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Journal Articles

Outcome of Hematopoietic Stem Cell Transplantation in Children with Primary Hemophagocytic Lymphohistiocytosis: A Single Institution Experience Using Reduced Intensity Conditioning

Mohammed Essa, Enas Basher, Rodaina Abujoub, Abdulrahman Alsultan, MD

Blood (2020) 136 (Supplement 1): 43–44.

https://doi.org/10.1182/blood-2020-142988

Published: 2020

Journal Articles

The Current Practice of Management of Asymptomatic Central Venous Catheters Associated Venous Thromboembolism in Children: A Result of Saudi Arabian Pediatric Hematology/Oncology Society Survey

Bader Allahyani, MD, Abdullah Ali, MD, Joshua Feder, MD, Mohammad Alshahrani, MD, Abdulrahman Alsultan, MD, Azzah Alzahrani, MD

Blood (2020) 136 (Supplement 1): 3–4.

https://doi.org/10.1182/blood-2020-133813

Published: 2020

Journal Articles

A Library of Sickle Cell Anemia Induced Pluripotent Stem Cells of Diverse Haplotypes and Ethnicities

Seonmi Park, Andreia Gianotti-Sommer, David H.K. Chui, MD, Maria Stella Figueiredo, MDPhD, Abdulrahman Alsultan, MD, Amein Al-Ali, Martin H Steinberg, Professor, of, MDcine, George J. Murphy, PhD, Gustavo Mostoslavsky

Blood (2015) 126 (23): 2354.

https://doi.org/10.1182/blood.V126.23.2354.2354

Published: 2015

Journal Articles

Polymorphisms Associated with the Arab-Indian Haplotype of Sickle Cell Anemia Are Candidate Fetal Hemoglobin Gene Modulators

Vinod Vathipadiekal, PhD, Abdulrahman Alsultan, MD, John Farrell, PhD, A.M Al-Rubaish, Fahad Al-Muhanna, Z Naserullah, A Alsuliman, P.K. Patra, Jacqueline Milton, Lindsay Farrer, David H.K. Chui, MD, Amein Al-Ali, Paola Sebastiani, PhD, Martin H. Steinberg, MD

Blood (2015) 126 (23): 3388.

https://doi.org/10.1182/blood.V126.23.3388.3388

Published: 2015

Journal Articles

A Candidate Trans-Acting Modulator of Fetal Hemoglobin Gene Expression in the Arab-Indian Haplotype of Sickle Cell Anemia

Blood (2015) 126 (23): 409.

https://doi.org/10.1182/blood.V126.23.409.409

Published: 2015

Journal Articles

BCL11A enhancer Haplotypes Are Associated with the Distribution of HbF in Arab-Indian and African Haplotype Sickle Cell Anemia but Not the Different Population Levels of HbF

Paola Sebastiani, PhD, John J. Farrell, PhD, Shuai Wang, MS, Heather L Edward, BA, Heather M. Shappell, BS, Harold T. Bae, PhD, Clinton T. Baldwin, PhD, A. M. Al-Rubaish, MD, Zaki Naserullah, MD, Ahmed Alsuliman, MD, Pradeep K. Patra, PhD, Lindsay A. Farrer, PhD, David H.K. Chui, MD, Abdulrahman Alsultan, MD, Duyen A. Ngo, MD, Haifa Kathrin Al-Ali, MD, Martin H. Steinberg, MD

Blood (2014) 124 (21): 4066.

https://doi.org/10.1182/blood.V124.21.4066.4066

Published: 2014

Journal Articles

Fetal Hemoglobin In Sickle Cell Anemia: A Glass Half Full?

Martin H. Steinberg, MD, David H.K. Chui, MD, George J. Dover, MD, Paola Sebastiani, PhD, Abdulrahman Alsultan, MD

Blood (2013) 122 (21): 4691.

https://doi.org/10.1182/blood.V122.21.4691.4691

Published: 2013

Journal Articles

Successful Engraftment In Children With Severe Aplastic Anemia After Transplantation Of HLA-Identical Hematopoietic Donor Cells With Shorter Telomere Length

Abdulrahman Alsultan, MD, Gabriela M. Baerlocher, MD, Elisabeth Oppliger Leibundgut, PharmD, Sameera AlAfghani, MD, Reem Al-Sudairy, MD, Mohammed Al Balwi, PhD, Mohammed Jarrar, MD

Blood (2013) 122 (21): 2047.

https://doi.org/10.1182/blood.V122.21.2047.2047

Published: 2013

Journal Articles

Activation-Resistant Homozygous Protein C R229W Mutation Causing Familial Perinatal Intracranial Hemorrhage

Abdulrahman Alsultan, MD, Andrew J. Gale, PhD, Kadijah Kurban, MD, Mohammed Khalifah, MD, Fahad B. Albadr, MD, John H. Griffin, PhD

