Sema Aylan Gelen

Management of Hyperleukocytosis in Childhood Acute Leukemia Without Leukapheresis and Rasburicase Prophylaxis

N. Sarper, E. Zengin, Sema Aylan Gelen, 2021, Journal of pediatric hematology/oncology.

Thrombolysis with Systemic Recombinant Tissue Plasminogen Activator in Children: A Multicenter Retrospective Study

Y. Oymak, H. Ören, H. Gülen, 2021, Turkish journal of haematology : official journal of Turkish Society of Haematology.

The Association of Oral Vitamin D and Calcium Supplementation With Bone Mineral Density in Pediatric Acute Lymphoblastic Leukemia Patients

H. Demir, T. Kum, N. Sarper, 2017, Journal of pediatric hematology/oncology.

Screening Bleeding Disorders in Adolescents and Young Women with Menorrhagia

N. Sarper, E. Zengin, Sema Aylan Gelen, 2013, Turkish journal of haematology : official journal of Turkish Society of Haematology.

Induction Deaths and Treatment-Related Mortality in Childhood Acute Lymphoblastic Leukemia with ALL-BFM Protocols

N. Sarper, E. Zengin, Sema Aylan Gelen, 2021 .

Prognostic evidence of LEF1 isoforms in childhood acute lymphoblastic leukemia

Ozden Hatirnaz Ng, U. Ozbek, I. Can, 2021, International journal of laboratory hematology.

Clinical Characteristics of Pediatric Patients with Congenital Erythrocytosis: A Single-Center Study

N. Sarper, E. Zengin, Sema Aylan Gelen, 2021, Indian Journal of Hematology and Blood Transfusion.

High Infection-Related Mortality in Pediatric Acute Myeloid Leukemia without Preventive Antibiotics and Antifungals: Retrospective Cohort Study of a Single Center from a Middle-Income Country

D. Dündar, S. Öncel, N. Sarper, 2017, Turkish journal of haematology : official journal of Turkish Society of Haematology.

Posterior reversible encephalopathy syndrome related to COVID-19 in a child.

Sema Aylan Gelen, G. Arslan, T. Besci, 2022, Pediatrics international : official journal of the Japan Pediatric Society.

Autoimmune Hemolytic Anemia Due to Spondyloenchondrodysplasia with Spastic Paraparesis and Intracranial Calcification due to Mutation in ACP5

B. Kara, N. Sarper, E. Zengin, 2021, Journal of Pediatric Genetics.