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
Galassetti

Pietro R. Galassetti

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

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

Rafael Galera-Martínez

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

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

Thilini Gamage

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

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

Icíar García-Escobar

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

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

Eduardo García-Fuentes

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

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

Emilio García-García

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

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

MK Garg

A Study of Insulin Resistance by HOMA-IR and its Cut-off Value to Identify Metabolic Syndrome in Urban Indian Adolescents

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

Muazzez Garipağaoğlu

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

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

Maria Garzon

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

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

Yinlin Ge

Screening of HHEX Mutations in Chinese Children with Thyroid Dysgenesis

(J Clin Res Pediatr Endocrinol 2016; 8: 21-25)
Gebremariam

Achamyeleh Gebremariam

Relationship Between Timing of Peak Height Velocity and Pubertal Staging in Boys and Girls

(J Clin Res Pediatr Endocrinol 2015; 7: 235-237)
Gedik

Yusuf Gedik

Cleidocranial Dysplasia: A Case Report

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

Asuman Gedikbaşı

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

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

Mitchell E. Geffner

Growth Hormone Replacement Therapy: Transition from Adolescence to Adulthood - Review

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

Aromatase Inhibitors to Augment Height: Continued Caution and Study Required - Review

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

The Genetics of Growth and Growth Disorders: From the Hypothalamus to the Epiphysis

(J Clin Res Pediatr Endocrinol 2016; 8: 7-8)

Efficacy and Safety of Long-Acting Gonadotropin Releasing Hormone Analogs

(J Clin Res Pediatr Endocrinol 2016; 8: 10-10)

Congenital Adrenal Hyperplasia: Consensus Guidelines and Beyond

(J Clin Res Pediatr Endocrinol 2016; 8: 12-13)
Genç

Abdülkadir Genç

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)

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

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

Mikayir Genenş

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)
Geyikli

İclal Geyikli

Increased Resistin Serum Concentrations in Patients with Type 1 Diabetes Mellitus

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

Nosrat Ghaemi

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: -)
Ghahraman

Martha Ghahraman

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: -)
Ghazi Ali

Asghar Mirsaeid Ghazi Ali

Functioning Adrenocortical Tumors in 
Children-Secretory Behavior

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

Alaleh Gheissari

Different Aspects of Kidney Function in Well-Controlled Congenital Hypothyroidism

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

Sujoy Ghosh

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

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

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

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

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

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

Medical Management of Thyroid Ectopia: Report of Three Cases

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

Primary Hyperparathyroidism Masquerading as Rickets: Diagnostic Challenge and Treatment Outcomes

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

Nurten Girgin

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: -)
Giri

Dinesh Giri

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

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

Mushtaq Ahmed Godil

Effect of Pioglitazone on the Course of New-Onset Type 1 Diabetes Mellitus

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

Evangelia Gole

Identification and Functional Characterization of a Calcium-Sensing Receptor Mutation in an Infant with Familial Hypocalciuric Hypercalcemia

(J Clin Res Pediatr Endocrinol 2016; 8: 341-346)
Gómez-Díaz

Rita Angélica Gómez-Díaz

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

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

Carmen Gómez-Lado

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

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

Monica P. Gómez-Medina

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

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

Erwin A. Gorter

Vitamin D Deficiency in Pediatric Fracture Patients: Prevalence, Risk Factors, and Vitamin D Supplementation

(J Clin Res Pediatr Endocrinol 2016; 8: 445-451)
Göçmen

İsmail Göçmen

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

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

Faysal Gök

Elevated Urinary T Helper 1 Chemokine Levels in Newly Diagnosed Hypertensive Obese Children

(J Clin Res Pediatr Endocrinol 2015; 7: 175-182)
Gökalp

Emir Gökalp

Dermal and Ophthalmic Findings in Pseudohypoaldosteronism

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

İbrahim Gökce

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: -)
Gökçay

Gülbin Gökçay

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

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

Mehmet İlker Gökçe

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

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

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

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

Cem Gökçen

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

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

Sonay Gökoğlu

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

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

Damla Gökşen

Serum Adiponectin and hsCRP Levels and Non-Invasive Radiological Methods in the Early Diagnosis of Cardiovascular System Complications in Children and Adolescents with Type 1 Diabetes Mellitus

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

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

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

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

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

The Impact of Psycho-Educational Training on the Psychosocial Adjustment of Caregivers of Osteogenesis Imperfecta Patients

(J Clin Res Pediatr Endocrinol 2014; 6: 84-92)

Intraoperative Parathyroid Hormone Monitoring Corroborates the Success of Parathyroidectomy in Children

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

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

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

Approach to Monogenic Diabetes

(J Clin Res Pediatr Endocrinol 2015; 7: 25-25)

Melanocortin-4 Receptor Mutation and Obesity

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

The Case of Transient Neonatal Diabetes Mellitus Associated with 6q24

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

Features of Nine Adult Cases of Osteogenesis Imperfecta

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

Chromosomal Abnormalities in 344 Patients who Were Referred to Cytogenetics Laboratory with Pre-Diagnosis of Short Stature, Turner Syndrome and Sex Developmental Disorders

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

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

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

Growth curves for Turkish Girls with Turner Syndrome: Results of the Turkish Turner Syndrome Study Group

(J Clin Res Pediatr Endocrinol 2015; 7: 183-191)

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

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

Damla Gökşen Şimşek

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: -)

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

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

Renal Anomalies Associated with Ectopic Neurohypophysis - Original Article

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

Clinical Course of Hashimoto's Thyroiditis and Effects of Levothyroxine Therapy on the Clinical Course of the Disease in Children and Adolescents

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

Emine Göktaş

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

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

E. Nazlı Gönç

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)

