AUTHOR INDEX

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Güven

Ayla Güven

Association Between the Corrected QT Interval and Carotid Artery Intima-Media Thickness in Obese Children - Original Article

(J Clin Res Pediatr Endocrinol 2010; 2: -)

3M Syndrome: A Report of Four Cases in Two Families

(J Clin Res Pediatr Endocrinol 2011; 3: -)

Delirium in Diabetic Ketoacidosis: A Case Report

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

Developmental Defects of the Thyroid Gland: Relationship with Advanced Maternal Age

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

Distribution of Gene Mutations Associated with Familial Normosmic Idiopathic Hypogonadotropic Hypogonadism

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

Profile of Hypothyroidism in Down’s Syndrome

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

Remission with Cabergoline in Adolescent Boys with Cushing’s Disease

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

Mutant Neurogenin-3 in Permanent Neonatal Diabetes and Congenital Malabsorptive Diarrhea

(J Clin Res Pediatr Endocrinol 2015; 7: 10-10)

Current Practice in Diagnosis and Treatment of Growth Hormone Deficiency in Childhood: A Survey from Turkey

(J Clin Res Pediatr Endocrinol 2015; 7: 37-44)

Seven Cases of Williams-Beuren Syndrome: Endocrine Evaluation and Long-Term Follow-Up

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

Assessment of Anti-Müllerian Hormone Level in Management of Adolescents with Polycystic Ovary Syndrome

(J Clin Res Pediatr Endocrinol 2016; 8: 55-60)

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 Diabetic Infant with Homozygous LRBA Mutation: The Youngest Patient Reported

(J Clin Res Pediatr Endocrinol 2016; 8: 16-16)

The Growth Characteristics of Patients with Noonan Syndrome: Results of Three Years of Growth Hormone Treatment: A Nationwide Multicenter Study

(J Clin Res Pediatr Endocrinol 2016; 8: 305-312)

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)

17-Hydroxylase Deficiency: Rare Cause of Delayed Puberty

(J Clin Res Pediatr Endocrinol 2017; 9: 26-26)

Warburg Micro Syndrome: A New Case from Consanguineous Parents

(J Clin Res Pediatr Endocrinol 2017; 9: 18-18)

CYP11A1 Mutations Result in Various Clinical Phenotypes

(J Clin Res Pediatr Endocrinol 2017; 9: 2-3)
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