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Abdullah Al Jefri
Observed names:
A. Al Jefri,
Abdullah Al-Jefri
Institution:
King Faisal Specialist Hospital & Research Centre
Observed institution:
King Faisal Specialist Hospital & Research Centre
OpenAlex ID:
A5072408243
Second Allogeneic Bone Marrow Transplantation after Myeloablative Conditioning Analysis of 43 Cases from Single Institution
2004
·
A. Al Shanqeeti
, P. Seth
, et al.
·
Hematology
·
26
PDF
Hematopoietic Stem Cell Transplantation in the Eastern Mediterranean Region (EMRO) 2008-2009: Report on behalf of the Eastern Mediterranean Bone Marrow Transplantation (EMBMT) Group
2011
·
Said Yousef Ahmed Mohamed
, Ibtihal Fadhil
, et al.
·
Hematology/Oncology and Stem Cell Therapy
·
17
PDF
Cytomegalovirus infections in unrelated cord blood transplantation in pediatric patients: incidence, risk factors, and outcomes
2011
·
Sami Al Hajjar
, Amal Al Seraihi
, et al.
·
Hematology/Oncology and Stem Cell Therapy
·
13
Multicenter Validation of Spin-Density Projection-Assisted R2-MRI for the Non-Invasive Measurement of Liver Iron Concentration
2010
·
Timothy G St Pierre
, Amal El-Beshlawy
, et al.
·
Blood
·
5
Deferasirox (Exjade®) Treatment in Pediatric β-Thalassemia Patients with High Iron Burden: 2.8 Years Results from ESCALATOR Trial
2008
·
Ali Taher
, Abdullah Al Jefri
, et al.
·
Blood
·
3
Efficacy and Safety of Once-Daily Oral Deferasirox (Exjade®) during a Median of 2.7 Years of Treatment in Heavily Iron-Overloaded Patients with β-Thalassemia
2008
·
Ali Taher
, Amal El-Beshlawy
, et al.
·
Blood
·
3
Oral Deferasirox (Exjade®, ICL670) Is Effective, with a Clinically Manageable Safety Profile, in Pediatric β-Thalassemia Patients with High Iron Burden.
2007
·
Ali Taher
, Abdullah Al Jefri
, et al.
·
Blood
·
3
Noval Mutation in Four Saudi Families with Glanzmann Thrombasthenia
2011
·
Tarek Owaidah
, Hala Abalkhail
, et al.
·
Blood
·
2
Deferasirox (Exjade®, ICL670) Treatment of Inadequately Chelated β-Thalassemia Patients from the Middle East: The ESCALATOR Trial.
2005
·
Ali Taher
, Amal El-Beshlawy
, et al.
·
Blood
·
2
Deferasirox (Exjade®, ICL670) Is Effective and Tolerable in β-Thalassemia Patients with High Iron Burden and History of Inadequate Chelation Therapy.
2006
·
A. Taher
, A. El-Beshlawy
, et al.
·
Blood
·
1
Allogeneic Stem Cell Transplantation (sct) for Patients (pts) With Thalassemia Major: the Asian Experiences
2006
·
Abdullah Al Jefri
, Mohamad Fekredeen Ayas
, et al.
·
1
Pediatric Acute Myeloid Leukemia with KMT2A rearrangement -- can Partner Gene Help Determine Need for Hematopoietic Stem Cell Transplant?
2020
·
Ibrahim Al Ghemlas
, Saadiya Khan
, et al.
PDF
Contents Vol. 123, 2010
2010
·
Reinhold Munker
, Chang-Gong Liu
, et al.
·
Acta Haematologica
PDF
Author Index Vol. 123, 2010
2010
·
Reinhold Munker
, Chang-Gong Liu
, et al.
·
Acta Haematologica
PDF
Danurubicin, cytosine arabinoside, etoposide, dexamethasone versus idarubicin, cytosine arabinoside, thioguanine in the treatment of childhood acute myeloid leukemia
1999
·
Samira Rifai
, M. M. Mustafa
, et al.
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Works count:
15
Citation count:
76
H-index:
4
I10-index:
3
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