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
K

Yashaswini K

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

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

Sultan Kaba

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)

Pseudohypoparathyroisidm Type 1a: A Case Report

(J Clin Res Pediatr Endocrinol 2016; 8: 15-15)
Kabakuş

Nimet Kabakuş

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

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

Sema Kabataş Eryılmaz

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

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

Sare Kabukçuoğlu

Gonadoblastoma and Papillary Tubal Hyperplasia in Ovotesticular Disorder of Sexual Development

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

Ayşe Kaçar Bayram

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

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

Ibrahim Kaddam

Prevalence of Vitamin D Deficiency and Calcium Homeostasis in Saudi Children

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

Nikolaos Kadoglou

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

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

Naseebullah Kakar

Two Siblings with Mutation in the Leptin Receptor Gene

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

Kamyar Kalantar-Zadeh

Averting the Legacy of Kidney Disease-Focus on Childhood

(J Clin Res Pediatr Endocrinol 2016; 8: 108-113)
Kamp

Gerdine A. Kamp

Diagnostic Work-up and Follow-up in Children with Tall Stature: A Simplified Algorithm for Clinical Practice

(J Clin Res Pediatr Endocrinol 2015; 7: 260-267)
Kanbur

Nuray Kanbur

An Adolescent Boy with Comorbid Anorexia Nervosa and Hashimoto Thyroiditis

(J Clin Res Pediatr Endocrinol 2016; 8: 92-95)
Kandemir

Nurgün Kandemir

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

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

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: -)

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)
Kandemir

Nurgün Kandemir

Treatment of Growth Hormone Deficiency in Langerhans Cell Histiocytosis

(J Clin Res Pediatr Endocrinol 2015; 7: 21-21)
Kandemir

Nurgün Kandemir

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)

Long-Term Follow-up of a Case with Proprotein Convertase 1/3 Deficiency: Transient Diabetes Mellitus with Intervening Diabetic Ketoacidosis During Growth Hormone Therapy

(J Clin Res Pediatr Endocrinol 2017; 9: 283-287)
Kandiloğlu

Gülşen Kandiloğlu

A Case of Dyskeratosis Congenita Associated with Hypothyroidism and Hypogonadism

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

Saliha Kanık Yüksek

Evaluation of Iodine Deficiency in Children with Attention Deficit/Hyperactivity Disorder

(J Clin Res Pediatr Endocrinol 2016; 8: 61-66)
Kansu

Aydan Kansu

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: -)

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)
Kaplowitz

Paul B. Kaplowitz

Patient Age, Race and the Type of Diabetes Have an Impact on the Presenting Symptoms, Latency Before Diagnosis and Laboratory Abnormalities at Time of Diagnosis of Diabetes Mellitus in Children - Original Article

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

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

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

Sakine Kar

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: -)
Kara

Cengiz Kara

Congenital Goitrous Hypothyroidism, Deafness and Iodide Organification Defect in Four Siblings: Pendred or Pseudo-Pendred Syndrome? - Case Report

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

Etiological Classification and Clinical Assessment of Children and Adolescents with Disorders of Sex Development - Original Article

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

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: -)

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)

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

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

Growth Hormone Treatment in an Adolescent with Pycnodysostosis

(J Clin Res Pediatr Endocrinol 2015; 7: 87-87)

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)

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)

PTPN11, SOS1, and BRAF Gene Mutation Spectrum in RASopathies in Molecular Diagnosis

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

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

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

Williams Syndrome Associated with Isolated Growth Hormone Deficiency: Is It Just a Coincidence?

