Turkiz Gursel

The Prevalence, Risk Factors and Cardiometabolic Complications of Obesity in Childhood Survivors of Acute Lymphoblastic Leukemia.

Journal: Indian journal of hematology & blood transfusion : an official journal of Indian Society of Hematology and Blood Transfusion

Published: January 03, 2023

Inherited coagulation disorders in Turkish children: A retrospective, single-center cohort study.

Journal: Transfusion and apheresis science : official journal of the World Apheresis Association : official journal of the European Society for Haemapheresis

Published: November 02, 2019

Hematologic Findings of Inherited Metabolic Disease: They are More Than Expected.

Journal: Journal of pediatric hematology/oncology

Published: May 11, 2018

Association of CYP3A5 Expression and Vincristine Neurotoxicity in Pediatric Malignancies in Turkish Population.

Journal: Journal of pediatric hematology/oncology

Published: July 12, 2017

Successful total hip replacement with sequential administration of bypassing agents in an adolescent boy with hemophilia A and high inhibitor titers.

Journal: Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis

Published: January 13, 2017

The effect of CYP2C9 and VKORC1 genetic polymorphisms on warfarin dose requirements in a pediatric population.

Journal: Anatolian journal of cardiology

Published: May 17, 2016

Influence of Folate-Related Gene Polymorphisms on High-Dose Methotrexate-Related Toxicity and Prognosis in Turkish Children with Acute Lymphoblastic Leukemia.

Journal: Turkish journal of haematology : official journal of Turkish Society of Haematology

Published: April 21, 2016

Transcobalamin II Deficiency in Four Cases with Novel Mutations.

Journal: Turkish journal of haematology : official journal of Turkish Society of Haematology

Published: April 28, 2015

Prognostic Factors and Long-Term Outcome in 52 Turkish Children With Hemophagocytic Lymphohistiocytosis.

Journal: Pediatric critical care medicine : a journal of the Society of Critical Care Medicine and the World Federation of Pediatric Intensive and Critical Care Societies

Published: April 23, 2015

Severe Myelotoxicity Associated with Thiopurine S-Methyltransferase3A/3C Polymorphisms in a Patient with Pediatric Leukemia and the Effect of Steroid Therapy.

Journal: Turkish journal of haematology : official journal of Turkish Society of Haematology

Published: December 27, 2014

The Prevalence, Risk Factors and Cardiometabolic Complications of Obesity in Childhood Survivors of Acute Lymphoblastic Leukemia.

The Prevalence, Risk Factors and Cardiometabolic Complications of Obesity in Childhood Survivors of Acute Lymphoblastic Leukemia.

Inherited coagulation disorders in Turkish children: A retrospective, single-center cohort study.

Inherited coagulation disorders in Turkish children: A retrospective, single-center cohort study.

Hematologic Findings of Inherited Metabolic Disease: They are More Than Expected.

Hematologic Findings of Inherited Metabolic Disease: They are More Than Expected.

Association of CYP3A5 Expression and Vincristine Neurotoxicity in Pediatric Malignancies in Turkish Population.

Association of CYP3A5 Expression and Vincristine Neurotoxicity in Pediatric Malignancies in Turkish Population.

Successful total hip replacement with sequential administration of bypassing agents in an adolescent boy with hemophilia A and high inhibitor titers.

Successful total hip replacement with sequential administration of bypassing agents in an adolescent boy with hemophilia A and high inhibitor titers.

The effect of CYP2C9 and VKORC1 genetic polymorphisms on warfarin dose requirements in a pediatric population.

The effect of CYP2C9 and VKORC1 genetic polymorphisms on warfarin dose requirements in a pediatric population.

Influence of Folate-Related Gene Polymorphisms on High-Dose Methotrexate-Related Toxicity and Prognosis in Turkish Children with Acute Lymphoblastic Leukemia.

Influence of Folate-Related Gene Polymorphisms on High-Dose Methotrexate-Related Toxicity and Prognosis in Turkish Children with Acute Lymphoblastic Leukemia.

Transcobalamin II Deficiency in Four Cases with Novel Mutations.

Transcobalamin II Deficiency in Four Cases with Novel Mutations.

Prognostic Factors and Long-Term Outcome in 52 Turkish Children With Hemophagocytic Lymphohistiocytosis.

