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Rational use of chronic graft-versus-host treatment alternatives: A systematic review

Transfusion and apheresis science, 2022-02, Vol.61 (1), p.103371-103371, Article 103371

2022

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Is Sickle Cell Trait Really Innocent?

Turkish journal of haematology, 2021-06, Vol.38 (2), p.159-160

2021

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Comparison of the clinical course of COVID-19 infection in sickle cell disease patients with healthcare professionals

Annals of hematology, 2021-09, Vol.100 (9), p.2195-2202

2021

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What the Largest Earthquake in 100 Years Has Taught Us: Real-Life Data from a JACIE-Accredited Bone Marrow Transplant Center

Turkish journal of haematology, 2023-05, Vol.40 (2), p.130-131

2023

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Use of Plerixafor to Mobilize a Healthy Donor Infected with Influenza A

Turkish journal of haematology, 2018-05, Vol.35 (2), p.138-139

2018

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An Unusual Giant Leg Ulcer as a Rare Presentation of Sweet's Syndrome in a Patient with Hairy Cell Leukemia Successfully Managed by Splenectomy

Turkish journal of haematology, 2017-09, Vol.34 (3), p.270-281

2017

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Hematopoietic Stem Cell Transplantation in Adult Sickle Cell Disease: Problems and Solutions

Turkish journal of haematology, 2015-09, Vol.32 (3), p.195-205

2015

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Clinical significance of circulating blood and endothelial cell microparticles in sickle-cell disease

Journal of thrombosis and thrombolysis, 2014, Vol.38 (2), p.167-175

2014

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An Approach to Pediatric or Mentally Deficient Donors from a Bioethical Perspective: Considerations and Recommendations on Behalf of the Donor Research Team of the Turkish Society of Hematology (DART)

Turkish journal of haematology, 2022-01, Vol.39 (3), p.220-221

2022

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Effectiveness of Visual Methods in Information Procedures for Stem Cell Recipients and Donors

Turkish journal of haematology, 2017-12, Vol.34 (4), p.321-327

2017

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Demodicidosis Accompanying Acute Cutaneous Graft-Versus-Host Disease after Allogeneic Stem Cell Transplantation

Turkish journal of haematology, 2018, Vol.35 (4), p.313-314

2018

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Tacrolimus-induced diabetic ketoacidosis after allogeneic bone marrow transplant

Experimental and clinical transplantation, 2017-12, Vol.15 (6), p.702-703

2017

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Role of prophylactic and therapeutic red blood cell exchange in pregnancy with sickle cell disease: Maternal and perinatal outcomes

Journal of clinical apheresis, 2021-06, Vol.36 (3), p.283-290

2021

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Is the Game Over or Starting Again? The Role of the Transplant Team in Genetic Counseling for Adult Sickle Cell Disease Recipients

Turkish journal of haematology, 2017-06, Vol.34 (2), p.196-197

2017

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The Clinicopathologic Features and the Factors Associated with the Survival in Light -Chain Amyloidosis Patients: A Single Center Descriptive Study

Medical journal of Bakirköy, 2020

2020

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Frequency of Finding Family Donors: A Single Center Experience

Experimental and clinical transplantation, 2018-03, Vol.16 Suppl 1 (Suppl 1), p.47-50

2018

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Anorectal Complications During Neutropenic Period in Patients with Hematologic Diseases

Mediterranean journal of hematology and infectious diseases, 2016-03, Vol.8 (1), p.e2016019-e2016019

2016

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Effect of Hereditary Hemochromatosis Gene H63D and C282Y Mutations on Iron Overload in Sickle Cell Disease Patients

Turkish journal of haematology, 2016-12, Vol.33 (4), p.320-325

2016

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A rare hematological complication of visceral leishmaniasis: hemophagocytic syndrome

Çukurova Üniversitesi tip fakültesi dergisi, 2016-01, Vol.41 (1), p.161

2016

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A Rare Complication Developing After Hematopoietic Stem Cell Transplantation: Wernicke's Encephalopathy