(J Clin Res Pediatr Endocrinol 2017; 9: 18-18)

A Rare Cause of Obesity: ROHHAD Syndrome

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

The Relationship Between Gestational Diabetes Mellitus and Selenoprotein-P Plasma 1 (SEPP1) Gene Polymorphisms

(J Clin Res Pediatr Endocrinol 2017; 9: 28-28)

Microvascular Complications in Adolescents with Type 1 Diabetes Mellitus

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

Utku Karaarslan

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

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

Halil Gürhan Karabulut

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

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

Emin Karaca

A Case of Dyskeratosis Congenita Associated with Hypothyroidism and Hypogonadism

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

Olfactory Sulcus Hypoplasia Images in a Case of Kallmann Syndrome

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

A Rare GCMB Gene Mutation in an Isolated Hypoparathyroidism Case

(J Clin Res Pediatr Endocrinol 2015; 7: 59-59)

Magnetic Resonance Imaging Characteristics of a Dunnigan-Type Familial Partial Lipodystrophy Patient

(J Clin Res Pediatr Endocrinol 2015; 7: 61-61)

Prevalence and Molecular Characteristics of Y Chromosome Microdeletions in Infertile Males: A Single-Center Study

(J Clin Res Pediatr Endocrinol 2015; 7: 74-74)

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)

Mutation Spectrum of GCK, HNF1A, and HNF1B in MODY Patients and 40 Novel Mutations

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

Fatma Karaca Kara

Prevalence of Dyslipidemia and Associated Factors in Obese Children and Adolescents

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

Mediniye Karadağ Alpaslan

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

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

Ferhan Karademir

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

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

Two Siblings with Mutation in the Leptin Receptor Gene

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

Urinary Netrin-1: A New Biomarker for the Early Diagnosis of Renal Damage in Obese Children

(J Clin Res Pediatr Endocrinol 2016; 8: 282-287)

The Association between Serum 25-Hydroxy Vitamin D Level and Urine Cathelicidin in Children with a Urinary Tract Infection

(J Clin Res Pediatr Endocrinol 2016; 8: 325-329)

POU1F1 and PROP1 Gene Mutations in 4 Cases of Combined Pituitary Hormone Deficiency

(J Clin Res Pediatr Endocrinol 2017; 9: 20-21)
Karadeniz

Cem Karadeniz

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

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

Thyroid Abnormalities in Survivors of Childhood Cancer

(J Clin Res Pediatr Endocrinol 2014; 6: 144-151)
Karaer

Kadri Karaer

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

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

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

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

Düriye Sıla Karagöz Özen

A Rare Genodermatosis: H Syndrome

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

Gülay Karagüzel

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: -)

Cleidocranial Dysplasia: A 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)
Karakaş

Nazmi Mutlu Karakaş

Congenital Hypothyroidism and Bone Remodeling Cycle

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

Sevim Karakaş Çelik

Homozygous Ala65Pro Mutation with V89L Polymorphism in SRD5A2 Deficiency

(J Clin Res Pediatr Endocrinol 2016; 8: 218-223)
Karakoç Aydıner

Elif Karakoç Aydıner

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

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

Musa Karakükçü

Does Early Treatment Prevent Deafness in Thiamine-Responsive Megaloblastic Anaemia Syndrome? - Case Report

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

Ali Karaman

A Rare Genetic Disorder: Partial Trisomy on Chromosome 21

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

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

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

Homozygous SHOX Gene Deletion Detected by Array-CGH in a Girl with Langer Mesomelic Dysplasia

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

Tuba Hilkay Karapınar

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

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

Deniz Karataş

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

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

Noreen Karim

A Novel Missense Mutation in the CLPP Gene Causing Perrault Syndrome Type 3 in a Turkish Family

(J Clin Res Pediatr Endocrinol 2016; 8: 472-477)
Karslıoğlu

Yıldırım Karslıoğlu

Inflammatory Myofibroblastic Tumor Presenting with Diabetes Insipidus in an Eight-Year-Old Boy: A Case Report

(J Clin Res Pediatr Endocrinol 2015; 7: 340-343)
Kartal Baykan

Emine Kartal Baykan

Aromatase Deficiency, a Rare Syndrome: Case Report

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

A Novel Mutation in Deficiency of 11 β-Hydroxylase: A Possible Association with Disease Severity

