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
Hacıhamdioğlu

Bülent Hacıhamdioğlu

Genoa Syndrome and Central Diabetes Insipidus: A Case Report

(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: -)

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

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

Efficiency of Fluid Treatments with Different Sodium Concentration in Children with Type 1 Diabetic Ketoacidosis

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

Synchronous Occurrence of Papillary Carcinoma in the Thyroid Gland and Thyroglossal Duct in an Adolescent with Congenital Hypothyroidism

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

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: -)

Two Siblings with Mutation in the Leptin Receptor Gene

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

The Effect of Recombinant Growth Hormone Treatment in Children with Idiopathic Short Stature and Low Insulin-Like Growth Factor-1 Levels

(J Clin Res Pediatr Endocrinol 2015; 7: 301-306)

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

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

Gonadotropin-Releasing Hormone Analogue Treatment in Females with Moderately Early Puberty: No Effect on Final Height

(J Clin Res Pediatr Endocrinol 2016; 8: 211-217)

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

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

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)

Two Siblings with Mutation in the Leptin Receptor Gene

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

Perviz Haciyev

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

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

Anthony C. Hackney

Interrelationships Among Changes in Leptin, Insulin, Cortisol and Growth Hormone and Weight Status in Youth - Original Article

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

Suha Hadi

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

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

Amr Hakeem

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

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

Goncagül Haklar

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: -)
Haliloğlu

Belma Haliloğlu

Complementary and Alternative Medicine in Children with Type 1 Diabetes Mellitus

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

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)

Thyroid Hemiagenesis: A Case Report

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

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)
Hamajima

Takashi Hamajima

Polyarthritis Caused by Methimazole in Two Japanese Patients with Graves’ Disease

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

Mohammad K. Hamedani

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)
Hamzaoğlu

Onur Hamzaoğlu

Hypovitaminosis D in Obese and Overweight Schoolchildren - Original Article

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

Suna Hancili

Mutant Neurogenin-3 in Permanent Neonatal Diabetes and Congenital Malabsorptive Diarrhea

(J Clin Res Pediatr Endocrinol 2015; 7: 10-10)
Hansen

Torben Hansen

Subclinical Hypothyroidism in Danish Lean and Obese Children and Adolescents

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

Ole Harder

Generation of Monocyte-Derived Insulin-Producing Cells from Non-Human Primates According to an Optimized Protocol for the Generation of PCMO-Derived Insulin-Producing Cells

(J Clin Res Pediatr Endocrinol 2014; 6: 93-99)
Hargreaves

Dougal S. Hargreaves

Revised You’re Welcome Criteria and Future Developments in Adolescent Healthcare - Review

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

Joanne S. Harrell

Interrelationships Among Changes in Leptin, Insulin, Cortisol and Growth Hormone and Weight Status in Youth - Original Article

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

Shirin Hasani-Ranjbar

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

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

Enver Hasanoğlu

Attitudes of Pediatricians Regarding Prevention and Treatment of Vitamin D Deficiency

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

Mais O. Hashem

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)
Hashemipour

Mahin Hashemipour

Different Aspects of Kidney Function in Well-Controlled Congenital Hypothyroidism

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

Yusuf Kenan Haspolat

A Case of Thyroid Hormone Resistance

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

Complete Androgen Insensitivity Syndrome; the Importance of Family Screening

(J Clin Res Pediatr Endocrinol 2015; 7: 84-84)
Hassani

Noura Al Hassani

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

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

Nihal Hatipoğlu

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

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

Therapeutic Approach to Obesity in Children and Adolescents

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

The Weight and Height Percentiles in 6-18 Year Old Children in Kayseri and Comparison with Istanbul Data - Original Article

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

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

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

Insulin Resistance in Obese Children and Adolescents: HOMA-IR Cut-Off Levels in the Prepubertal and Pubertal Periods - Original Article

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

Waist Circumference and Mid-Upper Arm Circumference in Evaluation of Obesity in Children Aged Between 6 and 17 Years-Original Article

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

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

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

Micropenis: Etiology, Diagnosis and Treatment Approaches

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

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

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

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

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

Health-Related Quality of Life and Metabolic Control in Children and Adolescents with Type 1 Diabetes Mellitus

(J Clin Res Pediatr Endocrinol 2016; 8: 67-73)

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)

Pseudotumour Cerebri Presentation in a Child Under the Gonadotropin-Releasing Hormone Agonist Treatment

(J Clin Res Pediatr Endocrinol 2016; 8: 365-367)

Complex Glycerol Kinase Deficiency and Adrenocortical Insufficiency in Two Neonates

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

Non-Classical Congenital Adrenal Hyperplasia in Childhood

(J Clin Res Pediatr Endocrinol 2017; 9: 1-7)
Hatun

Şükrü Hatun

Hypovitaminosis D in Obese and Overweight Schoolchildren - Original Article

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

Metabolic Syndrome in Childhood: defining the problem

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

Vitamin D Deficiency in Children and Adolescents with Type 1 Diabetes

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

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

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

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

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

Diabetes Program at Schools in Turkey

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

Can HbA1c and One-Hour Glucose Concentration in Standard OGTT Be Used for Evaluation of Glucose Homeostasis in Childhood?

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

Features of Two Cases with 18q Deletion Syndrome

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

Metabolic Bone Disease of Prematurity: Report of Four Cases

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

Is Hyperpigmentation on the First Day of Life Always Associated with IMAGe Syndrome?

