in Childhood: definition and epidemiology

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

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: -)

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: -)

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

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

Eight-Year Follow-up of a Girl with McCune-Albright Syndrome - Case Report

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

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: -)

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: -)

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)

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

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

Evaluation of Iodine Deficiency in Children with Attention Deficit/Hyperactivity Disorder

(J Clin Res Pediatr Endocrinol 2016; 8: 61-66)

The Growth Characteristics of Patients with Noonan Syndrome: Results of Three Years of Growth Hormone Treatment: A Nationwide Multicenter Study

(J Clin Res Pediatr Endocrinol 2016; 8: 305-312)

A Rare Cause of Short Stature: 3M Syndrome in a Patient with Novel Mutation in OBSL1 Gene

(J Clin Res Pediatr Endocrinol 2017; 9: 91-94)
Aydemir

Gökhan Aydemir

The Association between Serum 25-Hydroxy Vitamin D Level and Urine Cathelicidin in Children with a Urinary Tract Infection

(J Clin Res Pediatr Endocrinol 2016; 8: 325-329)
Aydın

Ahmet Aydın

Recognizing the Psychosocial Aspects of Type 1 Diabetes in Adolescents

(J Clin Res Pediatr Endocrinol 2015; 7: 57-62)

Sex Hormone-Binding Globulin in Children and Adolescents

(J Clin Res Pediatr Endocrinol 2016; 8: 1-12)

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

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

A Rare Genetic Disorder: Partial Trisomy on Chromosome 21

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

Distribution of RET Mutations and Evaluation of Treatment Approaches in Hereditary Medullary Thyroid Carcinoma in Turkey

(J Clin Res Pediatr Endocrinol 2016; 8: 13-20)

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

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

Congenital Goitrous Hypothyroidism, Deafness and Iodide Organification Defect in Four Siblings: Pendred or Pseudo-Pendred Syndrome? - Case Report

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

Etiological Classification and Clinical Assessment of Children and Adolescents with Disorders of Sex Development - Original Article

(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: -)

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

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

Growth Hormone Treatment in an Adolescent with Pycnodysostosis

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

Transient Congenital Hypothyroidism in Turkey: An Analysis on Frequency and Natural Course

(J Clin Res Pediatr Endocrinol 2016; 8: 170-179)

A Case Report of Xp21 Contiguous Gene Syndrome: Adrenal Hypoplasia Congenita, Glycerol Kinase Deficiency, and Duchenne Muscular Dystrophy

(J Clin Res Pediatr Endocrinol 2016; 8: 14-15)

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

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

A Rare Cause of Obesity: ROHHAD Syndrome

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

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

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

Glucagon-like Peptide-1 and-2 Levels in Children with Diabetic Ketoacidosis - Original Article

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

Thyroid Hormone Levels in Obese Children and Adolescents with Non-Alcoholic Fatty Liver Disease

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

Neonatal Thyroid-Stimulating Hormone Screening as a Monitoring Tool for Iodine Deficiency in Turkey

(J Clin Res Pediatr Endocrinol 2016; 8: 187-191)
Aydıner

Ömer Aydıner

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

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

Seçil Aydınöz

Ghrelin Levels and Postnatal Growth in Healthy Infants 0-3 Months of Age - Original Article

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

Ayşe Aygün

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: -)
Aykut

Ayça Aykut

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)

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

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

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

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

RET Mutation Spectrum in Turkish Cases with Medullary Thyroid Carcinoma: Definition of a Novel K710R Mutation

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

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)

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

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

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)
Aylanç

Hakan Aylanç

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

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

Ebru Aypar

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: -)
Aysoy

Cevriye Aysoy

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: -)
Aytaç Kaplan

Emel Hatun Aytaç Kaplan

Case Report of Leri-Weill Dyscontrosteosis Caused By SHOX Gene Deletion

(J Clin Res Pediatr Endocrinol 2017; 9: 14-14)
Azizi

Fereidoun Azizi

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

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