(J Clin Res Pediatr Endocrinol 2015; 7: 50-50)
Katayıfcı

Nihan Katayıfcı

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)
Katipoğlu

Nagehan Katipoğlu

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

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

Manji Kato

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

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

Walaa E. Kattan

Clinical and Genetic Features of Our Patients with Hypophosphatemic Rickets

(J Clin Res Pediatr Endocrinol 2017; 9: 28-28)
Kavasoğlu

Ayşe Nur Kavasoğlu

A Further Case of Hajdu-Cheney Syndrome Having a Novel Mutation in the NOTCH2 Gene

(J Clin Res Pediatr Endocrinol 2015; 7: 74-74)

Prevalence and Molecular Characteristics of Y Chromosome Microdeletions in Infertile Males: A Single-Center Study

(J Clin Res Pediatr Endocrinol 2015; 7: 74-74)

Six 11-Beta Hydroxylase Deficiency Patients: Identification of Two Novel Mutations

(J Clin Res Pediatr Endocrinol 2017; 9: 26-26)

Anthropometric Measurements and Complications of Achondroplasia Patients

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

Salih Kavukçu

Clinical and Genetic Features of Our Patients with Hypophosphatemic Rickets

(J Clin Res Pediatr Endocrinol 2017; 9: 28-28)
Kavuncuoğlu

Sultan Kavuncuoğlu

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: -)
Kaya

Abdurrahman Kaya

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)

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

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

The First Turkish Case of Hypoparathyroidism, Deafness and Renal Dysplasia (HDR) Syndrome

(J Clin Res Pediatr Endocrinol 2015; 7: 140-143)

Thyroid Hemiagenesis: A Case Report

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

Hypoparathyroidism-Deafness-Renal Disease Syndrome: The First Case Report from Turkey

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

Plasma Kisspeptin Levels in Newborn Infants with Breast Enlargement

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

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)
Kayemba-Kay’s

Simon Kayemba-Kay’s

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)
Kaymaz

Nazan Kaymaz

Isovaleric Acidemia Presenting as Diabetic Ketoacidosis: A Case Report

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

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

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

Hülya Kayserili

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

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

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

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

Bozica Kecman

Early Presentation of Hyperinsulinism/Hyperammonemia Syndrome in Three Serbian Patients

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

Fatma Keklik

Features of Nine Adult Cases of Osteogenesis Imperfecta

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

Sefa Kelekçi

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

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

Ayşenur Keleş

Prepubertal Unilateral Gynecomastia: Report of 2 Cases

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

Fatih Keleşoğlu

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

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

Roya Kelishadi

Association between Obesity and Parental Weight Status in Children and Adolescents

(J Clin Res Pediatr Endocrinol 2017; 9: 111-117)
Kelnar

Chris Kelnar

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

Michaela Kendall

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

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

Yasemin Kendir Demirkol

Different Genotypes in Prader-Willi Syndrome

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

Havva Nur Peltek Kendirci

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: -)

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

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

Familial Glucocorticoid Deficiency Type 2: A Case Report - Case Report

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

Does Early Treatment Prevent Deafness in Thiamine-Responsive Megaloblastic Anaemia Syndrome? - Case Report

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

Vitamin D Deficiency Rickets Mimicking Pseudohypoparathyroidism

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

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

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

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

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

Complex Glycerol Kinase Deficiency and Adrenocortical Insufficiency in Two Neonates

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

Tanıl Kendirli

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

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

ROHHAD Syndrome: Reasons for Diagnostic Difficulties in Obesity

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

Alev Keser

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

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

Halil Keskin

The Effect of Vitamin D Treatment on Serum Adiponectin Levels in Children with Vitamin D Deficiency Rickets - Original Article

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

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

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

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: -)

Increased Resistin Serum Concentrations in Patients with Type 1 Diabetes Mellitus

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

Autoimmune Polyglandular Syndrome Type 3c with Ectodermal Dysplasia, Immune Deficiency and Hemolytic-Uremic Syndrome

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

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)

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)