Turkish journal of haematology, 2015-12, Vol.32 (4), p.367-370

2015

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Implementation of an ISBT 128-Compatible Medical Record System to Facilitate Traceability of Stem Cell Products

Turkish journal of haematology, 2017-08, Vol.34 (3), p.280-281

2017

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Cobalamin Deficiency Can Mask Depleted Body Iron Reserves

Indian journal of hematology & blood transfusion, 2015-06, Vol.31 (2), p.255-258

2015

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Use of mesenchymal cells to modulate immune suppression and immune reconstruction in a patient with aplastic anemia complicated by invasive sino-orbital aspergillosis

Turkish journal of haematology, 2014-06, Vol.31 (2), p.181-183

2014

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Recommendations for Risk Categorization and Prophylaxis of Invasive Fungal Diseases in Hematological Malignancies: A Critical Review of Evidence and Expert Opinion (TEO-4)

Turkish journal of haematology, 2015-06, Vol.32 (2), p.100-117

2015

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Tunnelled central venous catheter-related problems in the early phase of haematopoietic stem cell transplantation and effects on transplant outcome

Turkish journal of haematology, 2015-03, Vol.32 (1), p.51-57

2015

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Rational use of chronic graft-versus-host treatment alternatives: A systematic review

Is Sickle Cell Trait Really Innocent?

Comparison of the clinical course of COVID-19 infection in sickle cell disease patients with healthcare professionals

What the Largest Earthquake in 100 Years Has Taught Us: Real-Life Data from a JACIE-Accredited Bone Marrow Transplant Center

Use of Plerixafor to Mobilize a Healthy Donor Infected with Influenza A

An Unusual Giant Leg Ulcer as a Rare Presentation of Sweet's Syndrome in a Patient with Hairy Cell Leukemia Successfully Managed by Splenectomy

Hematopoietic Stem Cell Transplantation in Adult Sickle Cell Disease: Problems and Solutions

Clinical significance of circulating blood and endothelial cell microparticles in sickle-cell disease

An Approach to Pediatric or Mentally Deficient Donors from a Bioethical Perspective: Considerations and Recommendations on Behalf of the Donor Research Team of the Turkish Society of Hematology (DART)

Effectiveness of Visual Methods in Information Procedures for Stem Cell Recipients and Donors

Demodicidosis Accompanying Acute Cutaneous Graft-Versus-Host Disease after Allogeneic Stem Cell Transplantation

Tacrolimus-induced diabetic ketoacidosis after allogeneic bone marrow transplant

Role of prophylactic and therapeutic red blood cell exchange in pregnancy with sickle cell disease: Maternal and perinatal outcomes

Is the Game Over or Starting Again? The Role of the Transplant Team in Genetic Counseling for Adult Sickle Cell Disease Recipients

The Clinicopathologic Features and the Factors Associated with the Survival in Light -Chain Amyloidosis Patients: A Single Center Descriptive Study

Frequency of Finding Family Donors: A Single Center Experience

Anorectal Complications During Neutropenic Period in Patients with Hematologic Diseases

Effect of Hereditary Hemochromatosis Gene H63D and C282Y Mutations on Iron Overload in Sickle Cell Disease Patients

A rare hematological complication of visceral leishmaniasis: hemophagocytic syndrome

A Rare Complication Developing After Hematopoietic Stem Cell Transplantation: Wernicke's Encephalopathy

Implementation of an ISBT 128-Compatible Medical Record System to Facilitate Traceability of Stem Cell Products

Cobalamin Deficiency Can Mask Depleted Body Iron Reserves

Use of mesenchymal cells to modulate immune suppression and immune reconstruction in a patient with aplastic anemia complicated by invasive sino-orbital aspergillosis

Recommendations for Risk Categorization and Prophylaxis of Invasive Fungal Diseases in Hematological Malignancies: A Critical Review of Evidence and Expert Opinion (TEO-4)

Tunnelled central venous catheter-related problems in the early phase of haematopoietic stem cell transplantation and effects on transplant outcome

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