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
Cabanas

Paloma Cabanas

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

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

Zeynep Caferoğlu

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)
Cai

Jun-Hong Cai

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

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

Valeria Calcaterra

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)
Callewaert

Bert Callewaert

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

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

Demet Can

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)

A Case of Thyroid Hormone Resistance

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

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)

A Novel Pathogenic DNA Variation in the OCRL1 Gene in Lowe Syndrome - Case Report

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

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

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

Diabetic Ketoacidosis Presenting with Pseudonormoglycemia in a 15-Year-Old Girl 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)

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)

A Family with Multiple Endocrine Neoplasia Type 2A: Importance of Early Prophylactic Thyroidectomy

(J Clin Res Pediatr Endocrinol 2015; 7: 92-92)
Can Yılmaz

Gülay Can Yılmaz

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

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

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)

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)

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

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

A Rare Cause of Obesity: ROHHAD Syndrome

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

Özden Canbay

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)
Cangül

Hakan Cangül

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

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

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 Homozygous Nonsense Thyroid Peroxidase Mutation (R540X) Consistently Causes Congenital Hypothyroidism in Two Siblings Born to a Consanguineous Family

(J Clin Res Pediatr Endocrinol 2015; 7: 323-328)
Carel

Jean Claude Carel

Hyperthyroidism in Childhood: Causes, When and How to Treat

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

Ian M. Carr

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)
Cassio

Alessandra Cassio

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

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

Luis Antonio Castaño

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

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

Lidia Castro-Feijoo

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

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

Ayşe Nurcan Cebeci

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: -)

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: -)

Higher Body Fat and Lower Fat-Free Mass in Girls with Premature Adrenarche

(J Clin Res Pediatr Endocrinol 2015; 7: 45-48)

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)
Celayir

Ayşenur Celayir

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: -)
Celen Kaya

Esra Celen Kaya

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)
Cena

Hellas Cena

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)
Cengiz

Pınar Cengiz

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: -)
Cerrah Güneş

Meltem Cerrah Güneş

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

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

FGFR2 Gene Mutations in Patients with Syndromic or Isolated Craniosynostosis

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

Ol’ga Cervenová

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

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

Barbora Cervickova

Normal Bone Turnover in Transient Hyperphosphatasemia

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

Gökhan Cesur

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

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

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: -)

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: -)

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

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

Distribution of Gene Mutations Associated with Familial Normosmic Idiopathic Hypogonadotropic Hypogonadism

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

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

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

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

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

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)

Correlation of Brain Neuropeptide (Nesfatin-1 and Orexin-A) Concentrations with Anthropometric and Biochemical Parameters in Malnourished Children

(J Clin Res Pediatr Endocrinol 2015; 7: 197-202)

Relationship Between Functional Exercise Capacity and Lung Functions in Obese Chidren

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

Emine İpek Ceylan

FGFR2 Gene Mutations in Patients with Syndromic or Isolated Craniosynostosis

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

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

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

Serdar Ceylaner

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

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

Primary Adrenal Insufficiency Caused by a Novel Mutation in DAX1 Gene

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

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)

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

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

Coexistence of Kabuki Syndrome and Autoimmune Thyroiditis

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

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)

Crouzonodermoskeletal Syndrome with Hypoplasia of Corpus Callosum and Inferior Vermis

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

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)

Delayed Diagnosis of a 17-Hydroxylase/17,20-Lyase Deficient Patient Presenting as a 46,XY Female: A Low Normal Potassium Level Can Be an Alerting Diagnostic Sign

(J Clin Res Pediatr Endocrinol 2017; 9: 163-167)

A Novel Mutation in INSR Gene in a Child Presenting with Acanthosis Nigricans

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

An Infant with Leydig Cell Hypoplasia Presenting with Bilateral Inguinal Masses

(J Clin Res Pediatr Endocrinol 2017; 9: 5-5)
Chai

Jian Chai

Screening of HHEX Mutations in Chinese Children with Thyroid Dysgenesis

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

Parsa Y. Chaijan

Epidemiology of Congenital Hypothyroidism in Markazi Province, Iran

(J Clin Res Pediatr Endocrinol 2014; 6: 105-110)
Chalaby Mohamed

Nehad Chalaby Mohamed

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

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

Angel O. K. Chan

Corticosterone Methyl Oxidase Deficiency Type 1 with Normokalemia in an Infant

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

Abalo Chango

Environmental Contaminants and Pancreatic Beta-Cells

(J Clin Res Pediatr Endocrinol 2016; 8: 257-263)
Chanprasertyothin

Suwannee Chanprasertyothin

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)
Chatterjee

Daipayan Chatterjee

Safety and Efficacy of Stosstherapy in Nutritional Rickets

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

Safety and Efficacy of Stosstherapy in Nutritional Rickets

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

Nifedipine in Congenital Hyperinsulinism-A Case Report

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

Nitin Chaubal

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

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

Ronak S. Chaudhari

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

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

Vasundhara Sridhar Chennuri

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

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

Przemyslawa Jarosz- Chobot

L-thyroxine Stabilizes Autoimmune Inflammatory Process in Euthyroid Nongoitrous Children with Hashimoto’s Thyroiditis and Type 1 Diabetes Mellitus

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

Subhankar Chowdhury

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: -)
Cianfarani

Stefano Cianfarani

Controversies in the Definition and Treatment of Idiopathic Short Stature (ISS) - Review

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

Murat Cihan

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

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

Emine Ayça Cimbek

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

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

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)
Cinaz

Peyami Cinaz

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)

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)

Effect of Cytokine Signaling 3 Gene Polymorphisms in Childhood Obesity

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

Thyroid Hormone Resistance P453A Mutation

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

Matthew G Clark

Variability of DKA Management Among Pediatric Emergency Room and Critical Care Providers: A Call for More Evidence-Based and Cost-Effective Care?

(J Clin Res Pediatr Endocrinol 2014; 6: 190-191)
Clément

Karine Clément

An Obese Case with Homozygous Leptin Receptor Mutation

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

Fran R. Cogen

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

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

Kevin Colclough

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)
Colón

Cristóbal Colón

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

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

Jennifer Cook

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)
Cooper

Charlton Cooper

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)
Corrias

Andrea Corrias

Thyroid Nodules in Pediatrics: Which Ones Can Be Left Alone, Which Ones Must be Investigated, When and How

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

Thyroid Involvement in Two Patients with Bannayan-Riley-Ruvalcaba Syndrome

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

Salih Coşkun

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

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

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: -)
Couce

M.Luz Couce

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

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

Margarita Craen

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

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