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: -)

Editorial

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

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)

Growth Hormone Deficiency in a Child with Neurofibromatosis-Noonan Syndrome

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

Deniz Gönülal

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)
Görmüş

Uzay Görmüş

Hypovitaminosis D in Obese and Overweight Schoolchildren - Original Article

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

Orhan Görükmez

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

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

Andrea Granados

Relationship Between Timing of Peak Height Velocity and Pubertal Staging in Boys and Girls

(J Clin Res Pediatr Endocrinol 2015; 7: 235-237)
Grimley

Mary Beth Grimley

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)
Guo

Man-Li Guo

A Novel c.554+5C>T Mutation in the DUOXA2 Gene Combined with p.R885Q Mutation in the DUOX2 Gene Causing Congenital Hypothyroidism

(J Clin Res Pediatr Endocrinol 2016; 8: 224-227)
Gupta

Nidhi Gupta

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)

Safety and Efficacy of Stosstherapy in Nutritional Rickets

(J Clin Res Pediatr Endocrinol 2017; 9: 63-69)
Gurbanov

Ziya Gurbanov

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

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

Carolina Gutiérrez-Repiso

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

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

Rıdvan Güçlü

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: -)
Güemes

Maria Güemes

The Diagnosis and Management of Hyperinsulinaemic Hypoglycaemia

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

Davut Gül

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)

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

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

Dermal and Ophthalmic Findings in Pseudohypoaldosteronism

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

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

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

Selvi Gülaşı

A Case of Thanatophoric Dysplasia Type 2: A Novel Mutation

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

Hande Gülcan

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)
Güldiken

Sibel Güldiken

Investigation of BRAF Hotspot Mutations in Papillary Thyroid Tumor Samples

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

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)
Güleryüz

Handan Güleryüz

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)

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)
Güleş

Alper Güleş

Relationship Between Functional Exercise Capacity and Lung Functions in Obese Chidren

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

Pamir Gülez

Factors Influencing Serum Vitamin D Concentration in Turkish Children Residing in İzmir: A Single-Center Experience

(J Clin Res Pediatr Endocrinol 2015; 7: 294-300)
Gülgün

Mustafa Gülgün

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)
Gültepe

Mustafa Gültepe

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

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

Halit Reşit Gümele

Cleidocranial Dysplasia: A Case Report

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

Hakan Gümüş

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

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

Başak Gümüş Güler

Role of Versican and ADAMTS-1 in Polycystic Ovary Syndrome

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

Murat Günay

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

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

Yasemin Gündüz

Effects of Thyroid Autoimmunity on Early Atherosclerosis in Euthyroid Girls with Hashimoto’s Thyroiditis

(J Clin Res Pediatr Endocrinol 2016; 8: 150-156)
Güneş

Tamer Güneş

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: -)

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: -)

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)
Güngör

Olcay Güngör

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

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

Figen Günindi

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

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

Hülya Günöz

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

Ömer Güran

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

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

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

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

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: -)

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: -)

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

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

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

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

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

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

Growth without Growth Hormone Syndrome in a Patient with Craniopharyngioma

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

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

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

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)
Gürbüz

Fatih Gürbüz

Distribution of Gene Mutations Associated with Familial Normosmic Idiopathic Hypogonadotropic Hypogonadism

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

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

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

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

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

Coexistence of Kabuki Syndrome and Autoimmune Thyroiditis

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

Crouzon Syndrome with Hypoplasia of Corpus Callosum and Inferior Vermis

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

Wolcott-Rallison Syndrome

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

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)

Coexistence of Kabuki Syndrome and Autoimmune Thyroiditis

(J Clin Res Pediatr Endocrinol 2016; 8: 105-106)

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)

Crouzonodermoskeletal Syndrome with Hypoplasia of Corpus Callosum and Inferior Vermis

(J Clin Res Pediatr Endocrinol 2016; 8: 373-374)

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)

Wolcott-Rallison Syndrome with Novel EIF2AK3 Gene Mutation

(J Clin Res Pediatr Endocrinol 2016; 8: 496-497)

Hypogonadotropic Hypogonadism due to Novel FGFR1 Mutations

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

Börte Gürbüz Özgür

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

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

Hakan Gürkan

Application of Next-Generation Sequencing Technology for CFTR Mutation Screening

(J Clin Res Pediatr Endocrinol 2015; 7: 55-55)

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

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

Investigation of BRAF Hotspot Mutations in Papillary Thyroid Tumor Samples

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

Ceren Gürsal

Abdominal Obesity May Be Caused by Increasing Cortisol Levels with Age

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

Özlem Gürsoy Çalan

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

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

Ahmet Güven

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)

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

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

3M Syndrome: A Report of Four Cases in Two Families

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

Delirium in Diabetic Ketoacidosis: A Case Report

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

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

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

Distribution of Gene Mutations Associated with Familial Normosmic Idiopathic Hypogonadotropic Hypogonadism

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

Profile of Hypothyroidism in Down’s Syndrome

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

Remission with Cabergoline in Adolescent Boys with Cushing’s Disease

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

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

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

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)

Seven Cases of Williams-Beuren Syndrome: Endocrine Evaluation and Long-Term Follow-Up

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

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

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

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 Diabetic Infant with Homozygous LRBA Mutation: The Youngest Patient Reported

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

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)

Testicular Adrenal Rest Tumor in Two Brothers with a Novel Mutation in the 3-Beta-Hydroxysteroid Dehydrogenase-2 Gene

(J Clin Res Pediatr Endocrinol 2017; 9: 85-90)
Güzel

Savaş Güzel

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

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

Banu Güzel Nur

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

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

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

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