Regional Variations in Sickle Cell Anemia in Saudi Arabia
Author:
Affiliation:
1. From the Department of Pathology and Laboratory Medicine, King Faisal Specialist Hospital and Research Centre, Riyadh
2. From the Department of Oncology, King Faisal Specialist Hospital and Research Centre, Riyadh
Publisher
King Faisal Specialist Hospital and Research Centre
Subject
General Medicine
Reference25 articles.
1. Benign sickle-cell anemia;Perrine RP;Lancet,1972
2. Natural history of sickle cell anemia in Saudi Arabs: a study of 270 subjects;Perrine RP;Ann Intern Med,1978
3. Delay time of gelation: possible determinant of clinical severity in sickle cell disease (editorial);Eaton WA;Blood,1976
4. Effect of alpha thalassaemia on the rheology of homozygous sickle cell disease;Serjeant BE;Br J Haematol,1983
5. Haemoglobin Bart's in Saudi Arabia;Pembrey ME;Br J Haematol,1975
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1. Sickle cell morbidity profile in Omani children;Annals of Tropical Paediatrics;2002-03
2. Sickle Cell Disease: Patients' Awareness and Management;Annals of Saudi Medicine;1998-01
3. Sickle Cell Gene in the Population of Saudi Arabia;Hemoglobin;1996-01
4. Acute phase reactants and severity of homozygous sickle cell disease;Journal of Internal Medicine;1993-06
5. Serum immunoglobulin (G, A and M) classes and IgG subclasses in sickle cell anaemia;APMIS;1993-01
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