2017-3-9-1
2017 9 March (3) 1
Journal citation Report 2016
Substantial Informations
Sci-Expanded
Pubmed/Medline
ENDO 2017
ECE 2017
ECO 2017
ESPE 2017
ISPAD 2017

Review

Non-Classical Congenital Adrenal Hyperplasia in Childhood

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

Original Article

Subclinical Hypothyroidism in Danish Lean and Obese Children and Adolescents

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

Neck Circumference to Assess Obesity in Preschool Children

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

Role of Versican and ADAMTS-1 in Polycystic Ovary Syndrome

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

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

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

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)

Association Between Endocrine Diseases and Serous Otitis Media in Children

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

Clinical and Mutational Features of Three Chinese Children with Congenital Generalized Lipodystrophy

(J Clin Res Pediatr Endocrinol 2017; 9: 52-57)

Age-Specific Frequencies and Characteristics of Ovarian Cysts in Children and Adolescents

(J Clin Res Pediatr Endocrinol 2017; 9: 58-62)

Safety and Efficacy of Stosstherapy in Nutritional Rickets

(J Clin Res Pediatr Endocrinol 2017; 9: 63-69)

Case Report

Uniparental Isodisomy of Chromosome 1 Unmasking an Autosomal Recessive 3-Beta Hydroxysteroid Dehydrogenase Type II-Related Congenital Adrenal Hyperplasia

(J Clin Res Pediatr Endocrinol 2017; 9: 70-73)

Follow-up Findings in a Turkish Girl with Pseudohypoparathyroidism Type Ia Caused by a Novel Heterozygous Mutation in the GNAS Gene

(J Clin Res Pediatr Endocrinol 2017; 9: 74-79)

Clinical and Molecular Genetic Analysis in Three Children with Wolfram Syndrome: A Novel WFS1 Mutation (c.2534T>A)

(J Clin Res Pediatr Endocrinol 2017; 9: 80-84)

Testicular Adrenal Rest Tumor in Two Brothers with a Novel Mutation in the 3-Beta-Hydroxysteroid Dehydrogenase-2 Gene

(J Clin Res Pediatr Endocrinol 2017; 9: 85-90)

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)
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