Case Report of Leri-Weill Dyscontrosteosis Caused By SHOX Gene Deletion

(J Clin Res Pediatr Endocrinol 2017; 9: 14-14)

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)

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: -)

Autoimmune Polyglandular Syndrome Type 3c with Ectodermal Dysplasia, Immune Deficiency and Hemolytic-Uremic Syndrome

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

Bekir Keskinkılıç

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

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

Marion Kessler

Evaluation of Adolescents for Polycystic Ovary Syndrome in an Urban Population - Original Article

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

Nusrat Khan

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

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

Bita Moradi Khaniabadi

Association between Obesity and Parental Weight Status in Children and Adolescents

(J Clin Res Pediatr Endocrinol 2017; 9: 111-117)
Khawash

Papiya Khawash

Nifedipine in Congenital Hyperinsulinism-A Case Report

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

Pooya Khosravi

Different Aspects of Kidney Function in Well-Controlled Congenital Hypothyroidism

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

Ayşe Kılıç

Clinical and Laboratory Characteristics of Children Referred for Early Puberty: Preponderance in 7-8 Years of Age

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

Congenital Goitrous Hypothyroidism, Deafness and Iodide Organification Defect in Four Siblings: Pendred or Pseudo-Pendred Syndrome? - Case Report

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

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

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

Isovaleric Acidemia Presenting as Diabetic Ketoacidosis: A Case Report

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

Increased Thrombin-Activatable Fibrinolysis Inhibitor and Decreased Tissue Factor Pathway Inhibitor and Thrombomodulin Levels in Children with Hypothyroidism

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

M. Arda Kılınç

Autoimmune Polyglandular Syndrome Type 3c with Ectodermal Dysplasia, Immune Deficiency and Hemolytic-Uremic Syndrome

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

Aylin Kılınç Uğurlu

Thyroid Hormone Resistance P453A Mutation

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

Dijle Kıpmen Korgun

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

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

Metin Kır

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

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

Özgür Kırbıyık

A Case with Acrodysostosis and Hormone Resistance

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

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

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

Heves Kırmızıbekmez

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

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

Remission with Cabergoline in Adolescent Boys with Cushing’s Disease

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

Metabolic Bone Disease of Prematurity: Report of Four Cases

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

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

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

Autoimmune Polyglandular Syndrome Type 2: A Rare Condition in Childhood

(J Clin Res Pediatr Endocrinol 2015; 7: 80-82)

A Rare Genetic Disorder: Partial Trisomy on Chromosome 21

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

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

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

A Novel Missense Mutation in the CLPP Gene Causing Perrault Syndrome Type 3 in a Turkish Family

(J Clin Res Pediatr Endocrinol 2016; 8: 472-477)
Kıslal

Fatih Kıslal

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

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

Meltem Kıvılcım

The Effectiveness of Cinacalcet as an Adjunctive Therapy for Hereditary 1,25 Dihydroxyvitamin D3-Resistant Rickets

(J Clin Res Pediatr Endocrinol 2017; 9: 172-178)
Kızılay

Deniz Kızılay

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)

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)
Kızıldağ

Sefa Kızıldağ

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)
Kim

Hyuntae Kim

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

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

A Case of Subclinical Hypothyroidism with Lingual and Right Pretracheal Ectopic Thyroid

(J Clin Res Pediatr Endocrinol 2015; 7: 148-150)

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)
Kiper Mısırlıoğlu

Pınar Kiper Mısırlıoğlu

Mozaic Turner Syndrome and Precocious Puberty Association: A Three-Year-Old Patient

(J Clin Res Pediatr Endocrinol 2015; 7: 58-58)
Kiraz

Aslıhan Kiraz

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: -)

