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
Ebrahim-Habibi

Azadeh Ebrahim-Habibi

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

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

Çiğdem Ecevit

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

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

Tuba Edgünlü

Homozygous Ala65Pro Mutation with V89L Polymorphism in SRD5A2 Deficiency

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

Chandra Edwin

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)
Ekbote

Alka V. Ekbote

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

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

Damla Eker

Investigation of CYP21A2 Gene Variants in Patients Pre-diagnosed with Congenital Adrenal Hyperplasia

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

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

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

Osayame A. Ekhaguere

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

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

Beray Selver Eklioğlu

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)
Ekmahachai

Molrudee Ekmahachai

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

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

Amany Kamal El-Hawary

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

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

El-Ziny Magdy Abd El-Monem

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

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

Hosam Fathy El-Saadany

The Role of Osteopontin in the Pathogenesis and Complications of Type 1 Diabetes Mellitus in Children

(J Clin Res Pediatr Endocrinol 2016; 8: 399-404)
Elçioğlu

Huriye Nursel Elçioğlu

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)

Microcephalic Osteodysplastic Primordial Dwarfism Type Two

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

Maha E. Elhassan

Associations of Prenatal and Perinatal Factors with Cortisol Diurnal Pattern and Reactivity to Stress at Preschool Age Among Children Living in Poverty

(J Clin Res Pediatr Endocrinol 2015; 7: 114-120)
Ellard

Sian Ellard

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

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

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

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

Clinical and Molecular Characterisation of Patients with Congenital Hyperinsulinism

(J Clin Res Pediatr Endocrinol 2015; 7: 5-5)

Genetics and Clinical Characteristics of Neonatal Diabetes

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

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)

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

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

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

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

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

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

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

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

Clinical and Genetic Characteristics, Management and Long-Term Follow-Up of Turkish Patients with Congenital Hyperinsulinism

(J Clin Res Pediatr Endocrinol 2016; 8: 197-204)

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)

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

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

Hamit Yaşar Ellidağ

High-Dose Hook Effect in 17-Hydroxyprogesterone Assay in a Patient with 21-Hydroxylase Deficiency

(J Clin Res Pediatr Endocrinol 2015; 7: 329-332)

Basal Serum Neurokinin B Levels in Differentiating Idiopathic Central Precocious Puberty from Premature Thelarche

(J Clin Res Pediatr Endocrinol 2017; 9: 101-105)
Elmaoğulları

Selin Elmaoğulları

Prevalence of Dyslipidemia and Associated Factors in Obese Children and Adolescents

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

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

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

Angelo Elmi

Characteristics of Children with Type 1 Diabetes and Persistent Suboptimal Glycemic Control

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

Mona Elsamalehy

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)
Elsharkawy

Ashraf Abd-Elmoneim Elsharkawy

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

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

Hamdi Cihan Emeksiz

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

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

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

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

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

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

A Hypogonadotropic Hypogonadism Case as a Consequence of GNRHR Mutation

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

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)

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)

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

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

Sirhan Emiksiyev

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

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

Özlem Engiz

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: -)

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

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

Arzu Ensari

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: -)
Er

Eren Er

A Case of Type 1 Diabetes Mellitus with Klinefelter’s Syndrome

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

Metabolic Bone Disease of Prematurity: Report of Four Cases

(J Clin Res Pediatr Endocrinol 2014; 6: 111-115)
Eraslan

Cenk Eraslan

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

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

Ayten Eraydın

Major Depression and Fabry Disease: A Case Report

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

Pınar Dündar Erbay

Evaluation of Nutritional Status in Turkish Adolescents as Related to Gender and Socioeconomic Status - Original Article

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

Oya Ercan

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: -)

Primary Adrenal Insufficiency Caused by a Novel Mutation in DAX1 Gene

(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)

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)

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)

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

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

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)

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 AMHR2 Gene in Two Siblings with Persistent Müllerian Duct Syndrome

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

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

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

A. Gülhan Ercan Şençiçek

A Rare Genodermatosis: H Syndrome

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

Derya Erçal

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)

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)
Erdem

Galip Erdem

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)
Erdemir

Zehra Erdemir

A Case of Dyskeratosis Congenita Associated with Hypothyroidism and Hypogonadism

(J Clin Res Pediatr Endocrinol 2015; 7: 42-42)
Erdenen

Füsun Erdenen

Abdominal Obesity May Be Caused by Increasing Cortisol Levels with Age

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

Savaş Şenay Erdeve

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

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

Abdullah Erdil

Plasma Kisspeptin Levels in Newborn Infants with Breast Enlargement

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

Ayşegül Erdoğan

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

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

Aromatase Deficiency, a Rare Syndrome: Case Report

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

Clinical Approach to Thyroid Cancer and Nodules

(J Clin Res Pediatr Endocrinol 2015; 7: 29-29)

A Young Diabetic Case with Bloom Syndrome

(J Clin Res Pediatr Endocrinol 2015; 7: 42-42)

A Case of Dyskeratosis Congenita Associated with Hypothyroidism and Hypogonadism

(J Clin Res Pediatr Endocrinol 2015; 7: 42-42)

Melanocortin-4 Receptor Mutation and Obesity

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

Multiple Endocrine Neoplasia Type 4 (MEN4) Syndrome

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

Olfactory Sulcus Hypoplasia Images in a Case of Kallmann Syndrome

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

A Novel Mutation in Deficiency of 11 β-Hydroxylase: A Possible Association with Disease Severity

(J Clin Res Pediatr Endocrinol 2015; 7: 50-50)

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

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

Features of Nine Adult Cases of Osteogenesis Imperfecta

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

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)

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)

Two Cases of Klinefelter Syndrome

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

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)

