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
Tabur

Suzan Tabur

Major Depression and Fabry Disease: A Case Report

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

Hidenori Tada

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

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

Kimberly S. Tafuri

Growth Hormone Deficiency and Diabetes Insipidus as a Complication of Endoscopic Third Ventriculostomy

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

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

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

Feride Tahmiscioğlu Bucak

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)
Tajima

Toshihiro Tajima

Early Onset of Liver Steatosis in a Japanese Girl with Maturity-Onset Diabetes of the Young Type 3 (MODY3)

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

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

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

Mohamed A. Talat

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)
Tamhankar

Parag M Tamhankar

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

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

Identification of Novel Mutations in STAR Gene in Patients with Lipoid Congenital Adrenal Hyperplasia: A First Report from India

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

Waleed Al Tamimi

Prevalence of Vitamin D Deficiency and Calcium Homeostasis in Saudi Children

(J Clin Res Pediatr Endocrinol 2016; 8: 461-467)
Tanakol

Refik Tanakol

Clinical Findings of Osteoporosis

(J Clin Res Pediatr Endocrinol 2015; 7: 37-39)

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

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

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

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

Nikhil Tandon

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: -)
Taner

Yasemen Taner

Neurocognitive Functions in Children and Adolescents with Subclinical Hypothyroidism

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

İlhan Asya Tanju

Metabolic Syndrome Features Presenting in Early Childhood in Alström Syndrome: A Case Report - Case Report

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

Seher Tanrıkulu

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

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

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

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

Sibel Tanrıverdi

Capillary Bedside Blood Glucose Measurement in Neonates: Missing a Diagnosis of Galactosemia

(J Clin Res Pediatr Endocrinol 2015; 7: 83-85)

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)
Tansuğ

Nermin Tansuğ

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)
Tarhan

Tuğba Tarhan

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: -)
Tarım

Ömer Tarım

Prevalence and Correlates of Obesity in Schoolchildren from the City of Bursa,Turkey - Original Article

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

Growth Hormone Action: growth hormone receptor, growth and metabolic effects

(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: -)

Thyroid Hormones and Growth in Health and Disease - Review

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

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

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

Testicular Adrenal Rest Tumors in Patients with Congenital Adrenal Hyperplasia

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

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)

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)

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

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

Resolution of Autoimmune Oophoritis after Thymectomy in a Myasthenia Gravis Patient

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

Ayşegül Taş

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

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

Mehmet Emre Taşçılar

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

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

Cardiac Autonomic Functions in Obese Children - Original Article

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

Mehmet Taşdan

Isolated Hypoaldosteronism: A Case Report

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

Haydar Ali Taşdemir

A Rare Cause of Obesity: ROHHAD Syndrome

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

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

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

Gene Conversion and Congenital Adrenal Hyperplasia: Two Case Reports

(J Clin Res Pediatr Endocrinol 2017; 9: 4-4)
Taşkesen

Derya Taşkesen

Serum Visfatin Levels, Adiposity and Glucose Metabolism in Obese Adolescents

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

Abdullah Taşkın

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

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

Transient Neonatal Diabetes Mellitus in a Turkish Patient with Three Novel Homozygous Variants in the ZFP57 Gene

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

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

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

Mehmet Taştan

A Case of Congenital Generalized Lipodystrophy Type 2 with Novel BSCL2 Gene Mutation

(J Clin Res Pediatr Endocrinol 2017; 9: 4-4)
Taştekin

Ebru Taştekin

Investigation of BRAF Hotspot Mutations in Papillary Thyroid Tumor Samples

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

Vedide Tavlı

Cardiac Function in Newborns with Congenital Hypothyroidism: Association with Thyroid-Stimulating Hormone Levels

(J Clin Res Pediatr Endocrinol 2015; 7: 307-311)
Tayfun

Meltem Tayfun

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)
Taylor

Norman Taylor

Corticosterone Methyl Oxidase Deficiency Type 1 with Normokalemia in an Infant

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

Fahimeh Ramezani Tehrani

Menarcheal Age and Risk of Type 2 Diabetes: A Community-Based Cohort Study

(J Clin Res Pediatr Endocrinol 2017; 9: 156-162)
Tekerek

Hüseyin Tekerek

Effect Of Hypo-and Euthyroid Status On Serum Cystatin C Levels-Original Article

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

Ali Tekin

Parental View on the Terminology of Disorders of Sex Development

(J Clin Res Pediatr Endocrinol 2017; 9: 1-2)

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)

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)

The Effects of Passive Smoking on the Six-Minute Walk Test in Obese Pediatric Cases

(J Clin Res Pediatr Endocrinol 2014; 6: 245-249)

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

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

M. Ağah Tekindal

Congenital Hypothyroidism and Bone Remodeling Cycle

(J Clin Res Pediatr Endocrinol 2017; 9: 106-110)
Telli

Onur Telli

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

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

Derya Tepe

Microvascular Complications in Adolescents with Type 1 Diabetes Mellitus

(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)

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)

Prevalence of Dyslipidemia and Associated Factors in Obese Children and Adolescents

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

Demet Terek

Neonatal Seizure as a Manifestation of Unrecognized Maternal Hyperparathyroidism

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

Şule Terzioğlu

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)

Alpha-Melanocyte-Stimulating Hormone and Agouti-Related Protein: Do They Play a Role in Appetite Regulation in Childhood Obesity?

