2017-9-9-3
2017 9 September (9) 3
JCRPE - ScholarOne
Substantial Informations
Journal citation Report 2016
Usage of ORCID
Sci-Expanded
Pubmed/Medline
ESPE 2017
ISPAD 2017

Original Article

Clinicopathological Characteristics of Papillary Thyroid Cancer in Children with Emphasis on Pubertal Status and Association with BRAFV600E Mutation

(J Clin Res Pediatr Endocrinol 2017; 9: 185-193)

Congenital Hyperinsulinism in China: A Review of Chinese Literature Over the Past 15 Years

(J Clin Res Pediatr Endocrinol 2017; 9: 194-201)

The Relationship Between Glycemic Variability and Inflammatory Markers in Obese Children with Insulin Resistance and Metabolic Syndrome

(J Clin Res Pediatr Endocrinol 2017; 9: 202-207)

Treatment of Pre-pubertal Patients with Growth Hormone Deficiency: Patterns in Growth Hormone Dosage and Insulin-like Growth Factor-I Z-scores

(J Clin Res Pediatr Endocrinol 2017; 9: 208-215)

Melanocortin-4 Receptor Gene Mutations in a Group of Turkish Obese Children and Adolescents

(J Clin Res Pediatr Endocrinol 2017; 9: 216-221)

Management of Childhood Thyroid Nodules: Surgical and Endocrinological Findings in a Large Group of Cases

(J Clin Res Pediatr Endocrinol 2017; 9: 222-228)

Clinical and Genetic Findings of Turkish Hypophosphatasia Cases

(J Clin Res Pediatr Endocrinol 2017; 9: 229-236)

The Relationship of Disordered Eating Attitudes with Stress Level, Bone Turnover Markers, and Bone Mineral Density in Obese Adolescents

(J Clin Res Pediatr Endocrinol 2017; 9: 237-245)

Phenotype Heterogeneity in Glucokinase–Maturity-Onset Diabetes of the Young (GCK-MODY) Patients

(J Clin Res Pediatr Endocrinol 2017; 9: 246-252)

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)

Short Communication

An ABCC8 Nonsense Mutation Causing Neonatal Diabetes Through Altered Transcript Expression

(J Clin Res Pediatr Endocrinol 2017; 9: 260-264)

Case Report

Pituitary Adenoma Apoplexy in an Adolescent: A Case Report and Review of the Literature

(J Clin Res Pediatr Endocrinol 2017; 9: 265-273)

Pancreatic Agenesis due to Compound Heterozygosity for a Novel Enhancer and Truncating Mutation in the PTF1A Gene

(J Clin Res Pediatr Endocrinol 2017; 9: 274-277)

Congenital Central Hypothyroidism Caused by a Novel Thyroid-Stimulating Hormone-Beta Subunit Gene Mutation in Two Siblings

(J Clin Res Pediatr Endocrinol 2017; 9: 278-282)

Long-Term Follow-up of a Case with Proprotein Convertase 1/3 Deficiency: Transient Diabetes Mellitus with Intervening Diabetic Ketoacidosis During Growth Hormone Therapy

(J Clin Res Pediatr Endocrinol 2017; 9: 283-287)

Tolvaptan Treatment in Children with Chronic Hyponatremia due to Inappropriate Antidiuretic Hormone Secretion: A Report of Three Cases

(J Clin Res Pediatr Endocrinol 2017; 9: 288-292)
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