Prognostic Factors and Long-Term Outcome in 52 Turkish Children With Hemophagocytic Lymphohistiocytosis.

Severe Myelotoxicity Associated with Thiopurine S-Methyltransferase3A/3C Polymorphisms in a Patient with Pediatric Leukemia and the Effect of Steroid Therapy.

Severe Myelotoxicity Associated with Thiopurine S-Methyltransferase3A/3C Polymorphisms in a Patient with Pediatric Leukemia and the Effect of Steroid Therapy.

Recombinant long-acting glycoPEGylated factor IX in hemophilia B: a multinational randomized phase 3 trial.

Recombinant long-acting glycoPEGylated factor IX in hemophilia B: a multinational randomized phase 3 trial.

Molecular basis and bleeding manifestations of factor XI deficiency in 11 Turkish families.

Molecular basis and bleeding manifestations of factor XI deficiency in 11 Turkish families.

Turkiz Gursel

The Prevalence, Risk Factors and Cardiometabolic Complications of Obesity in Childhood Survivors of Acute Lymphoblastic Leukemia.

The Prevalence, Risk Factors and Cardiometabolic Complications of Obesity in Childhood Survivors of Acute Lymphoblastic Leukemia.

Inherited coagulation disorders in Turkish children: A retrospective, single-center cohort study.

Inherited coagulation disorders in Turkish children: A retrospective, single-center cohort study.

Hematologic Findings of Inherited Metabolic Disease: They are More Than Expected.

Hematologic Findings of Inherited Metabolic Disease: They are More Than Expected.

Association of CYP3A5 Expression and Vincristine Neurotoxicity in Pediatric Malignancies in Turkish Population.

Association of CYP3A5 Expression and Vincristine Neurotoxicity in Pediatric Malignancies in Turkish Population.

Successful total hip replacement with sequential administration of bypassing agents in an adolescent boy with hemophilia A and high inhibitor titers.

Successful total hip replacement with sequential administration of bypassing agents in an adolescent boy with hemophilia A and high inhibitor titers.

The effect of CYP2C9 and VKORC1 genetic polymorphisms on warfarin dose requirements in a pediatric population.

The effect of CYP2C9 and VKORC1 genetic polymorphisms on warfarin dose requirements in a pediatric population.

Influence of Folate-Related Gene Polymorphisms on High-Dose Methotrexate-Related Toxicity and Prognosis in Turkish Children with Acute Lymphoblastic Leukemia.

Influence of Folate-Related Gene Polymorphisms on High-Dose Methotrexate-Related Toxicity and Prognosis in Turkish Children with Acute Lymphoblastic Leukemia.

Transcobalamin II Deficiency in Four Cases with Novel Mutations.

Transcobalamin II Deficiency in Four Cases with Novel Mutations.

Prognostic Factors and Long-Term Outcome in 52 Turkish Children With Hemophagocytic Lymphohistiocytosis.

Prognostic Factors and Long-Term Outcome in 52 Turkish Children With Hemophagocytic Lymphohistiocytosis.

Severe Myelotoxicity Associated with Thiopurine S-Methyltransferase*3A/*3C Polymorphisms in a Patient with Pediatric Leukemia and the Effect of Steroid Therapy.

Severe Myelotoxicity Associated with Thiopurine S-Methyltransferase*3A/*3C Polymorphisms in a Patient with Pediatric Leukemia and the Effect of Steroid Therapy.

Recombinant long-acting glycoPEGylated factor IX in hemophilia B: a multinational randomized phase 3 trial.

Recombinant long-acting glycoPEGylated factor IX in hemophilia B: a multinational randomized phase 3 trial.

Molecular basis and bleeding manifestations of factor XI deficiency in 11 Turkish families.

Molecular basis and bleeding manifestations of factor XI deficiency in 11 Turkish families.

Severe Myelotoxicity Associated with Thiopurine S-Methyltransferase3A/3C Polymorphisms in a Patient with Pediatric Leukemia and the Effect of Steroid Therapy.

Severe Myelotoxicity Associated with Thiopurine S-Methyltransferase3A/3C Polymorphisms in a Patient with Pediatric Leukemia and the Effect of Steroid Therapy.