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Korkmaz

Hüseyin Anıl Korkmaz

Hypochondroplasia in a Child with 1620C>G (Asn540Lys) Mutation in FGFR3

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

A Case of Turner Syndrome with Concomitant 
Transient Hypogammaglobulinaemia of 
Infancy and Central Diabetes Insipidus

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

Impact of Insulin Resistance on Insulin-Like Growth Factor-1/Insulin Like Growth Factor-Binding Protein-3 Axis and on Early Weight Gain in Small for Gestational Age Infants

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

Neonatal Seizure as a Manifestation of Unrecognized Maternal Hyperparathyroidism

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

Investigation of Genes That are Defined with New Generation Sequence Analysis in Children/Adolescents Followed with Maturity Onset Diabetes of the Young

(J Clin Res Pediatr Endocrinol 2015; 7: 46-46)

46,XY Complete Gonadal Dysgenesis: A Case Report

(J Clin Res Pediatr Endocrinol 2015; 7: 65-65)

Screening of PROP-1, LHX2, and POU1F1 Mutations in Patients with Ectopic Posterior Pituitary Gland

(J Clin Res Pediatr Endocrinol 2015; 7: 65-65)

A Case with Acrodysostosis and Hormone Resistance

(J Clin Res Pediatr Endocrinol 2015; 7: 75-75)

Genetic Diagnosis Using Whole Exome Analysis in Two Cases with Malignant Infantile Osteopetrosis

(J Clin Res Pediatr Endocrinol 2015; 7: 76-76)

Genotype-Phenotype Correlation of Congenital Adrenal Hyperplasia Cases Having Complex (Multiple) Mutation Detected in CYP21A2 Gene

(J Clin Res Pediatr Endocrinol 2015; 7: 88-88)

A Case with Infantile-Onset Pancytopenia and Hyperglycemia Associated with SLC19A2 Mutation

(J Clin Res Pediatr Endocrinol 2015; 7: 89-89)

Factors Influencing Serum Vitamin D Concentration in Turkish Children Residing in İzmir: A Single-Center Experience

(J Clin Res Pediatr Endocrinol 2015; 7: 294-300)

Genetic Diagnosis Using Whole Exome Analysis in Two Cases with Malignant Osteopetrosis of Infancy

(J Clin Res Pediatr Endocrinol 2015; 7: 356-357)

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)

Are Vitamin D Drops Containing 400 IU Daily Adequate for Preventing Vitamin D Deficiency?

(J Clin Res Pediatr Endocrinol 2016; 8: 372-372)

A Case of Vanishing Testis Syndrome

(J Clin Res Pediatr Endocrinol 2017; 9: 17-18)

A Case of Marfan Syndrome Presenting with Transverse Striae of the Back

(J Clin Res Pediatr Endocrinol 2017; 9: 14-15)

A Case of Androgen Insensitivity Syndrome Presenting with Micropenis

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

A Novel Mutation in a Patient with 5-α Reductase Deficiency Reared as Girl

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

Heterozygous p.D61G Mutation in a Patient with Noonan Syndrome

(J Clin Res Pediatr Endocrinol 2017; 9: 4-5)
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