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

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

Emel Erdoğan Bakar

Neurocognitive Functions in Children and Adolescents with Subclinical Hypothyroidism

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

Şahin Erdöl

A Case of Odontohypophosphatasia and Family Investigation

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

Endocrine Dysfunctions in Patients with Inherited Metabolic Diseases

(J Clin Res Pediatr Endocrinol 2016; 8: 330-333)
Erdönmez

Dilek Erdönmez

No Relationship Between Vitamin D Status and Insulin Resistance in a Group of High School Students

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

Seda Erem Basmaz

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

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

Erdal Eren

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

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

A Rare Cause of Precocious Puberty: Hepatoblastoma - Case Report

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

Acquired Generalized Lipodystrophy Associated with Autoimmune Hepatitis and Low Serum C4 Level - Case Report

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

Clinical Course of Hyperprolactinemia in Children and Adolescents: A Review of 21 Cases - Original Article

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

Resolution of Autoimmune Oophoritis after Thymectomy in a Myasthenia Gravis Patient

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

Testicular Adrenal Rest Tumors in Patients with Congenital Adrenal Hyperplasia

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

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

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

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

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

An Obese Case with Homozygous Leptin Receptor Mutation

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

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

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

A Case of Odontohypophosphatasia and Family Investigation

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

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)

Homozygous Ala65Pro Mutation with V89L Polymorphism in SRD5A2 Deficiency

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

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

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

Serpil Erermiş

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

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

Merve Ergin

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

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

Role of Versican and ADAMTS-1 in Polycystic Ovary Syndrome

(J Clin Res Pediatr Endocrinol 2017; 9: 24-30)
Erginöz

Ethem Erginöz

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)
Ergün

Orkan Ergün

Intraoperative Parathyroid Hormone Monitoring Corroborates the Success of Parathyroidectomy in Children

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

Bekir Ergüner

HOXC4 Gene is Possibly Responsible for Lin-Gettig Syndrome

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

Ayça Törel Ergür

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

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

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: -)

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: -)

Neurocognitive Functions in Children and Adolescents with Subclinical Hypothyroidism

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

Muferet Ergüven

Complementary and Alternative Medicine in Children with Type 1 Diabetes Mellitus

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

Tülay Erkan

Muscular Type Lipodystrophy Diagnosed with Neonatal Findings: Berardinelli-Seip Congenital Lipodystrophy Type 4 and Comparison Between the Types

(J Clin Res Pediatr Endocrinol 2017; 9: 30-31)
Erkek

Nilgün Erkek

Does Pseudohypoaldosteronism Mask the Diagnosis of Congenital Adrenal Hyperplasia?

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

Pınar Erkekoğlu

Urinary Bisphenol A Levels in Girls with Idiopathic Central Precocious Puberty

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

Bahri Ermiş

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

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

Belgin Eroğlu Kesim

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

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

Meltem Erol

Vitamin D Deficiency in Children and Adolescents in Bağcılar, İstanbul

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

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)
Ersen

Atilla Ersen

Recognizing the Psychosocial Aspects of Type 1 Diabetes in Adolescents

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

Betül Ersoy

Evaluation of Nutritional Status in Turkish Adolescents as Related to Gender and Socioeconomic Status - Original Article

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

Persistent Hyperinsulinemic Hypoglycemia Due to SUR1 (ABCC8) Mutation in Newborn Twins: An Eight-Year Follow-Up

(J Clin Res Pediatr Endocrinol 2015; 7: 14-14)

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)
Ertan

Yeşim Ertan

Intraoperative Parathyroid Hormone Monitoring Corroborates the Success of Parathyroidectomy in Children

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

Multiple Endocrine Neoplasia Type 4 (MEN4) Syndrome

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

Mustafa Ertek

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

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

Biray Ertürk

A Rare GCMB Gene Mutation in an Isolated Hypoparathyroidism Case

(J Clin Res Pediatr Endocrinol 2015; 7: 59-59)
Eryılmaz

Sema Kabataş Eryılmaz

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

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

Nilüfer Erzaim

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)
Esen

İhsan Esen

Microvascular Complications in Adolescents with Type 1 Diabetes Mellitus

(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)

Menstrual Characteristics of Pubertal Girls: A Questionnaire-Based Study in Turkey

(J Clin Res Pediatr Endocrinol 2016; 8: 192-196)
Estrada-Zúñiga

Cynthia M. Estrada-Zúñiga

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

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

Nilay Etiler

Hypovitaminosis D in Obese and Overweight Schoolchildren - Original Article

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

Özdal Etlik

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

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

Olcay Evliyaoğlu

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: -)

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: -)

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: -)

Primary Adrenal Insufficiency Caused by a Novel Mutation in DAX1 Gene

(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)

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)

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)

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

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

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

(J Clin Res Pediatr Endocrinol 2016; 8: 107-107)

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 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)

Follow-up Findings in a Turkish Girl with Pseudohypoparathyroidism Type Ia Caused by a Novel Heterozygous Mutation in the GNAS Gene

(J Clin Res Pediatr Endocrinol 2017; 9: 74-79)

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

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

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 AMHR2 Gene in Two Siblings with Persistent Müllerian Duct Syndrome

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

Bahri Evren

Monogenic Diabetes Case Presented with Symptomatic Hyperglycemia and Atypical Mutation

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

New Chromosomal ins(6;7)(Q13:P22) Anomaly in Klinefelter Syndrome Detected Coincidentally in Patient with Signs of Primary Hypogonadism

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

Incidentally Detected Monogenic Diabetes Case

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

Fatih Ezgü

Effect of Cytokine Signaling 3 Gene Polymorphisms in Childhood Obesity

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

Investigation of LDLR Gene Mutations in Turkish Patients with Familial Hypercholesterolemia

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