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Multicenter validation of spin-density projection-assisted R2-MRI for the noninvasive measurement of liver iron concentration

Magnetic resonance in medicine, 2014-06, Vol.71 (6), p.2215-2223

2014

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Chimerism Analysis of Cell-Free DNA in Patients Treated with Hematopoietic Stem Cell Transplantation May Predict Early Relapse in Patients with Hematologic Malignancies

Biotechnology Research International, 2016-01, Vol.2016, p.8589270-6

2016

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Advances in Allogeneic Stem Cell Transplantation for Hemoglobinopathies

Hemoglobin, 2011-10, Vol.35 (5-6), p.469-475

Al Jefri, Abdullah H.

2011

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In cyclosporine induced neurotoxicity, is tacrolimus an appropriate substitute or is it out of the frying pan and into the fire?

Pediatric Blood & Cancer, 2008-02, Vol.50 (2), p.426-426

2008

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Dexamethasone‐associated toxicity during induction chemotherapy for childhood acute lymphoblastic leukemia is augmented by concurrent use of daunomycin

Cancer, 2003-06, Vol.97 (11), p.2898-2903

2003

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Outcome of second allogenic stem cell transplantation in pediatric patients with non-malignant hematological and immune deficiency disorders

Pediatric blood & cancer, 2011-02, Vol.56 (2), p.289-293

2011

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The outcome of children with acute myeloid leukemia (AML) post-allogeneic stem cell transplantation (SCT) is not improved by the addition of etoposide to the conditioning regimen

Pediatric Blood & Cancer, 2006-12, Vol.47 (7), p.926-930

2006

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Hematopoietic stem cell transplantation in patients with Fanconi anemia: a report of late effects and psychosocial adjustment in life

Bone marrow transplantation (Basingstoke), 2024-01, Vol.59 (1), p.141-143

2024

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Congenital sideroblastic anaemia successfully treated using allogeneic stem cell transplantation

British journal of haematology, 2001-06, Vol.113 (4), p.938-939

2001

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Distinct mutations in STXBP2 are associated with variable clinical presentations in patients with familial hemophagocytic lymphohistiocytosis type 5 (FHL5)

Blood, 2012-06, Vol.119 (25), p.6016-6024

2012

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Impact of Race on Gvhd after Unrelated Cord Blood Transplantation: Comparison of Outcome in National and International Cord Blood Units' Recipients

Biology of blood and marrow transplantation, 2016-03, Vol.22 (3), p.S388-S388

2016

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Outcome of Unmanipulated HLA-Mismatched/Haplo-Matched Hematopoietic Cell Transplantation from Related Donors in Patients with Fanconi Anemia Using Low Dose Post HCT Cyclophosphamide for Gvhd Prophylaxis

Biology of blood and marrow transplantation, 2016-03, Vol.22 (3), p.S366-S366

2016

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HLA-haploidentical donor transplants with post-transplant cyclophosphamide in children with primary immune deficiency disorders

Bone marrow transplantation (Basingstoke), 2022-04, Vol.57 (4), p.668-670

2022

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Essential Thrombocythemia in Children: A Retrospective Study

Journal of hematology, 2021-06, Vol.10 (3), p.106-113

2021

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Hematopoietic Stem Cell Transplantation Stabilizes Cerebral Vasculopathy in High-Risk Pediatric Sickle Cell Disease Patients: Evidence From a Referral Transplant Center

Journal of hematology, 2022-02, Vol.11 (1), p.8-14

2022

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Efficacy and safety of deferasirox, an oral iron chelator, in heavily iron-overloaded patients with β-thalassaemia: the ESCALATOR study

European journal of haematology, 2009-06, Vol.82 (6), p.458-465

2009

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Clofarabine in Pediatric Acute Relapsed or Refractory Leukemia: Where Do We Stand on the Bridge to Hematopoietic Stem Cell Transplantation?

Journal of hematology, 2023-02, Vol.12 (1), p.16-26

2023

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Factors Determining the Outcome of Hematopoietic Stem Cell Transplantation in Patients With Acute Lymphoblastic Leukemia at King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia

Journal of pediatric hematology/oncology, 2017-01, Vol.39 (1), p.33-37

2017

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Does Mixed Chimerism After Allogeneic Hematopoietic Cell Transplantation in Pediatric Patients With Fanconi Anemia Impact on Outcome?

