Sickle cell disease in the Eastern Province of Saudi Arabia: Clinical and laboratory features-Reference-Cited by-同舟云学术

Sickle cell disease in the Eastern Province of Saudi Arabia: Clinical and laboratory features

Published:2021-01-28 Issue:4 Volume:96 Page:
ISSN:0361-8609
Container-title:American Journal of Hematology
language:en
Short-container-title:Am J Hematol

Author:

Al‐Ali Amein K.¹²,Alsulaiman Ahmed¹³,Alfarhan Mohammed¹⁴,Safaya Surinder¹^ORCID,Vatte Chitti Babu²,Albuali Waleed M.¹,Qutub Hatem O.¹,Alzahrani Alhusain J.⁵,Milton Jacqueline N.⁶,Steinberg Martin H.⁷^ORCID

Affiliation:

1. Alomran Scientific Chair, King Faisal University Al‐Ahsa Saudi Arabia

2. Department of Clinical Biochemistry College of Medicine, Imam Abdulrahman bin Faisal University Dammam Saudi Arabia

3. Department of Internal Medicine King Fahd Hospital Al‐Ahsa Saudi Arabia

4. Department of Orthopedic Surgery College of Medicine, King Faisal University Al‐Ahsa Saudi Arabia

5. Department of Applied Medical Sciences University of Hafre Al Batin Saudi Arabia

6. Department of Statistics Boston University School of Public Health Boston Massachusetts

7. Department of Medicine, Center of Excellence in Sickle Cell Disease Boston University and Boston Medical Center Boston Massachusetts

Publisher

Wiley

Subject

Hematology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/ajh.26096

Reference10 articles.

1. Two different forms of homozygous sickle cell disease occur in Saudi Arabia

2. Fetal hemoglobin in sickle cell anemia

3. Sickle cell disease in Saudi Arabia: the phenotype in adults with the Arab-Indian haplotype is not benign

4. Prevalence and Diversity of Haplotypes of Sickle Cell Disease in the Eastern Province of Saudi Arabia

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

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