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
Ünal

Sevim Ünal

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)
Ünal Kocabaş

Gökçen Ünal Kocabaş

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

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

Gözde Ünek

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

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

Emin Ünüvar

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

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

Fetal and Neonatal Endocrine Disruptors

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

The Role of Initial Clinical and Laboratory Findings in Infants With Hyperthyrotropinemia to Predict Transient or Permanent Hypothyroidism

(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)

An Early Spontaneous Recovery in a Hyperinsulinemia and Hypoglycemia Case with a Recently Found Mutation on the Gene ABCC8

(J Clin Res Pediatr Endocrinol 2015; 7: 47-47)

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)
Ünver Tuhan

Hale Ünver Tuhan

The Effect of L-Thyroxine Treatment on Hypothyroid Symptom Scores and Lipid Profile in Children with Subclinical Hypothyroidism

(J Clin Res Pediatr Endocrinol 2014; 6: 238-244)

Recovery of Central Fever after GH Therapy in a Patient with GH Deficiency Secondary to Posttraumatic Brain Injury

(J Clin Res Pediatr Endocrinol 2015; 7: 77-79)

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)

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)

Neonatal Diabetes Mellitus due to a Novel Mutation in the GATA6 Gene Accompanying Renal Dysfunction: A Case Report

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

A Case of Achondrogenesis Type 2/Hypochondrogenesis Due to a De Novo Mutation in the COL2A1 Gene

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

Duran Üstek

A Homozygous Nonsense Thyroid Peroxidase Mutation (R540X) Consistently Causes Congenital Hypothyroidism in Two Siblings Born to a Consanguineous Family

(J Clin Res Pediatr Endocrinol 2015; 7: 323-328)
Üstün

Melek Üstün

Gonadoblastoma and Papillary Tubal Hyperplasia in Ovotesticular Disorder of Sexual Development

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

Selin Üstün Bezgin

Association Between Endocrine Diseases and Serous Otitis Media in Children

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

H. Bahri Üstünbaş

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: -)

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

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

Ala Üstyol

Corticosterone Methyl Oxidase Deficiency Type 1 with Normokalemia in an Infant

(J Clin Res Pediatr Endocrinol 2016; 8: 356-359)
Home Archive Search Menu