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
Yadav

Charu Yadav

Indices of Glucose Homeostasis in Cord Blood in Term and Preterm Newborns

(J Clin Res Pediatr Endocrinol 2016; 8: 270-275)
Yağmurlu

Aydın Yağmurlu

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: -)
Yakut

Halil İbrahim Yakut

Role of Versican and ADAMTS-1 in Polycystic Ovary Syndrome

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

A Case of Odontohypophosphatasia and Family Investigation

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

Mehmet Yalan

The Case of Transient Neonatal Diabetes Mellitus Associated with 6q24

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

Mehmet Yalaz

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

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

Koray Yalçın

Recognizing the Psychosocial Aspects of Type 1 Diabetes in Adolescents

(J Clin Res Pediatr Endocrinol 2015; 7: 57-62)
Yalın

Gülşah Y. Yalın

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

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

Betül Yaman

Growth Hormone Therapy in Five Patients with Malignant Intracranial Tumors

(J Clin Res Pediatr Endocrinol 2015; 7: 9-9)

A Case of Polyglandular Autoimmune Syndrome Type One with Hypercalcemia and Hypotension

(J Clin Res Pediatr Endocrinol 2015; 7: 51-51)
Yang

Hua Yang

Association between Common Genetic Variants and Polycystic Ovary Syndrome Risk in a Chinese Han Population

(J Clin Res Pediatr Endocrinol 2016; 8: 405-410)

Low-Grade Inflammation and Increased Arterial Stiffness in Chinese Youth and Adolescents with Newly-Diagnosed Type 2 Diabetes Mellitus

(J Clin Res Pediatr Endocrinol 2015; 7: 268-273)

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

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

Şenay Yapıcı

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

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

Sema Yarman

Familial Acromegaly

(J Clin Res Pediatr Endocrinol 2015; 7: 34-34)
Yavaş Abalı

Zehra Yavaş Abalı

Long-term Endocrine Evaluation of Childhood Brain Tumors

(J Clin Res Pediatr Endocrinol 2015; 7: 22-22)

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)

A Critical Appraisal of Growth Hormone Therapy in Growth Hormone Deficiency and Turner Syndrome Patients in Turkey

(J Clin Res Pediatr Endocrinol 2016; 8: 490-495)
Yazıcı

Ayşe Canan Yazıcı

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

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

Olcay Yeğin

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

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

Ensar Yekeler

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

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

Arda Yel

Diabetic Ketoacidosis Presenting with Pseudonormoglycemia in a 15-Year-Old Girl with Type 1 Diabetes Mellitus

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

Pseudohypoparathyroisidm Type 1a: A Case Report

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

Gülşah Yenidünya Yalın

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

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

Gözde Yeşil

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: -)
Yeşilkaya

Ediz Yeşilkaya

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

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

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: -)

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)

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)

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)

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)

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)

Effect of Cytokine Signaling 3 Gene Polymorphisms in Childhood Obesity

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

Gül Yeşiltepe Mutlu

Vitamin D Deficiency in Children and Adolescents with Type 1 Diabetes

(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: -)

Features of Two Cases with 18q Deletion Syndrome

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

Metabolic Bone Disease of Prematurity: Report of Four Cases

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

Ring Chromosome 13 and Ambiguous Genitalia

(J Clin Res Pediatr Endocrinol 2014; 6: 122-124)

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)

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)

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

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

Is Hyperpigmentation on the First Day of Life Always Associated with IMAGe Syndrome?

(J Clin Res Pediatr Endocrinol 2014; 6: 266-268)

Autoimmune Polyglandular Syndrome Type 2: A Rare Condition in Childhood

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

Hakkı Yeşilyurt

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

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

Aylin Yetim

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)

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)
Yeung

Matthew Chun-wing Yeung

Corticosterone Methyl Oxidase Deficiency Type 1 with Normokalemia in an Infant

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

Ali Yıkılmaz

Neonatal Sludge: A finding of congenital hypothyroidism - Case Report

(J Clin Res Pediatr Endocrinol 2009; 1: 197-200)

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)
Yıldırım

Nurdan Yıldırım

Insulin Oedema in Newly Diagnosed Type 1 Diabetes Mellitus - Case Report

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

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 Case of Thyroid Hormone Resistance

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

Complete Androgen Insensitivity Syndrome; the Importance of Family Screening

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

Association of Subclinical Hypothyroidism with Dyslipidemia and Increased Carotid Intima-Media Thickness in Children

(J Clin Res Pediatr Endocrinol 2017; 9: 144-149)

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

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

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

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

Ilgın Yıldırım Şimşir

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)

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

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

Heterozygous AGPAT2 Mutation, Diabetes, and Lipodystrophy in Extremities

(J Clin Res Pediatr Endocrinol 2015; 7: 53-53)
Yıldırımer

Ülkü Yıldırımer

Diabetic Ketoacidosis Presenting with Pseudonormoglycemia in a 15-Year-Old Girl with Type 1 Diabetes Mellitus

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

Aysel Yıldız

Vitamin D Deficiency Rickets Mimicking Pseudohypoparathyroidism

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

A Randomized Clinical Trial Comparing Breakfast and Bedtime Administration of Insulin Glargine in Children and Adolescents with Type 1 Diabetes - Original Article

