A. Al-Suliman

发表

Demands and challenges for patients with sickle‐cell disease requiring hematopoietic stem cell transplantation in Saudi Arabia

W. Jastaniah, A. Alsultan, M. Alabdulaali, 2016, Pediatric transplantation.

Management of adult immune thrombocytopenia: Recommendations by an expert Saudi panel

A. Aleem, H. Al-Hashmi, H. Al-Zahrani, 2019, Journal of Applied Hematology.

Co-inheritance of novel ATRX gene mutation and globin (α & β) gene mutations in transfusion dependent beta-thalassemia patients.

M. Steinberg, J. Borgio, S. Abdulazeez, 2015, Blood cells, molecules & diseases.

Fetal hemoglobin in sickle cell anemia: genetic studies of the Arab-Indian haplotype.

P. Sebastiani, L. Farrer, C. Baldwin, 2013, Blood cells, molecules & diseases.

KLF1 gene and borderline hemoglobin A2 in Saudi population

J. Borgio, S. Abdulazeez, A. Al-Ali, 2017, Archives of medical science : AMS.

Co-inheritance of alpha globin gene deletion lowering serum iron level in female beta thalassemia patients

J. Borgio, N. B. Almandil, S. Abdulazeez, 2019, Molecular Biology Reports.

Utilizing Whole-Exome Sequencing to Characterize the Phenotypic Variability of Sickle Cell Disease.

A. Alsultan, M. Alfadhel, A. Aleem, 2018, Genetic testing and molecular biomarkers.

deletion in α ‐ globin genes increases the concentration of fetal hemoglobin and hemoglobin A 2 in a Saudi Arabian population

H. Qutub, J. Borgio, S. Abdulazeez, 2017 .

Mutations in the β‐globin gene from a Saudi population: an update

M. Steinberg, J. Borgio, S. Abdulazeez, 2016, International journal of laboratory hematology.

BCL11A enhancer haplotypes and fetal hemoglobin in sickle cell anemia.

P. Sebastiani, L. Farrer, V. Vathipadiekal, 2015, Blood cells, molecules & diseases.