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Optimal Outcomes in Young Class 3 Patients With Thalassemia Undergoing HLA-Identical Sibling Bone Marrow Transplantation

Transplantation, 2016-04, Vol.100 (4), p.925-932

2016

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Bone marrow transplantation for thalassemia from alternative related donors: improved outcomes with a new approach

Blood, 2013-10, Vol.122 (15), p.2751-2756

2013

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Purified T-depleted, CD34+ peripheral blood and bone marrow cell transplantation from haploidentical mother to child with thalassemia

Blood, 2010-02, Vol.115 (6), p.1296-1302

2010

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Spirometric Evaluation of Pulmonary Function in Nigerian Children underwent Bone Marrow Transplantation for Sickle Cell Anemia

Mediterranean journal of hematology and infectious diseases, 2017, Vol.9 (1), p.e2017030-e2017030

2017

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T-cell homeostasis alteration in HIV-1 infected subjects with low CD4 T-cell count despite undetectable virus load during HAART

AIDS (London), 2006-10, Vol.20 (16), p.2033-2041

2006

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Altered Clonogenic Capability and Stromal Cell Function Characterize Bone Marrow of HIV-Infected Subjects with Low CD4+ T Cell Counts Despite Viral Suppression during HAART

Clinical infectious diseases, 2008-06, Vol.46 (12), p.1902-1910

2008

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Hematopoietic stem cell transplantation in thalassemia and sickle cell anemia

Cold Spring Harbor perspectives in medicine, 2012-05, Vol.2 (5), p.a011825-a011825

2012

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New insights into the pharmacokinetics of intravenous busulfan in children with sickle cell anemia undergoing bone marrow transplantation

Pediatric blood & cancer, 2015-04, Vol.62 (4), p.680-686

2015

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Bone Marrow Clonogenic Capability, Cytokine Production, and Thymic Output in Patients with Common Variable Immunodeficiency

The Journal of immunology (1950), 2005-04, Vol.174 (8), p.5074-5081

2005

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Busulfan–fludarabine- or treosulfan–fludarabine-based myeloablative conditioning for children with thalassemia major

Annals of hematology, 2022-03, Vol.101 (3), p.655-665

2022

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Progress in hematopoietic stem cell transplantation as allogeneic cellular gene therapy in thalassemia

Annals of the New York Academy of Sciences, 2010-08, Vol.1202 (1), p.149-154

2010

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Posterior Reversible Encephalopathy Syndrome after Hematopoietic Cell Transplantation in Children with Hemoglobinopathies

Biology of blood and marrow transplantation, 2017-09, Vol.23 (9), p.1531-1540

2017

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One single bone marrow harvesting from donors under 3 years of age: assessing safety and efficacy of the procedure

Bone marrow transplantation (Basingstoke), 2019-07, Vol.54 (7), p.1121-1123

2019

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Successes and pitfalls in orphan drug development for sickle cell disease

Blood advances, 2024-05, Vol.8 (10), p.2455-2465

2024

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Immunodysregulation of HIV disease at bone marrow level

Autoimmunity reviews, 2005-11, Vol.4 (8), p.486-490

2005

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T cell-depleted hla-haploidentical stem cell transplantation in thalassemia young patients

Pediatric reports, 2011-06, Vol.3 Suppl 2 (12), p.e13-e13

2011

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Invasive pulmonary aspergillosis in a haematopoietic stem cell transplant recipient with sickle cell disease: a successful treatment

Mediterranean journal of hematology and infectious diseases, 2015, Vol.7 (1), p.e2015006

2015

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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

Blood, 2007-11, Vol.110 (11), p.3816-3816

2007

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Histological features of bone marrow in paediatric patients during the asymptomatic phase of early-stage Black African sickle cell anaemia

Pathology, 2017-04, Vol.49 (3), p.297-303

2017

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Haploidentical HSCT for hemoglobinopathies: improved outcomes with TCRαβ+/CD19+-depleted grafts

Blood advances, 2018-02, Vol.2 (3), p.263-270

2018

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Outcomes of Unrelated Bone Marrow Transplantation in Patients with Thalassemia

Blood, 2018-11, Vol.132 (Supplement 1), p.5777-5777

2018

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Late-Onset Hemorrhagic Cystitis in Children after Hematopoietic Stem Cell Transplantation for Thalassemia and Sickle Cell Anemia: A Prospective Evaluation of Polyoma (BK) Virus Infection and Treatment with Cidofovir

Biology of blood and marrow transplantation, 2010-05, Vol.16 (5), p.662-671

2010

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Optimal Outcomes in Young Class 3 Patients With Thalassemia Undergoing HLA-Identical Sibling Bone Marrow Transplantation

Bone marrow transplantation for thalassemia from alternative related donors: improved outcomes with a new approach

Novel pharmacokinetic behavior of intravenous busulfan in children with thalassemia undergoing hematopoietic stem cell transplantation: a prospective evaluation of pharmacokinetic and pharmacodynamic profile with therapeutic drug monitoring

Purified T-depleted, CD34+ peripheral blood and bone marrow cell transplantation from haploidentical mother to child with thalassemia

Spirometric Evaluation of Pulmonary Function in Nigerian Children underwent Bone Marrow Transplantation for Sickle Cell Anemia

T-cell homeostasis alteration in HIV-1 infected subjects with low CD4 T-cell count despite undetectable virus load during HAART

Altered Clonogenic Capability and Stromal Cell Function Characterize Bone Marrow of HIV-Infected Subjects with Low CD4+ T Cell Counts Despite Viral Suppression during HAART

Hematopoietic stem cell transplantation in thalassemia and sickle cell anemia

New insights into the pharmacokinetics of intravenous busulfan in children with sickle cell anemia undergoing bone marrow transplantation

Bone Marrow Clonogenic Capability, Cytokine Production, and Thymic Output in Patients with Common Variable Immunodeficiency

Busulfan–fludarabine- or treosulfan–fludarabine-based myeloablative conditioning for children with thalassemia major

Progress in hematopoietic stem cell transplantation as allogeneic cellular gene therapy in thalassemia

Posterior Reversible Encephalopathy Syndrome after Hematopoietic Cell Transplantation in Children with Hemoglobinopathies

One single bone marrow harvesting from donors under 3 years of age: assessing safety and efficacy of the procedure

Successes and pitfalls in orphan drug development for sickle cell disease

Immunodysregulation of HIV disease at bone marrow level

T cell-depleted hla-haploidentical stem cell transplantation in thalassemia young patients

Invasive pulmonary aspergillosis in a haematopoietic stem cell transplant recipient with sickle cell disease: a successful treatment

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

Histological features of bone marrow in paediatric patients during the asymptomatic phase of early-stage Black African sickle cell anaemia

Busulfan-fludarabine- or treosulfan-fludarabine-based conditioning before allogeneic HSCT from matched sibling donors in paediatric patients with sickle cell disease: A study on behalf of the EBMT Paediatric Diseases and Inborn Errors Working Parties

Haploidentical HSCT for hemoglobinopathies: improved outcomes with TCRαβ+/CD19+-depleted grafts

Outcomes of Unrelated Bone Marrow Transplantation in Patients with Thalassemia

Outcomes of allogeneic haematopoietic cell transplantation for myelofibrosis in children and adolescents: the retrospective study of the EBMT Paediatric Diseases WP

Late-Onset Hemorrhagic Cystitis in Children after Hematopoietic Stem Cell Transplantation for Thalassemia and Sickle Cell Anemia: A Prospective Evaluation of Polyoma (BK) Virus Infection and Treatment with Cidofovir

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