Search Results - "Erer, Buket"
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Effects of iron overload and hepatitis C virus positivity in determining progression of liver fibrosis in thalassemia following bone marrow transplantation
Published in Blood (01-07-2002)“…To identify the role of iron overload in the natural history of liver fibrosis, we reviewed serial hepatic biopsy specimens taken annually from patients cured…”
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The effects of mesenchymal stem cells on lymphoblastic leukemia cell proliferation
Published in Journal of B.U. ON. (01-10-2014)“…Mesenchymal stem cells (MSCs) represent a new approach to the treatment of several neoplastic or non-neoplastic disorders. Their potential to repair damaged…”
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Purified T-depleted, CD34+ peripheral blood and bone marrow cell transplantation from haploidentical mother to child with thalassemia
Published in Blood (11-02-2010)“…Fetomaternal microchimerism suggests immunological tolerance between mother and fetus. Thus, we performed primary hematopoietic stem cell transplantation from…”
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New approach for bone marrow transplantation in patients with class 3 thalassemia aged younger than 17 years
Published in Blood (15-08-2004)“…When prepared for transplantation with busulfan (BU) 14 mg/kg and cyclophosphamide (CY) 120 to 160 mg/kg, patients with thalassemia in risk class 3, aged…”
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Phlebotomy to reduce iron overload in patients cured of thalassemia by bone marrow transplantation
Published in Blood (01-08-1997)“…Abstract In thalassemia after successful bone marrow transplantation (BMT), iron overload remains an important cause of morbidity. After BMT, patients have…”
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Preliminary Experience of the Pakistani Network for the Cure and Prevention of Thalassaemia Supported by the Cure2Children Foundation
Published in Blood (20-11-2009)“…Abstract 4331 Since May 2008, the Cure2Children Foundation has supported both financially and professionally a network of centers in Pakistan for stem cell…”
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Bone Marrow Transplantation in Thalassemia: The Experience of Pesaro
Published in Annals of the New York Academy of Sciences (01-06-1998)“…: Early trials of allogenic bone marrow transplantation (BMT) for homozygous β thalassemia and the analyses of results of transplantation in patients under 17…”
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Early T Cell Recovery of Thymus-Derived Naive T Cells and NK Cells in Pediatrics Patients after T-Cell Depleted HLA-Haploidentical Stem Cell Transplantation for Thalassemia
Published in Blood (16-11-2007)“…Delayed immune recovery post transplant remains a significant obstacle and results in increased risk of infections. T cells are regenerated via 2 pathway,…”
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Purified T Depleted Peripheral Blood and Bone Marrow Cd34 Transplantation from Haploidentical Mother to Child with Thalassemia
Published in Blood (16-11-2006)“…Approximately 60% of thalassemic patients can not apply to “gene therapy today” which the insertion of one allogenic HLA identical stem cell into the empty…”
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Long-Term Outcome after Bone Marrow Transplantation for Adult Thalassemia
Published in Blood (16-11-2005)“…Advances in management of thalassemia have increased the proportion of patients living into adulthood. However, disease and treatment related complications in…”
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Immuno Haematological Reconstitution after T-Cell-Depleted HLA-Haploidentical Stem Cell Transplantation for Thalassemia
Published in Blood (16-11-2006)“…Background. We evaluated haematological and immunological characteristics of four thalassemia patients after T-cell-depleted HLA-haploidentical stem cell…”
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Stem cell transplantation from HLA‐matched related donor for Fanconi's anaemia: a retrospective review of the multicentric Italian experience on behalf of Associazione Italiana di Ematologia ed Oncologia Pediatrica (AIEOP)–Gruppo Italiano Trapianto di Midollo Osseo (GITMO)
Published in British journal of haematology (01-03-2001)“…Twenty‐seven consecutive Italian patients with Fanconi's anaemia (FA) underwent stem cell transplantation (SCT) from an HLA‐matched related donor in 10 Italian…”
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Phlebotomy to Reduce Iron Overload in Patients Cured of Thalassemia by Bone Marrow Transplantation
Published in Blood (01-08-1997)“…In thalassemia after successful bone marrow transplantation (BMT), iron overload remains an important cause of morbidity. After BMT, patients have normal…”
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Graft-versus-host disease after bone marrow transplantation for thalassemia : An analysis of incidence and risk factors
Published in Transplantation (27-03-1997)“…We analyzed risk factors in 724 patients evaluable for acute graft-versus-host disease (GVHD) and in 614 patients evaluable for chronic GVHD who had received…”
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Treatment of Iron Overload in the "Ex-Thalassemic": Report from the Phlebotomy Program
Published in Annals of the New York Academy of Sciences (30-06-1998)“…After successful marrow transplantation (BMT) iron overload remains an important cause of morbidity in Thalassemia. After BMT, patients have normal…”
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Immunohematologic Reconstitution in Pediatric Patients after T Cell-Depleted HLA-Haploidentical Stem Cell Transplantation for Thalassemia
Published in Biology of blood and marrow transplantation (01-11-2010)“…To analyze immunohematologic reconstitution, particularly of natural killer (NK) cells, we evaluated 13 β-thalassemia patients after 20 and 60 days and 1 year…”
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GRAFT-VERSUS-HOST DISEASE AFTER BONE MARROW TRANSPLANTATION FOR THALASSEMIA: AN ANALYSIS OF INCIDENCE AND RISK FACTORS1
Published in Transplantation (01-03-1997)Get full text
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Treatment of Iron Overload in the “Ex‐Thalassemic”: Report from the Phlebotomy Programa
Published in Annals of the New York Academy of Sciences (01-06-1998)“…: After successful marrow transplantation (BMT) iron overload remains an important cause of morbidity in Thalassemia. After BMT, patients have normal…”
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