FGFR2 Gene Mutations in Patients with Syndromic or Isolated Craniosynostosis

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

Birgül Kirel

Serum Visfatin Levels, Adiposity and Glucose Metabolism in Obese Adolescents

(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: -)
Kiremitçi

Seniha Kiremitçi

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)
Kitapçı

Ayşın Uçkun Kitapçı

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

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

Ömer Kitiş

Olfactory Sulcus Hypoplasia Images in a Case of Kallmann Syndrome

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

Konstantinos Kitsios

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

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

Julie Tonsgaard Kloppenborg

Subclinical Hypothyroidism in Danish Lean and Obese Children and Adolescents

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

Marie Kmonickova

Normal Bone Turnover in Transient Hyperphosphatasemia

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

Cemile Koca

Evaluation of Asymmetric Dimethylarginine (ADMA) Levels in Children with Growth Hormone Deficiency

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

The Effects of Six-Month L-Thyroxine Treatment on Cognitive Functions and Event-Related Brain Potentials in Children with Subclinical Hypothyroidism

(J Clin Res Pediatr Endocrinol 2015; 7: 102-108)
Kocaay

Pınar Kocaay

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)

A Case of Pycnodysostosis with Bilateral Choanal Atresia

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

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)
Kocaman

Selami Kocaman

Pseudohypoparathyroisidm Type 1a: A Case Report

(J Clin Res Pediatr Endocrinol 2016; 8: 15-15)
Koç Yekedüz

Merve Koç Yekedüz

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)
Koçak

Ülker Koçak

Thyroid Abnormalities in Survivors of Childhood Cancer

(J Clin Res Pediatr Endocrinol 2014; 6: 144-151)
Koçer Gümüşel

Belma Koçer Gümüşel

Urinary Bisphenol A Levels in Girls with Idiopathic Central Precocious Puberty

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

Cemil Koçyiğit

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

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

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)

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

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

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)

Association Between Endocrine Diseases and Serous Otitis Media in Children

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

Mehmet Hanifi Kokaçya

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)
Konak

Belkıs Konak

Anogenital Distance in Turkish Newborns

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

Anogenital Distance in Turkish Newborns

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

Ergun Konakçı

A Comprehensive Online Calculator for Pediatric Endocrinologists: ÇEDD Çözüm/TPEDS Metrics

(J Clin Res Pediatr Endocrinol 2017; 9: 182-184)
Kondolot

Meda Kondolot

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

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

Weight and Height Percentiles For 0-84- Month-Old Children in Kayseri - A Central Anatolian City in Turkey

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

Height, Weight and Body Mass Index Percentiles of Children Aged 6-14 Years Living at Moderate Altitudes

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

Neck Circumference to Assess Obesity in Preschool Children

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

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)
Kondurkar

Shweta Kondurkar

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

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

Petra Konecna

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

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

Young Hwa Kong

A Case of Subclinical Hypothyroidism with Lingual and Right Pretracheal Ectopic Thyroid

(J Clin Res Pediatr Endocrinol 2015; 7: 148-150)
Kor

Yılmaz Kor

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: -)

Autoimmune Polyglandular Syndrome Type 3c with Ectodermal Dysplasia, Immune Deficiency and Hemolytic-Uremic Syndrome

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

Hüseyin Anıl Korkmaz

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

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

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

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

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: -)

Neonatal Seizure as a Manifestation of Unrecognized Maternal Hyperparathyroidism

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

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)

46,XY Complete Gonadal Dysgenesis: A Case Report

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

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

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

A Case with Acrodysostosis and Hormone Resistance

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

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

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

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

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

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)

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

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

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)

Are Vitamin D Drops Containing 400 IU Daily Adequate for Preventing Vitamin D Deficiency?