(J Clin Res Pediatr Endocrinol 2014; 6: 266-268)

HADH Mutation is a Rare Cause of Hyperinsulinaemic Hypoglycaemia

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

National Childhood Diabetes Program Activities in Turkey

(J Clin Res Pediatr Endocrinol 2015; 7: 1-6)

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

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

Genetic Analysis in Our Cases with Thyroid Dysgenesis

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

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 De Novo GATA Binding Protein 3 Mutation in a Turkish Boy with Hypoparathyroidism, Deafness, and Renal Dysplasia Syndrome

(J Clin Res Pediatr Endocrinol 2015; 7: 344-348)

Attitudes of Pediatricians Regarding Prevention and Treatment of Vitamin D Deficiency

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

Filiz Hazan

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

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

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

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

46,XY Complete Gonadal Dysgenesis: A Case Report

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

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

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

A Case with Acrodysostosis and Hormone Resistance

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

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

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

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

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

Anupama Hegde

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

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

Zeliha Hekimsoy

Vitamin D in Sickness and Health

(J Clin Res Pediatr Endocrinol 2015; 7: 27-28)
Helvacıoğlu

Didem Helvacıoğlu

Complete Androgen Insensitivity Syndrome; the Importance of Family Screening

(J Clin Res Pediatr Endocrinol 2015; 7: 84-84)
Henderson

Celia L. Henderson

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

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

Merve Nur Hepokur

Relationship Between Functional Exercise Capacity and Lung Functions in Obese Chidren

(J Clin Res Pediatr Endocrinol 2015; 7: 217-221)
Heredia

Claudia Heredia

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

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

Anne Heron

Pseudohypoparathyroidism Type 1A-Subclinical Hypothyroidism and Rapid Weight Gain as Early Clinical Signs: A Clinical Review of 10 Cases

(J Clin Res Pediatr Endocrinol 2016; 8: 432-438)
Heydari

Shirin Heydari

Inflammatory Cytokine Profiles During Exercise in Obese, Diabetic, and Healthy Children

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

Samil Hızlı

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

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

Paul Higgins

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

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

Thep Himathongkam

A Novel Mutation in Thyroid Peroxidase Gene Causing Congenital Goitrous Hypothyroidism in a German-Thai Patient

(J Clin Res Pediatr Endocrinol 2016; 8: 241-245)
Hindmarsh

Peter Hindmarsh

Pseudohypoparathyroidism Type 1A-Subclinical Hypothyroidism and Rapid Weight Gain as Early Clinical Signs: A Clinical Review of 10 Cases

(J Clin Res Pediatr Endocrinol 2016; 8: 432-438)
Hiort

Olaf Hiort

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: -)

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

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

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)
Hochberg

Ze’ev Hochberg

Pubertal Gynecomastia Coincides with Peak Height Velocity

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

William H. Hoffman

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

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

Jens-Christian Holm

Subclinical Hypothyroidism in Danish Lean and Obese Children and Adolescents

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

John W. Honour

Diagnosis of Diseases of Steroid Hormone Production, Metabolism and Action - Review

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

Steroid Assays in Paediatric Endocrinology - Review

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

Duygu Horoz

Neck Circumference to Assess Obesity in Preschool Children

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

Jayne Houghton

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)
Hruba

Zuzana Hruba

A p.(Glu809Lys) Mutation in the WFS1 Gene Associated with Wolfram-like Syndrome: A Case Report

(J Clin Res Pediatr Endocrinol 2016; 8: 482-483)
Hu

Shuang Hu

The Relationship between Maternal Gestational Impaired Glucose Tolerance and Risk of Large-for-Gestational-Age Infant: A Meta-Analysis of 14 Studies

(J Clin Res Pediatr Endocrinol 2016; 8: 264-269)
Huang

Yonglan Huang

Clinical and Mutational Features of Three Chinese Children with Congenital Generalized Lipodystrophy

(J Clin Res Pediatr Endocrinol 2017; 9: 52-57)
Hubaveshki

Stanislav Hubaveshki

Prevalence of Cryptorchidism Among Bulgarian Boys - Original Article

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

Severine Van Hulle

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

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

Khalid Hussain

Hyperinsulinaemic Hypoglycaemia: Genetic Mechanisms, Diagnosis and Management

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

Prepubertal Unilateral Gynecomastia: Report of 2 Cases

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

The Diagnosis and Management of Hyperinsulinaemic Hypoglycaemia

(J Clin Res Pediatr Endocrinol 2015; 7: 86-97)

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)

Nifedipine in Congenital Hyperinsulinism-A Case Report

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

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)

Early Presentation of Hyperinsulinism/Hyperammonemia Syndrome in Three Serbian Patients

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

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)
Hussein

Khalid Hussein

ABCC8 Frameshift Mutation in Exon 28 (c.3512delT) is a Founder Mutation for Autosomal Recessive Hyperinsulinemic Hypoglycemia in Eastern Anatolia

(J Clin Res Pediatr Endocrinol 2015; 7: 20-20)
Hwang

Jin Soon Hwang

Luteinizing Hormone Secretion during Gonadotropin-Releasing Hormone Stimulation Tests in Obese Girls with Central Precocious Puberty

(J Clin Res Pediatr Endocrinol 2016; 8: 392-398)
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