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
Ua-apisitwong

Supoj Ua-apisitwong

Radioactive Iodine for Thyrotoxicosis in Childhood and Adolescence: Treatment and Outcomes

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

Ahmet Uçaktürk

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: -)

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)

VDR Gene Analysis of Four Patients with Hereditary 1,25 Dihydroxyvitamin D-Resistant Rickets

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

A Case of Odontohypophosphatasia and Family Investigation

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

Prevalence of Dyslipidemia and Associated Factors in Obese Children and Adolescents

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

Ahmet Uçar

Is Premature Thelarche in the First Two Years of Life Transient?

(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: -)

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: -)

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)

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

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

Duygu Uçkan

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

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

Vahap Uğurlu

Cellular Trace Element Changes in Type 1 Diabetes Patients

(J Clin Res Pediatr Endocrinol 2016; 8: 180-186)
Ulman

İbrahim Ulman

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

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

Parental View on the Terminology of Disorders of Sex Development

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

Ayça Ulubay

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)
Uluca

Ünal Uluca

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

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

Korkut Ulucan

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: -)

Effect of Cytokine Signaling 3 Gene Polymorphisms in Childhood Obesity

(J Clin Res Pediatr Endocrinol 2016; 8: 452-460)
Uludağ Alkaya

Dilek Uludağ Alkaya

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

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

Selma Ulusal

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)

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

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

Kevalee Unachak

Radioactive Iodine for Thyrotoxicosis in Childhood and Adolescence: Treatment and Outcomes

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

Edip Unal

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

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

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

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

Murat Uncu

The Role of Adenovirus Serotype 36 in Childhood Obesity

(J Clin Res Pediatr Endocrinol 2017; 9: 3-3)
Ungerer

Kobus Ungerer

Patient with Mutation in the Matrix Metalloproteinase 2 (MMP2) Gene - A Case Report and Review of the Literature

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

Tercan Us

Serum Visfatin Levels, Adiposity and Glucose Metabolism in Obese Adolescents

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

Feyza Ustabaş Kahraman

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)
Usui

Takeshi Usui

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

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

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

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

Oya Uyguner

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

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

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)

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

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

Genetics in Pituitary Short Stature

(J Clin Res Pediatr Endocrinol 2015; 7: 35-37)

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

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

Özgün Uygur

The Case of Transient Neonatal Diabetes Mellitus Associated with 6q24

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