AUTHOR INDEX

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Kara

Cengiz Kara

Congenital Goitrous Hypothyroidism, Deafness and Iodide Organification Defect in Four Siblings: Pendred or Pseudo-Pendred Syndrome? - Case Report

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

Etiological Classification and Clinical Assessment of Children and Adolescents with Disorders of Sex Development - Original Article

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

Diabetes Care, Glycemic Control, Complications, and Concomitant Autoimmune Diseases in Children with Type 1 Diabetes in Turkey: A Multicenter Study

(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)

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)

Efficacy and Safety of Sirolimus (mTOR Inhibitor) in Two Patients with Diazoxide-Unresponsive Hyperinsulinemic Hypoglycemia

(J Clin Res Pediatr Endocrinol 2015; 7: 86-86)

Growth Hormone Treatment in an Adolescent with Pycnodysostosis

(J Clin Res Pediatr Endocrinol 2015; 7: 87-87)

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)

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

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

A Case Report of Xp21 Contiguous Gene Syndrome: Adrenal Hypoplasia Congenita, Glycerol Kinase Deficiency, and Duchenne Muscular Dystrophy

(J Clin Res Pediatr Endocrinol 2016; 8: 14-15)

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)

PTPN11, SOS1, and BRAF Gene Mutation Spectrum in RASopathies in Molecular Diagnosis

(J Clin Res Pediatr Endocrinol 2017; 9: 25-25)

Impact of CYP21A2 Gene Mutations on Clinical Management of Congenital Adrenal Hyperplasia

(J Clin Res Pediatr Endocrinol 2017; 9: 25-25)

Williams Syndrome Associated with Isolated Growth Hormone Deficiency: Is It Just a Coincidence?

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

A Rare Cause of Obesity: ROHHAD Syndrome

(J Clin Res Pediatr Endocrinol 2017; 9: 11-11)
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