(J Clin Res Pediatr Endocrinol 2016; 8: 40-47)
Tetiker

Tamer Tetiker

Hypogonadotropic Hypogonadism due to Novel FGFR1 Mutations

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

Başak Tezel

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

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

Yotsapon Thewjitcharoen

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)
Thiele

Susanne Thiele

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)
Tıraş

Serap Teber Tıraş

Genoa Syndrome and Central Diabetes Insipidus: A Case Report

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

L’ubica Tichá

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)
Timirci

Özlem Timirci

The Distribution of Exon 3-Deleted/Full-Length Growth Hormone Receptor Polymorphism in the Turkish Population

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

Tzer Hwu Ting

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

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

Gülay Tireli

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: -)
Tiryaki

Sibel Tiryaki

Parental View on the Terminology of Disorders of Sex Development

(J Clin Res Pediatr Endocrinol 2017; 9: 1-2)
Todorovic

Sladjana Todorovic

Early Presentation of Hyperinsulinism/Hyperammonemia Syndrome in Three Serbian Patients

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

Baran Tokar

Gonadoblastoma and Papillary Tubal Hyperplasia in Ovotesticular Disorder of Sexual Development

(J Clin Res Pediatr Endocrinol 2016; 8: 351-355)
Tokmak

Aytekin Tokmak

Role of Versican and ADAMTS-1 in Polycystic Ovary Syndrome

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

Güven Toksoy

Application of Next-Generation Sequencing Technology for CFTR Mutation Screening

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

Central Precocious Puberty in a Patient with Multiple Pituitary Hormone Deficiency Due to POU1F1 (PIT1) Gene Mutation

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

Multiple Pituitary Hormone Deficiency Associated with Pituitary Hyperplasia: A Case Report

(J Clin Res Pediatr Endocrinol 2015; 7: 81-81)

Four 46,XY DSD Cases with Novel Mutations in AR and SRD5A2 Genes

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

Analia Tomova

Prevalence of Cryptorchidism Among Bulgarian Boys - Original Article

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

Turgut Topal

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)
Topaloğlu

A. Kemal Topaloğlu

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)

Hypogonadotropic Hypogonadism due to Novel FGFR1 Mutations

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

Genetics of Growth Hormone Deficiency

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

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)

Clinical and Genetics Approaches to Hypogonadotropic Hypogonadism

(J Clin Res Pediatr Endocrinol 2015; 7: 35-35)

A Hypogonadotropic Hypogonadism Case as a Consequence of GNRHR Mutation

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

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)

Crouzonodermoskeletal Syndrome with Hypoplasia of Corpus Callosum and Inferior Vermis

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

Wolcott-Rallison Syndrome with Novel EIF2AK3 Gene Mutation

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

Isolated Hypoaldosteronism: A Case Report

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

A Case of Congenital Generalized Lipodystrophy Type 2 with Novel BSCL2 Gene Mutation

(J Clin Res Pediatr Endocrinol 2017; 9: 4-4)

The Effects of Passive Smoking on the Six-Minute Walk Test in Obese Pediatric Cases

(J Clin Res Pediatr Endocrinol 2014; 6: 245-249)

Hepatic Glycogenosis in a Patient with Type 1 Diabetes: Mauriac Syndrome vs. Congenital Glycogen Storage Disease

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

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)
Topcu

Burcu Topcu

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: -)
Topçu

Meral Topçu

Hypophosphatasia Presenting with Pyridoxine-Responsive Seizures, Hypercalcemia, and Pseudotumor Cerebri: Case Report

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

Sevilay Topçuoğlu

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: -)
Torun

Emel Torun

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

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

Relationship Between Functional Exercise Capacity and Lung Functions in Obese Chidren

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

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)
Tozkır

Hilmi Tozkır

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)
Törel Ergür

Ayça Törel Ergür

Diagnostic Algoritm in Two Different Cases with Subclinical Endocrinologic Problems

(J Clin Res Pediatr Endocrinol 2017; 9: 15-15)

A New Mutation in an Infant with Hypercalcemia

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

Birgin Törer

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)
Trachoo

Objoon Trachoo

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)
Treviño-Garza

Consuelo Treviño-Garza

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)
Tripon

Cedric Tripon

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)
Tsai

Sarah L. Tsai

Morning Cortisol Levels Affected by Sex and Pubertal Status in Children and Young Adults

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

Kiriaki Tsiroukidou

High-Sensitivity C-Reactive Protein Levels and 
Metabolic Disorders in Obese and Overweight 
Children and Adolescents

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

Charles Tuggle

Pediatric Thyroid Disease: When is Surgery Necessary, and Who Should be Operating on Our Children?