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

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

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

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)

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)

Association Between Endocrine Diseases and Serous Otitis Media in Children

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

Complementary and Alternative Medicine in Children with Type 1 Diabetes Mellitus

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

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

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

Profile of Hypothyroidism in Down’s Syndrome

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

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

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

Alev Yılmaz

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

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

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

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

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)

Heterozygous AGPAT2 Mutation, Diabetes, and Lipodystrophy in Extremities

(J Clin Res Pediatr Endocrinol 2015; 7: 53-53)

Editorial

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

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)

Growth Hormone Treatment in an Adolescent with Pycnodysostosis

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

Relationship Between Aspartate Aminotransferase-to-Platelet Ratio Index and Carotid Intima-Media Thickness in Obese Adolescents with Non-Alcoholic Fatty Liver Disease

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

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

(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)

Pseudohypoparathyroidism Presenting with Ventricular Arrhythmia: A Case Report

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

Distribution of RET Mutations and Evaluation of Treatment Approaches in Hereditary Medullary Thyroid Carcinoma in Turkey

(J Clin Res Pediatr Endocrinol 2016; 8: 13-20)

Role of Versican and ADAMTS-1 in Polycystic Ovary Syndrome

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

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

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

Congenital Hypothyroidism Due To Maternal Radioactive Iodine Exposure During Pregnancy

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

Constitutional Growth Delay Pattern of Growth in Velo-Cardio-Facial Syndrome: Longitudinal follow up and final height of two cases - Case Report

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

Sebahat Yılmaz Ağladıoğlu

Does Pseudohypoaldosteronism Mask the Diagnosis of Congenital Adrenal Hyperplasia?

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

Sebahat Yılmaz Ağladıoğlu

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: -)

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: -)
Yılmaz Yalçın

Yaprak Yılmaz Yalçın

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

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

Murat Muhtar Yılmazer

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

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

Özgül Yiğit

Vitamin D Deficiency in Children and Adolescents in Bağcılar, İstanbul

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

İsmail Yildiz

Association of Subclinical Hypothyroidism with Dyslipidemia and Increased Carotid Intima-Media Thickness in Children

(J Clin Res Pediatr Endocrinol 2017; 9: 144-149)
Yokuşoğlu

Mehmet Yokuşoğlu

Cardiac Autonomic Functions in Obese Children - Original Article

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

Jong Seo Yoon

Luteinizing Hormone Secretion during Gonadotropin-Releasing Hormone Stimulation Tests in Obese Girls with Central Precocious Puberty

(J Clin Res Pediatr Endocrinol 2016; 8: 392-398)
Yorulmaz

Alaaddin Yorulmaz

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)
Yozgat

Yılmaz Yozgat

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

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

Göze Yörük

Educational Needs of Adolescents Regarding Normal Puberty and Menstrual Patterns

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

Yi Yuan

Association between Common Genetic Variants and Polycystic Ovary Syndrome Risk in a Chinese Han Population

(J Clin Res Pediatr Endocrinol 2016; 8: 405-410)
Yuca

Sevil Arı Yuca

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

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

Zoe Yung

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

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

Özge Yüce

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)

A Hypogonadotropic Hypogonadism Case as a Consequence of GNRHR Mutation

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

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)
Yüceer

Nurullah Yüceer

A Case of Central Precocious Puberty Due to Concomitant Hypothalamic Hamartoma and Juvenile Pilocytic Astrocytoma

(J Clin Res Pediatr Endocrinol 2014; 6: 183-186)
Yüksel

Ayşegül Yüksel

Genetic Analysis in Our Cases with Thyroid Dysgenesis

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

Distribution of RET Mutations and Evaluation of Treatment Approaches in Hereditary Medullary Thyroid Carcinoma in Turkey

(J Clin Res Pediatr Endocrinol 2016; 8: 13-20)

Evaluation of Permanent Growth Hormone Deficiency (GHD) in Young Adults with Childhood Onset GHD: A multicenter study - Original Article

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

Neuroendocrinological Control of Obesity

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

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: -)

Distribution of Gene Mutations Associated with Familial Normosmic Idiopathic Hypogonadotropic Hypogonadism

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

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

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

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

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

Coexistence of Kabuki Syndrome and Autoimmune Thyroiditis

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

Crouzon Syndrome with Hypoplasia of Corpus Callosum and Inferior Vermis

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

Wolcott-Rallison Syndrome

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

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

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

Coexistence of Kabuki Syndrome and Autoimmune Thyroiditis

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

Idiopathic Hypogonadotropic Hypogonadism Caused by Inactivating Mutations in SRA1

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

Idiopathic Hypogonadotrophic Hypogonadism Caused by Inactivating Mutations in SRA1

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

Crouzonodermoskeletal Syndrome with Hypoplasia of Corpus Callosum and Inferior Vermis

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

Wolcott-Rallison Syndrome with Novel EIF2AK3 Gene Mutation

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

Hypogonadotropic Hypogonadism due to Novel FGFR1 Mutations

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

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

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

Özge Özalp Yüreğir

Coexistence of Kabuki Syndrome and Autoimmune Thyroiditis

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

Banu Şarer Yürekli

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)

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)

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

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

Zeynep Yürük Yıldırım

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

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