2016 8 June (6) 2
Journal citation Report 2016
Substantial Informations
ENDO 2016
ECE 2016
ECO 2016
ESPE 2016
EASAD 2016
ISPAD 2016

Editor’s Note

Editor’s Note

(J Clin Res Pediatr Endocrinol 2016; 8: 0-0)


Maternal Obesity and its Short- and Long-Term Maternal and Infantile Effects

(J Clin Res Pediatr Endocrinol 2016; 8: 114-124)

Original Article

Idiopathic Hypogonadotropic Hypogonadism Caused by Inactivating Mutations in SRA1

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

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

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

Investigation of SHOX Gene Mutations in Turkish Patients with Idiopathic Short Stature

(J Clin Res Pediatr Endocrinol 2016; 8: 144-149)

Effects of Thyroid Autoimmunity on Early Atherosclerosis in Euthyroid Girls with Hashimoto’s Thyroiditis

(J Clin Res Pediatr Endocrinol 2016; 8: 150-156)

Thyroid Function and Thyroid Autoimmunity in Relation to Weight Status and Cardiovascular Risk Factors in Children and Adolescents: A Population-Based Study

(J Clin Res Pediatr Endocrinol 2016; 8: 157-162)

Bone Mineral Density in Adolescent Girls with Hypogonadotropic and Hypergonadotropic Hypogonadism

(J Clin Res Pediatr Endocrinol 2016; 8: 163-169)

Transient Congenital Hypothyroidism in Turkey: An Analysis on Frequency and Natural Course

(J Clin Res Pediatr Endocrinol 2016; 8: 170-179)

Cellular Trace Element Changes in Type 1 Diabetes Patients

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

Neonatal Thyroid-Stimulating Hormone Screening as a Monitoring Tool for Iodine Deficiency in Turkey

(J Clin Res Pediatr Endocrinol 2016; 8: 187-191)

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

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

Clinical and Genetic Characteristics, Management and Long-Term Follow-Up of Turkish Patients with Congenital Hyperinsulinism

(J Clin Res Pediatr Endocrinol 2016; 8: 197-204)

A Novel Null Mutation in P450 Aromatase Gene (CYP19A1) Associated with Development of Hypoplastic Ovaries in Humans

(J Clin Res Pediatr Endocrinol 2016; 8: 205-210)

Gonadotropin-Releasing Hormone Analogue Treatment in Females with Moderately Early Puberty: No Effect on Final Height

(J Clin Res Pediatr Endocrinol 2016; 8: 211-217)

Homozygous Ala65Pro Mutation with V89L Polymorphism in SRD5A2 Deficiency

(J Clin Res Pediatr Endocrinol 2016; 8: 218-223)

Case Report

A Novel c.554+5C>T Mutation in the DUOXA2 Gene Combined with p.R885Q Mutation in the DUOX2 Gene Causing Congenital Hypothyroidism

(J Clin Res Pediatr Endocrinol 2016; 8: 224-227)

Early Presentation of Hyperinsulinism/Hyperammonemia Syndrome in Three Serbian Patients

(J Clin Res Pediatr Endocrinol 2016; 8: 228-231)

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)

Phenotype, Sex of Rearing, Gender Re-Assignment, and Response to Medical Treatment in Extended Family Members with a Novel Mutation in the SRD5A2 Gene

(J Clin Res Pediatr Endocrinol 2016; 8: 236-240)

A Novel Mutation in Thyroid Peroxidase Gene Causing Congenital Goitrous Hypothyroidism in a German-Thai Patient

(J Clin Res Pediatr Endocrinol 2016; 8: 241-245)

A Newly-Discovered Mutation in the RFX6 Gene of the Rare Mitchell-Riley Syndrome

(J Clin Res Pediatr Endocrinol 2016; 8: 246-249)

Long-term Outcome after Robotic-assisted Gastroplication in Adolescents: Hunger Hormone and Food Preference Changes Two Case Reports

(J Clin Res Pediatr Endocrinol 2016; 8: 250-256)
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