(J Clin Res Pediatr Endocrinol 2016; 8: 372-372)

A Case of Vanishing Testis Syndrome

(J Clin Res Pediatr Endocrinol 2017; 9: 17-18)

A Case of Marfan Syndrome Presenting with Transverse Striae of the Back

(J Clin Res Pediatr Endocrinol 2017; 9: 14-15)

A Case of Androgen Insensitivity Syndrome Presenting with Micropenis

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

A Novel Mutation in a Patient with 5-α Reductase Deficiency Reared as Girl

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

Heterozygous p.D61G Mutation in a Patient with Noonan Syndrome

(J Clin Res Pediatr Endocrinol 2017; 9: 4-5)

Fetal Adrenal Suppression Due to Maternal Corticosteroid Use: Case Report

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

Congenital Hypothyroidism Due To Maternal Radioactive Iodine Exposure During Pregnancy

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

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)

Maternal Obesity and its Short- and Long-Term Maternal and Infantile Effects

(J Clin Res Pediatr Endocrinol 2016; 8: 114-124)

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

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

A Novel THRA Gene Mutation in Patient with Thyroid Hormone Resistance

(J Clin Res Pediatr Endocrinol 2017; 9: 29-30)

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

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

Sabriye Korkut

Dermal and Ophthalmic Findings in Pseudohypoaldosteronism

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

Complex Glycerol Kinase Deficiency and Adrenocortical Insufficiency in Two Neonates

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

Katarzyna Korzeniowska

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: -)
Kosta

Konstantina Kosta

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

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

Celalettin Koşan

Cystinosis Presenting with Findings of Bartter Syndrome - Case Report

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

L. Damla Kotan

Distribution of Gene Mutations Associated with Familial Normosmic Idiopathic Hypogonadotropic Hypogonadism

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

Idiopathic Hypogonadotrophic Hypogonadism Caused by Inactivating Mutations in SRA1

(J Clin Res Pediatr Endocrinol 2016; 8: 17-17)

Idiopathic Hypogonadotropic Hypogonadism Caused by Inactivating Mutations in SRA1

(J Clin Res Pediatr Endocrinol 2016; 8: 125-134)

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)
Koyuncuoğlu Güngör

Neslihan Koyuncuoğlu Güngör

Overweight and Obesity in Children and Adolescents

(J Clin Res Pediatr Endocrinol 2014; 6: 129-143)
Köker

Sultan Aydın Köker

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

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

Esad Köklü

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

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

Rıza Köksal Özgül

Isovaleric Acidemia Presenting as Diabetic Ketoacidosis: A Case Report

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

Yılmaz Kör

Increased Resistin Serum Concentrations in Patients with Type 1 Diabetes Mellitus

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

Sezen Köse

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

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

Muhammet Köşker

Prevalence of Metabolic Syndrome in Obese Children and Adolescents using Three Different Criteria and Evaluation of Risk Factors - Original Article

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

Cem Köz

Cardiac Autonomic Functions in Obese Children - Original Article

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

Pieta Krijnen

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

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

Nils Krone

17-Hydroxylase Deficiency: Rare Cause of Delayed Puberty

(J Clin Res Pediatr Endocrinol 2017; 9: 26-26)
KS

Shivaprasad KS

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

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

Ayşe Kubat Kuruüzüm

Familial Partial Lipodystrophy Linked to aNovel Peroxisome Proliferator-Activated Receptor -γ (PPARG) Mutation, H449L

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

Ayşe Kubat Üzüm

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)
Kucur

Mine Kucur

Vitamin D Deficiency and Hashimoto’s Thyroiditis in Children and Adolescents: a Critical Vitamin D Level for This Association?

(J Clin Res Pediatr Endocrinol 2015; 7: 128-133)

The Relationship of Disordered Eating Attitudes with Stress Level, Bone Turnover Markers, and Bone Mineral Density in Obese Adolescents

(J Clin Res Pediatr Endocrinol 2017; 9: 237-245)
Kul

Mustafa Kul

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)
Kuloğlu

Zarife Kuloğlu

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)
Kumanov

Philip Kumanov

Prevalence of Cryptorchidism Among Bulgarian Boys - Original Article

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

Anıl Kumar

Patient Age, Race and the Type of Diabetes Have an Impact on the Presenting Symptoms, Latency Before Diagnosis and Laboratory Abnormalities at Time of Diagnosis of Diabetes Mellitus in Children - Original Article