Blood (2013) 122 (21): 3587.

https://doi.org/10.1182/blood.V122.21.3587.3587

Published: 2013

Journal Articles

Induced Pluripotent Stem Cell Modeling of Sickle Cell Anemia

Sarah S Rozelle, Brenden W Smith, Efthymia Melista, Ehimen Aneni, MD, Paola Sebastiani, PhD, Clinton T. Baldwin, PhD, Abdulrahman Alsultan, MD, David H.K. Chui, MD, Gustavo Mostoslavsky, M.D., Ph.D, Martin H. Steinberg, MD, George J. Murphy, Ph.D

Blood (2012) 120 (21): 3233.

https://doi.org/10.1182/blood.V120.21.3233.3233

Published: 2012

Journal Articles

Co-Inheritance of Delta Thalassemia Might Contribute to the High Fetal Hemoglobin in Sickle Cell Anemia Patients with the Saudi-Indian Haplotype

Abdulrahman Alsultan, MD, Duyen A. Ngo, MD, John J. Farrell, MS, Hazem Ghabbour, Idowu Akinsheye, PhD, Amein Al-Ali, PhD, Ahmed Alsuliman, MD, Muneer Al-Baghshi, MD, Waleed Albuali, MD, Mohammed Alabdulaali, MD, Paola Sebastiani, PhD, Clinton T. Baldwin, PhD, David H.K. Chui, MD, Martin H. Steinberg, MD

Blood (2011) 118 (21): 1056.

https://doi.org/10.1182/blood.V118.21.1056.1056

Published: 2011

Journal Articles

Fetal Hemoglobin In Sickle Cell Anemia: Molecular Characterization of Saudi Patients From the Southwestern Province.

Abdulrahman Alsultan, MD, Nadia Solovieff, Aamer Aleem, MBBS, Farjah H. AlGahtani, MBBS, Ali Al-Shehri, MBBS, Mohamed Elfaki Osman, MBBS, Kadijah Kurban, MBBS, Hasan Bahakim, MD, Abdul Kareem Al-Momen, MBBS, FRCPC, David H.K. Chui, MD, Martin H. Steinberg, MD

Blood (2010) 116 (21): 1621.

https://doi.org/10.1182/blood.V116.21.1621.1621

Published: 2010

Journal Articles

Fetal Hemoglobin In Sickle Cell Anemia: Molecular Characterization of Saudi Patients From the Eastern Province

Abdulrahman Alsultan, MD, Idowu Akinsheye, Nadia Solovieff, Hazem Ghabbour, Duyen A. Ngo, MD, Daniel A Dworkis, Clinton T. Baldwin, PhD, Paola Sebastiani, PhD, Lindsay A. Farrer, PhD, Martin H. Steinberg, MD, David H.K. Chui, MD

Blood (2010) 116 (21): 1627.

https://doi.org/10.1182/blood.V116.21.1627.1627

Published: 2010

NARROW

Outcome of Hematopoietic Stem Cell Transplantation in Children with Primary Hemophagocytic Lymphohistiocytosis: A Single Institution Experience Using Reduced Intensity Conditioning

The Current Practice of Management of Asymptomatic Central Venous Catheters Associated Venous Thromboembolism in Children: A Result of Saudi Arabian Pediatric Hematology/Oncology Society Survey

A Library of Sickle Cell Anemia Induced Pluripotent Stem Cells of Diverse Haplotypes and Ethnicities

Polymorphisms Associated with the Arab-Indian Haplotype of Sickle Cell Anemia Are Candidate Fetal Hemoglobin Gene Modulators

A Candidate Trans-Acting Modulator of Fetal Hemoglobin Gene Expression in the Arab-Indian Haplotype of Sickle Cell Anemia

BCL11A enhancer Haplotypes Are Associated with the Distribution of HbF in Arab-Indian and African Haplotype Sickle Cell Anemia but Not the Different Population Levels of HbF

Fetal Hemoglobin In Sickle Cell Anemia: A Glass Half Full?

Successful Engraftment In Children With Severe Aplastic Anemia After Transplantation Of HLA-Identical Hematopoietic Donor Cells With Shorter Telomere Length

Activation-Resistant Homozygous Protein C R229W Mutation Causing Familial Perinatal Intracranial Hemorrhage

Induced Pluripotent Stem Cell Modeling of Sickle Cell Anemia

Co-Inheritance of Delta Thalassemia Might Contribute to the High Fetal Hemoglobin in Sickle Cell Anemia Patients with the Saudi-Indian Haplotype

Fetal Hemoglobin In Sickle Cell Anemia: Molecular Characterization of Saudi Patients From the Southwestern Province.

Fetal Hemoglobin In Sickle Cell Anemia: Molecular Characterization of Saudi Patients From the Eastern Province

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American Society of Hematology

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American Society of Hematology

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