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

Hale Tuhan

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

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

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

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

Sibel Tulgar Kınık

β-3AR W64R Polymorphism and 30-Minute Post-Challenge Plasma Glucose Levels in Obese Children

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

Two Siblings with Congenital Hyperinsulinism - Homozygote and Heterozygote Mutation

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

Wolfram (DIDMOAD) Syndrome - Report of Two Siblings

(J Clin Res Pediatr Endocrinol 2015; 7: 66-66)

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

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

Congenital Hypothyroidism and Bone Remodeling Cycle

(J Clin Res Pediatr Endocrinol 2017; 9: 106-110)
Tuli

Gerdi Tuli

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

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

Özgül Tunç

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: -)

46,XY Complete Gonadal Dysgenesis: A Case Report

(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)

Genetic Diagnosis Using Whole Exome Analysis in Two Cases with Malignant Infantile Osteopetrosis

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

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

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

Genetic Diagnosis Using Whole Exome Analysis in Two Cases with Malignant Osteopetrosis of Infancy

(J Clin Res Pediatr Endocrinol 2015; 7: 356-357)

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

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

Belma Özlem Tural Balsak

MEN 2A Family

(J Clin Res Pediatr Endocrinol 2017; 9: 22-23)
Turan

Caner Turan

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)

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)

A Novel Mutation in AMHR2 Gene in Two Siblings with Persistent Müllerian Duct Syndrome

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

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)

Hypogonadotropic Hypogonadism due to Novel FGFR1 Mutations

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

Isolated Hypoaldosteronism: A Case Report

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

A Case of Congenital Generalized Lipodystrophy Type 2 with Novel BSCL2 Gene Mutation

(J Clin Res Pediatr Endocrinol 2017; 9: 4-4)

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: -)

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: -)

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: -)

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)

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)

Normative Data of Thyroid Volume-Ultrasonographic Evaluation of 422 Subjects Aged 0-55 Years

(J Clin Res Pediatr Endocrinol 2015; 7: 98-101)

H Syndrome: A Rare Monogenic Cause of Insulin-Dependent Diabetes Mellitus

(J Clin Res Pediatr Endocrinol 2015; 7: 70-70)

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

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

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)

Current Perspectives on Pseudohypoparathyroidism-New Classification

(J Clin Res Pediatr Endocrinol 2016; 8: 1-2)

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)

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)
Turgeon

Marc Olivier Turgeon

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

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

Emin Turkay Korgun

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

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

Alpaslan Kemal Tuzcu

MEN 2A Family

(J Clin Res Pediatr Endocrinol 2017; 9: 22-23)
Tükün

Ajlan Tükün

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

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

Genetic Approach to Thyroid Nodules and Cancer

(J Clin Res Pediatr Endocrinol 2015; 7: 30-30)

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

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

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

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

Leyla Tümer

Investigation of LDLR Gene Mutations in Turkish Patients with Familial Hypercholesterolemia

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

Mehmet Türe

A Case of Odontohypophosphatasia and Family Investigation

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

Özlem Türedi

Three Male Cases with Isodicentric Y Chromosome Mosaicism Including 45,X Cell Line

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

Dilşad Türkdoğan

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

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

Doğa Türkkahraman

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

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

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

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

Mitochondrial ATPase Subunit 6 and Cytochrome B Gene Variations in Obese Turkish Children

(J Clin Res Pediatr Endocrinol 2014; 6: 209-215)

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

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

Letter to the Editor regarding “Testotoxicosis: Report of Two Cases, One with a Novel Mutation in Luteinizing Hormone/Choriogonadotropin Receptor Gene”

(J Clin Res Pediatr Endocrinol 2015; 7: 355-355)

A Novel Null Mutation in P450 Aromatase Gene (CYP19A1) Associated with Development of Hypoplastic Ovaries in Humans

(J Clin Res Pediatr Endocrinol 2016; 8: 205-210)

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)
Türkmen

Mehmet Türkmen

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)

Alpha-Melanocyte-Stimulating Hormone and Agouti-Related Protein: Do They Play a Role in Appetite Regulation in Childhood Obesity?

(J Clin Res Pediatr Endocrinol 2016; 8: 40-47)
Tütüncüler

Filiz Tütüncüler

An Infant with Leydig Cell Hypoplasia Presenting with Bilateral Inguinal Masses

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

Beyhan Tüysüz

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

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

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)

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)

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

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

FGFR2 Gene Mutations in Patients with Syndromic or Isolated Craniosynostosis

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

A Novel Mutation in AMHR2 Gene in Two Siblings with Persistent Müllerian Duct Syndrome

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

Ramkumar TV

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

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