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

Monogenic Diabetes Secondary to Congenital Lipodystrophy in a 14-year-old Yemeni Girl-Case Report

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

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: -)
Kurku

Hüseyin Kurku

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

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

Erdal Kurnaz

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)
Kurt

Yasemin Gülcan Kurt

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)
Kurtbay

Yaşar Bekir Kurtbay

The Mutation Spectrum of DHCR7 Gene and Two Novel Mutations

(J Clin Res Pediatr Endocrinol 2017; 9: 21-22)
Kurtoğlu

Selim Kurtoğlu

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

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

Therapeutic Approach to Obesity in Children and Adolescents

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

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

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

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

Melnick-Needles Syndrome Associated with Growth Hormone Deficiency: A Case Report - Case Report

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

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

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

Iodine Overload and Severe Hypothyroidism in Two Neonates - Case Report

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

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: -)

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

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

Familial Glucocorticoid Deficiency Type 2: A Case Report - Case Report

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

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

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

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: -)

Does Early Treatment Prevent Deafness in Thiamine-Responsive Megaloblastic Anaemia Syndrome? - Case Report

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

Fetal Adrenal Suppression Due to Maternal Corticosteroid Use: Case Report

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

Vitamin D Deficiency Rickets Mimicking Pseudohypoparathyroidism

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

Weight and Height Percentiles For 0-84- Month-Old Children in Kayseri - A Central Anatolian City in Turkey

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

Follow-Up During Early Infancy of Newborns Diagnosed with Subcutaneous Fat Necrosis

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

Association Between Apolipoprotein E Polymorphism and Subclinic Atherosclerosis in Patients with Type 1 Diabetes Mellitus

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

Height, Weight and Body Mass Index Percentiles of Children Aged 6-14 Years Living at Moderate Altitudes

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

Congenital Hypothyroidism Due To Maternal Radioactive Iodine Exposure During Pregnancy

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

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

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

Anthropometric Studies on the Turkish 
Population - A Historical Review

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

Micropenis: Etiology, Diagnosis and Treatment Approaches

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

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

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

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)

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

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

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)

Dermal and Ophthalmic Findings in Pseudohypoaldosteronism

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

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

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

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

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

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

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

Maternal Obesity and its Short- and Long-Term Maternal and Infantile Effects

(J Clin Res Pediatr Endocrinol 2016; 8: 114-124)

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

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

Complex Glycerol Kinase Deficiency and Adrenocortical Insufficiency in Two Neonates

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

Non-Classical Congenital Adrenal Hyperplasia in Childhood

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

Neck Circumference to Assess Obesity in Preschool Children

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

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)
Kuru Pekcan

Meryem Kuru Pekcan

Role of Versican and ADAMTS-1 in Polycystic Ovary Syndrome

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

Barış Kuşkonmaz

Hyperthyroidism After Allogeneic Hematopoietic Stem Cell Transplantation: A Report of Four Cases

(J Clin Res Pediatr Endocrinol 2015; 7: 349-354)
Kutilek

Stepan Kutilek

Normal Bone Turnover in Transient Hyperphosphatasemia

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

Alev Oğuz Kutlu

Normative Data for Penile Length in Turkish Newborns - Original Article

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

Anogenital Distance in Turkish Newborns

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

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)
Kutlu Yaman

Arzu Kutlu Yaman

Maternal and Neonatal Urinary Iodine Status and its Effect on Neonatal TSH Levels in a Mildly Iodine-Deficient Area

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

Suat Hayri Küçük

Vitamin D Deficiency in Children and Adolescents in Bağcılar, İstanbul

(J Clin Res Pediatr Endocrinol 2015; 7: 134-139)
Küçük Kurtulgan

Hande Küçük Kurtulgan

8Q22.3-Q24.23 Duplication: A Case Report

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

Banu Küçükemre Aydın

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

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

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

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

Clinical and Laboratory Characteristics of Children Referred for Early Puberty: Preponderance in 7-8 Years of Age

(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)

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)
Küme

Tuncay Küme

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

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