Transplantation and cellular therapy, 2021-03, Vol.27 (3), p.257.e1-257.e6

2021

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Graft Versus Host Disease Following HLA-Matched Sibling Donor Compared with Matched Related Donor for Hematopoietic Stem Cell Transplantation for the Treatment of Severe Combined Immunodeficiency Disease

Journal of clinical immunology, 2019-05, Vol.39 (4), p.414-420

2019

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Erythrocytosis Post Allogeneic Stem Cell Transplantation, An Observational Study Of Hemoglobin Levels On Long-Term Follow Up Post Transplantation In Patients With Fanconi Or Acquired Aplastic Anemia

Blood, 2013-11, Vol.122 (21), p.4643-4643

2013

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HEMOPHAGOCYTOSIS COMPLICATING KAWASAKI DISEASE

Pediatric hematology and oncology, 2000-06, Vol.17 (4), p.323-329

2000

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Importance of optimal dosing ≥30 mg/kg/d during deferasirox treatment: 2.7-yr follow-up from the ESCALATOR study in patients with β-thalassaemia

European journal of haematology, 2011-10, Vol.87 (4), p.355-365

2011

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Factors Affecting Outcome of Related Allogeneic Hematopoietic Cell Transplantation in Patients with Fanconi Anemia

Blood, 2012-11, Vol.120 (21), p.3100-3100

2012

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Multicenter validation of spin-density projection-assisted R2-MRI for the noninvasive measurement of liver iron concentration

Allogeneic Hematopoietic Cell Transplantation for Fanconi Anemia in Patients With Pretransplantation Cytogenetic Abnormalities, Myelodysplastic Syndrome, or Acute Leukemia

Chimerism Analysis of Cell-Free DNA in Patients Treated with Hematopoietic Stem Cell Transplantation May Predict Early Relapse in Patients with Hematologic Malignancies

Advances in Allogeneic Stem Cell Transplantation for Hemoglobinopathies

In cyclosporine induced neurotoxicity, is tacrolimus an appropriate substitute or is it out of the frying pan and into the fire?

Dexamethasone‐associated toxicity during induction chemotherapy for childhood acute lymphoblastic leukemia is augmented by concurrent use of daunomycin

Outcome of second allogenic stem cell transplantation in pediatric patients with non-malignant hematological and immune deficiency disorders

The outcome of children with acute myeloid leukemia (AML) post-allogeneic stem cell transplantation (SCT) is not improved by the addition of etoposide to the conditioning regimen

Hematopoietic stem cell transplantation in patients with Fanconi anemia: a report of late effects and psychosocial adjustment in life

Congenital sideroblastic anaemia successfully treated using allogeneic stem cell transplantation

Distinct mutations in STXBP2 are associated with variable clinical presentations in patients with familial hemophagocytic lymphohistiocytosis type 5 (FHL5)

Impact of Race on Gvhd after Unrelated Cord Blood Transplantation: Comparison of Outcome in National and International Cord Blood Units' Recipients

Outcome of Unmanipulated HLA-Mismatched/Haplo-Matched Hematopoietic Cell Transplantation from Related Donors in Patients with Fanconi Anemia Using Low Dose Post HCT Cyclophosphamide for Gvhd Prophylaxis

HLA-haploidentical donor transplants with post-transplant cyclophosphamide in children with primary immune deficiency disorders

Essential Thrombocythemia in Children: A Retrospective Study

Hematopoietic Stem Cell Transplantation Stabilizes Cerebral Vasculopathy in High-Risk Pediatric Sickle Cell Disease Patients: Evidence From a Referral Transplant Center

Efficacy and safety of deferasirox, an oral iron chelator, in heavily iron-overloaded patients with β-thalassaemia: the ESCALATOR study

Clofarabine in Pediatric Acute Relapsed or Refractory Leukemia: Where Do We Stand on the Bridge to Hematopoietic Stem Cell Transplantation?

Factors Determining the Outcome of Hematopoietic Stem Cell Transplantation in Patients With Acute Lymphoblastic Leukemia at King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia

Does Mixed Chimerism After Allogeneic Hematopoietic Cell Transplantation in Pediatric Patients With Fanconi Anemia Impact on Outcome?

Graft Versus Host Disease Following HLA-Matched Sibling Donor Compared with Matched Related Donor for Hematopoietic Stem Cell Transplantation for the Treatment of Severe Combined Immunodeficiency Disease

Erythrocytosis Post Allogeneic Stem Cell Transplantation, An Observational Study Of Hemoglobin Levels On Long-Term Follow Up Post Transplantation In Patients With Fanconi Or Acquired Aplastic Anemia

HEMOPHAGOCYTOSIS COMPLICATING KAWASAKI DISEASE

Importance of optimal dosing ≥30 mg/kg/d during deferasirox treatment: 2.7-yr follow-up from the ESCALATOR study in patients with β-thalassaemia

Factors Affecting Outcome of Related Allogeneic Hematopoietic Cell Transplantation in Patients with Fanconi Anemia

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