Ali Ocheltree

Metabolic Control in Children and Adolescents with Insulin-Dependent Diabetes Mellitus at King Abdul-Aziz University Hospital

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

Sevinç Odabaşı Güneş

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)

Gönül Oğur

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 Male Case of Aromatase Deficiency with a Novel CYP19A1 Mutation

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

Aynur Oğuz

Thyroid Abnormalities in Survivors of Childhood Cancer

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

Menstrual Characteristics of Pubertal Girls: A Questionnaire-Based Study in Turkey

(J Clin Res Pediatr Endocrinol 2016; 8: 192-196)

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

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

Sibel Oğuzkan Balcı

The Possible Role of Mitochondrial Uncoupling Protein 2 (UCP2) Gene on the Development of Metabolic Syndrome and Platelet Count in Obese Children/Adolescents - A Preliminary Study

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

A Preliminary Study of the Possible Role of Cannabinoid Receptor-1 (CNR1) Gene Polymorphisms in the Development of Morbid Obesity in Obese Children

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

Johanne Dam Ohrt

Subclinical Hypothyroidism in Danish Lean and Obese Children and Adolescents

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

Mehmet Okan

Resolution of Autoimmune Oophoritis after Thymectomy in a Myasthenia Gravis Patient

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

Deniz Okdemir

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

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

Hiroaki Okuno

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

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

Arzu Okur

Thyroid Abnormalities in Survivors of Childhood Cancer

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

Cleidocranial Dysplasia: A Case Report

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

Investigation of LDLR Gene Mutations in Turkish Patients with Familial Hypercholesterolemia

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

Nihal Olgaç Dündar

Adipokines in Breast Milk: An Update

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

Stacy R. Oliver

Inflammatory Cytokine Profiles During Exercise in Obese, Diabetic, and Healthy Children

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

Anjumanara Omar

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: -)

Tülay Omma

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

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

Sertaç Hanedan Onan

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: -)

Hüseyin Onay

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

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

Diabetes and Our Genes

(J Clin Res Pediatr Endocrinol 2015; 7: 25-25)

Melanocortin-4 Receptor Mutation and Obesity

(J Clin Res Pediatr Endocrinol 2015; 7: 43-43)

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)

A New Mutation on the SFR1 (NR5A1) Gene in a 46 XY Sexual Development Disorder Case without the Adrenal Deficiency

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

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

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

Genetic Analysis of Lipodystrophies and Recently Found Mutations

(J Clin Res Pediatr Endocrinol 2015; 7: 63-63)

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)

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

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

Growth Hormone Treatment in an Adolescent with Pycnodysostosis

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

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)

Genetic Analysis of Lipodystrophies and Novel Mutations

(J Clin Res Pediatr Endocrinol 2015; 7: 90-90)

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)

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

(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)

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

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

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)

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

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

Investigation of Androgen Receptor Gen Mutation Spectrum in the Turkish Patients with Disorder of Sex Development

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

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

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

Anthropometric Measurements and Complications of Achondroplasia Patients

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

The Mutation Spectrum of DHCR7 Gene and Two Novel Mutations

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

FGFR2 Gene Mutations in Patients with Syndromic or Isolated Craniosynostosis

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

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

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

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

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

HOXC4 Gene is Possibly Responsible for Lin-Gettig Syndrome

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

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

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

Atypical LMNA Mutation in EXON 11 Associated with a Milder Clinical Outcome in Dunnigan-Type Familial Partial Lipodystrophy

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

Two Cases of Testicular Adrenal Rest Tumor (TART)

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

A Case of MEN 2A: D631Y Mutation

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

Two Cases of Klinefelter Syndrome

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

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

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

Sena Kara Oncu

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: -)

Kristin S. Ondrak

Interrelationships Among Changes in Leptin, Insulin, Cortisol and Growth Hormone and Weight Status in Youth - Original Article

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

Wilma Oostdijk

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

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

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

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

Bülent Oran

Atherogenic Lipid Profile and Systolic Blood Pressure are Associated with Carotid Artery Intima-media Thickness in Children with Turner Syndrome - Original Article

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

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

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

Zerrin Orbak

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)

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)

Plasma Kisspeptin Levels in Newborn Infants with Breast Enlargement

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

Çiğdem Oruç

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)

Jennifer Osei

Breast-Milk Iodine Concentrations, Iodine Status, and Thyroid Function of Breastfed Infants Aged 2-4 Months and Their Mothers Residing in a South African Township

(J Clin Res Pediatr Endocrinol 2016; 8: 381-391)

Yongri Ouyang

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

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

Pembe Oygar

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

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

Yeşim Oymak

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

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

Keeichi Ozono

Progeroid Syndrome Patients with ZMPSTE24 Deficiency Could Benefit When Treated with Rapamycin and Dimethylsulfoxide

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