Gonul Aydogan

Istanbul, Turkey

Last Updated: 09/26/2026

Save publications for later

Sign Up

Not sure about your diagnosis?

Check Your Symptoms

Found 37 publications

Evaluation of Optical Coherence Tomography Findings and Choroidal Thickness in Beta-Thalassemia Major Patients Using Chelation Therapy.

Evaluation of Optical Coherence Tomography Findings and Choroidal Thickness in Beta-Thalassemia Major Patients Using Chelation Therapy.

Journal: Beyoglu eye journal

Published: January 02, 2022

Safety and efficacy of deferasirox in patients with transfusion-dependent thalassemia: A 4-year single-center experience.

Safety and efficacy of deferasirox in patients with transfusion-dependent thalassemia: A 4-year single-center experience.

Journal: Pediatric hematology and oncology

Published: March 22, 2021

Clinical Features and Outcome of Children With Hereditary Spherocytosis.

Clinical Features and Outcome of Children With Hereditary Spherocytosis.

Journal: Journal of pediatric hematology/oncology

Published: December 10, 2020

Application of radioisotope synovectomy in the ankle joint in a child with congenital factor VII deficiency.

Application of radioisotope synovectomy in the ankle joint in a child with congenital factor VII deficiency.

Journal: Turk pediatri arsivi

Published: April 07, 2020

Glucose 6 phosphate dehydrogenase deficiency: A single-center experience.

Glucose 6 phosphate dehydrogenase deficiency: A single-center experience.

Journal: Turkish archives of pediatrics

Published: February 13, 2020

A novel mutation in the SLC19A2 gene in a Turkish male with thiamine-responsive megaloblastic anemia syndrome.

A novel mutation in the SLC19A2 gene in a Turkish male with thiamine-responsive megaloblastic anemia syndrome.

Journal: The Turkish journal of pediatrics

Published: January 18, 2020

A novel mutation in the SLC19A2 gene in a Turkish male with thiamine-responsive megaloblastic anemia syndrome.

A novel mutation in the SLC19A2 gene in a Turkish male with thiamine-responsive megaloblastic anemia syndrome.

Journal: The Turkish journal of pediatrics

Published: January 18, 2020

A Pediatric Case of Idiopathic Hypereosinophilia Preceeding Precursor B-cell Lymphoblastic Lymphoma of Nasopharynx.

A Pediatric Case of Idiopathic Hypereosinophilia Preceeding Precursor B-cell Lymphoblastic Lymphoma of Nasopharynx.

Journal: Journal of pediatric hematology/oncology

Published: July 24, 2019

Causes of Hypochromic Microcytic Anemia in Children and Evaluation of Laboratory Parameters in the Differentiation.

Causes of Hypochromic Microcytic Anemia in Children and Evaluation of Laboratory Parameters in the Differentiation.

Journal: Journal of pediatric hematology/oncology

Published: December 18, 2018

Homozygous c.130-131 ins A (pW44X) mutation in the HAX1 gene as the most common cause of congenital neutropenia in Turkey: Report from the Turkish Severe Congenital Neutropenia Registry.

Homozygous c.130-131 ins A (pW44X) mutation in the HAX1 gene as the most common cause of congenital neutropenia in Turkey: Report from the Turkish Severe Congenital Neutropenia Registry.

Journal: Pediatric blood & cancer

Published: November 13, 2018

Deferasirox in children with transfusion-dependent thalassemia or sickle cell anemia: A large cohort real-life experience from Turkey (REACH-THEM).

Deferasirox in children with transfusion-dependent thalassemia or sickle cell anemia: A large cohort real-life experience from Turkey (REACH-THEM).

Journal: European journal of haematology

Published: June 22, 2018

Congenital Factor Deficiencies in Children: A Report of a Single-Center Experience.

Congenital Factor Deficiencies in Children: A Report of a Single-Center Experience.

Journal: Clinical and applied thrombosis/hemostasis : official journal of the International Academy of Clinical and Applied Thrombosis/Hemostasis

Published: October 21, 2017

Showing 1-12 of 37

Last Updated: 09/26/2026