Publications by authors named "Abdullah Al Jefri"

28Publications

Successful Outcome in Patients with Fanconi Anemia Undergoing T Cell-Replete Mismatched Related Donor Hematopoietic Cell Transplantation Using Reduced-Dose Cyclophosphamide Post-Transplantation.

Biol Blood Marrow Transplant 2019 11 12;25(11):2217-2221. Epub 2019 Jul 12.

Department of Pediatric Hematology/Oncology, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia.

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http://dx.doi.org/10.1016/j.bbmt.2019.07.010DOI Listing
November 2019

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.

J Pediatr Hematol Oncol 2017 01;39(1):33-37

*Department of Pediatric Hematology/Oncology, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia †Jordan University of Science & Technology, Irbid, Jordan.

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http://dx.doi.org/10.1097/MPH.0000000000000679DOI Listing
January 2017

Factors affecting the outcome of related allogeneic hematopoietic cell transplantation in patients with Fanconi Anemia.

Biol Blood Marrow Transplant 2014 Oct 21;20(10):1599-603. Epub 2014 Jun 21.

Department of Pediatric Hematology Oncology, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia.

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http://dx.doi.org/10.1016/j.bbmt.2014.06.016DOI Listing
October 2014

Outcome of allogeneic stem cell transplantation with a conditioning regimen of busulfan, cyclophosphamide and low-dose etoposide for children with myelodysplastic syndrome.

Hematol Oncol Stem Cell Ther 2011 ;4(3):121-5

Department of Pediatrics, King Faisal Specialist Hospital and Research Centre, Riyadh, Saudi Arabia.

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http://dx.doi.org/10.5144/1658-3876.2011.121DOI Listing
February 2012

Advances in allogeneic stem cell transplantation for hemoglobinopathies.

Hemoglobin 2011 3;35(5-6):469-75. Epub 2011 Oct 3.

Department of Pediatric Hematology and Oncology, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia.

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http://dx.doi.org/10.3109/03630269.2011.618567DOI Listing
March 2012

The Saudi experience in fludarabine-based conditioning regimens in patients with Fanconi anemia undergoing stem cell transplantation: excellent outcome in recipients of matched related stem cells but not in recipients of unrelated cord blood stem cells.

Biol Blood Marrow Transplant 2012 Apr 24;18(4):627-32. Epub 2011 Aug 24.

Section of Pediatric Stem Cell Transplantation, Department of Pediatric Hematology-Oncology, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia.

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http://dx.doi.org/10.1016/j.bbmt.2011.08.015DOI Listing
April 2012

Cytomegalovirus infections in unrelated cord blood transplantation in pediatric patients: incidence, risk factors, and outcomes.

Hematol Oncol Stem Cell Ther 2011 ;4(2):67-72

Department of Pediatric, King Faisal Specialist Hospital and Research Centre, Riyadh, Saudi Arabia.

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http://dx.doi.org/10.5144/1658-3876.2011.67DOI Listing
December 2011

Allogeneic hematopoietic stem cell transplantation in leukocyte adhesion deficiency type 1: a single center experience.

Biol Blood Marrow Transplant 2011 Aug 8;17(8):1245-9. Epub 2011 Jan 8.

Section of Pediatric Allergy/Immunology, Department of Pediatrics, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia.

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http://dx.doi.org/10.1016/j.bbmt.2010.12.714DOI Listing
August 2011

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

Pediatr Blood Cancer 2011 Feb 22;56(2):289-93. Epub 2010 Oct 22.

Section of Pediatric Stem Cell Transplantation, Department of Pediatric Hematology-Oncology, King Faisal Specialist Hospital & Research Center, Riyadh, Saudi Arabia.

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http://dx.doi.org/10.1002/pbc.22804DOI Listing
February 2011

A novel HAX1 gene mutation in severe congenital neutropenia (SCN) associated with neurological manifestations.

Eur J Pediatr 2010 Jun 25;169(6):661-6. Epub 2010 Feb 25.

Department of Pathology and Laboratory Medicine, Molecular Genetics Laboratory, King Faisal Specialist Hospital & Research Centre, PO Box 3354, MBC#10, Riyadh 11211, Saudi Arabia.

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http://dx.doi.org/10.1007/s00431-010-1150-6DOI Listing
June 2010

Allogeneic stem cell transplantation using myeloablative and reduced-intensity conditioning in patients with major histocompatibility complex class II deficiency.

Biol Blood Marrow Transplant 2010 Jun 14;16(6):818-23. Epub 2010 Jan 14.

Section of Pediatric Allergy and Immunology, Department of Pediatrics, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia.

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http://dx.doi.org/10.1016/j.bbmt.2010.01.002DOI Listing
June 2010

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

Eur J Haematol 2009 Jun 28;82(6):458-65. Epub 2009 Jan 28.

Department of Internal Medicine, Hematology, Oncology Division, American University of Beirut Medical Center, Beirut, Lebanon.

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http://dx.doi.org/10.1111/j.1600-0609.2009.01228.xDOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2730551PMC
June 2009

Second stem cell transplantation in patients with Fanconi anemia using antithymocyte globulin alone for conditioning.

Biol Blood Marrow Transplant 2008 Apr;14(4):445-8

Section of Pediatric Stem Cell Transplant, Department of Pediatric Hematology-Oncology, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia.

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http://dx.doi.org/10.1016/j.bbmt.2008.02.004DOI Listing
April 2008

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.

Pediatr Blood Cancer 2006 Dec;47(7):926-30

Department of Pediatric Hematology-Oncology, Section of Stem Cell Transplant, KFSHRC, Riyadh, Saudi Arabia.

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http://dx.doi.org/10.1002/pbc.20758DOI Listing
December 2006

Intra-leukocytic hemosiderin inclusions detected as pseudoeosinophils by automated depolarization analysis in a patient with beta-thalassaemia major and immune hemolysis.

Blood Cells Mol Dis 2005 Mar-Apr;34(2):162-5

Department of Pathology and Laboratory Medicine, King Faisal Specialist Hospital and Research Centre, Riyadh, Saudi Arabia.

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http://linkinghub.elsevier.com/retrieve/pii/S107997960500003
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http://dx.doi.org/10.1016/j.bcmd.2004.12.005DOI Listing
September 2005

Does adding ATG to the GVHD prophylaxis regimen help reduce its incidence?

Bone Marrow Transplant 2003 Feb;31(4):311; author reply 313

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http://dx.doi.org/10.1038/sj.bmt.1703804DOI Listing
February 2003