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
Çağan

Havva Hasret Çağan

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

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

Ahmet Okay Çağlayan

A Rare Genodermatosis: H Syndrome

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

Sedat Çağlı

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

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

Taliye Çakabay

Association Between Endocrine Diseases and Serous Otitis Media in Children

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

Erkan Çakır

Relationship Between Functional Exercise Capacity and Lung Functions in Obese Chidren

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

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: -)

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)

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: -)

A Rare Case of Neonatal Diabetes due to COQ2 Gene Mutation

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

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

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

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

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

Ali S. Çalıkoğlu

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)

Neonatal Hyperthyroidism Associated with Isolated Submandibular Sialadenitis: Is it Just a Coincidence? - Case Report

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

Mustafa Çalışkan

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

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

Sevda Çam

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

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

Emine Çamtosun

ROHHAD Syndrome: Reasons for Diagnostic Difficulties in Obesity

(J Clin Res Pediatr Endocrinol 2014; 6: 254-257)

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)

Tamoxifen Treatment for Pubertal Gynecomastia in a Patient with Partial Androgen Insensitivity Syndrome

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

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)

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)

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)

Response to Anastrozole Treatment in a Case with Peutz-Jeghers Syndrome and a Large Cell Calcifying Sertoli Cell Tumor

(J Clin Res Pediatr Endocrinol 2017; 9: 168-171)
Çamurdan

Mahmut Orhun Çamurdan

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

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

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)

Physiology of Growth Hormone Secretion

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

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

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

Thyroid Hormone Resistance P453A Mutation

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

Gönül Çatlı

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)

Adipokines in Breast Milk: An Update

(J Clin Res Pediatr Endocrinol 2014; 6: 192-201)

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)

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

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

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)

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

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

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)

A Novel Mutation in Human Androgen Receptor Gene Causing Partial Androgen Insensitivity Syndrome in a Patient Presenting with Gynecomastia at Puberty

(J Clin Res Pediatr Endocrinol 2016; 8: 232-235)

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)

Can Stoss Therapy Be Used in Children with Vitamin D Deficiency or Insufficiency without Rickets?

(J Clin Res Pediatr Endocrinol 2017; 9: 150-155)

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)

The Relationship Between Glycemic Variability and Inflammatory Markers in Obese Children with Insulin Resistance and Metabolic Syndrome

(J Clin Res Pediatr Endocrinol 2017; 9: 202-207)
Çavdar

Ümit Çavdar

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)
Çayır

Atilla Çayır

Cystinosis Presenting with Findings of Bartter Syndrome - Case Report

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

Anogenital Distance in Turkish Newborns

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

Plasma Kisspeptin Levels in Newborn Infants with Breast Enlargement

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

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)

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)
Çaylan

Nilgün Çaylan

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

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

Ferhat Çekmez

Association Between Insulin Resistance and 
Oxidative Stress Parameters in Obese Adolescents with Non-Alcoholic Fatty Liver Disease

(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)

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)
Çelebi

Dilara Çelebi

Non-Genetic Factors Altering Birth and Fertility Rates

(J Clin Res Pediatr Endocrinol 2017; 9: 10-11)
Çelebi Bitkin

Eda Çelebi Bitkin

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

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

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)
Çelik

Ahmet Çelik

Intraoperative Parathyroid Hormone Monitoring Corroborates the Success of Parathyroidectomy in Children

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

Management of Childhood Thyroid Nodules: Surgical and Endocrinological Findings in a Large Group of Cases

(J Clin Res Pediatr Endocrinol 2017; 9: 222-228)

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

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

Importance of Insulin Immunoassays in the Diagnosis of Factitious Hypoglycemia

(J Clin Res Pediatr Endocrinol 2014; 6: 258-261)

Vitamin D Deficiency in Children and Adolescents

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

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)

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

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

A Case of Thanatophoric Dysplasia Type 2: A Novel Mutation

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

Fatih Çelmeli

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

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

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

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

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)

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

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

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)

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

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

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)
Çeltik

Ülgen Çeltik

Management of Childhood Thyroid Nodules: Surgical and Endocrinological Findings in a Large Group of Cases

(J Clin Res Pediatr Endocrinol 2017; 9: 222-228)
Çetin

Dilek Çetin

Plasma Kisspeptin Levels in Girls with Premature Thelarche

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

Incidentally Detected Monogenic Diabetes Case

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

Nazan Çetingül

Management of Childhood Thyroid Nodules: Surgical and Endocrinological Findings in a Large Group of Cases

(J Clin Res Pediatr Endocrinol 2017; 9: 222-228)
Çetinkalp

Şevki Çetinkalp

Diabetes from the Clinician Perspective

(J Clin Res Pediatr Endocrinol 2015; 7: 24-24)

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)

Two Cases of Klinefelter Syndrome

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

Arda Çetinkaya

A Rare Genetic Disorder: Partial Trisomy on Chromosome 21

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

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)

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: -)

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)

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: -)

The Relationship Between Perceived Family Climate and Glycemic Control in Type 1 Diabetes Mellitus Adolescent Patients

(J Clin Res Pediatr Endocrinol 2017; 9: 253-259)

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: -)

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

(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: -)

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)
Çığ

Gülnaz Çığ

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)
Çicek

Betül Çicek

Weight for Length/Height Percentiles in Infants and Young Children in Kayseri/Turkey

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

Betül Çiçek

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: -)

Arm Anthropometry Indices in Turkish Children and Adolescents: Changes Over a Three-Year Period

(J Clin Res Pediatr Endocrinol 2014; 6: 216-226)

Comparison of Updated Weight and Height Percentiles with Previous References in 6-17-Year-Old Children in Kayseri, Turkey

(J Clin Res Pediatr Endocrinol 2017; 9: 39-47)
Çil Şen

Esra Çil Şen

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

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

Abdullah Çim

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

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

Derya Çimen

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

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

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)
Çizmecioğlu

Filiz Çizmecioğlu

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)

Hypovitaminosis D in Obese and Overweight Schoolchildren - Original Article

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

(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: -)

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: -)

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)

Genetic Analysis in Our Cases with Thyroid Dysgenesis

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

Educational Needs of Adolescents Regarding Normal Puberty and Menstrual Patterns

(J Clin Res Pediatr Endocrinol 2015; 7: 312-322)
Çoban

Asuman Çoban

Hidden Toxicity in Neonatal Intensive Care Units: Phthalate Exposure in Very Low Birth Weight Infants

(J Clin Res Pediatr Endocrinol 2016; 8: 298-304)

Impact of Insulin Resistance on Insulin-Like Growth Factor-1/Insulin Like Growth Factor-Binding Protein-3 Axis and on Early Weight Gain in Small for Gestational Age Infants

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

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

Iodine Overload and Severe Hypothyroidism in Two Neonates - Case Report

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

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: -)

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

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

Özgür Çoğulu

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

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

Endocrine Disrupters and Epigenetics

(J Clin Res Pediatr Endocrinol 2015; 7: 26-27)

A Young Diabetic Case with Bloom Syndrome

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

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)

Anthropometric Measurements and Complications of Achondroplasia Patients

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

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)
Çoker

Mahmut Çoker

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

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

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