Skip to search formSkip to main contentSkip to account menu

Anemia, Sickle Cell

Known as: Cell Diseases, Sickle, Cell Disorders, Sickle, Hemoglobin SS Disease 
An inherited disease in which the red blood cells have an abnormal crescent shape, block small blood vessels, and do not last as long as normal red… 
National Institutes of Health

Related topics

Related topics

41 relations
0.5 ML Alprostadil 0.02 MG/ML Prefilled SyringeAbdominal PainAcute Chest SyndromeAlprostadil

Broader (6)

AnemiaAnemia, HemolyticAnemia, Hemolytic, CongenitalHematological Disease

Narrower (2)

Hemoglobin SC DiseaseHemoglobin SS disease with crisis

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
Highly Cited
2006
Highly Cited
2006
Stroke Prevention Trial in Sickle Cell Anemia (STOP): extended follow-up and final results.
The Stroke Prevention Trial in Sickle Cell Anemia (STOP) was a randomized trial to evaluate whether chronic transfusion could… 
Review
2005
Review
2005
Control of globin gene expression during development and erythroid differentiation.
Highly Cited
2003
Highly Cited
2003
Sickle blood contains tissue factor-positive microparticles derived from endothelial cells and monocytes.
Blood microparticles (MPs) in sickle cell disease (SCD) are reportedly derived only from erythrocytes and platelets. Yet in SCD… 
Highly Cited
2001
Highly Cited
2001
Silent infarction as a risk factor for overt stroke in children with sickle cell anemia: a report from the Cooperative Study of Sickle Cell Disease.
OBJECTIVE To determine whether children with homozygous sickle cell anemia (SCD) who have silent infarcts on magnetic resonance… 
Highly Cited
2000
Highly Cited
2000
Multicenter Prospective Study of Children With Sickle Cell Disease: Radiographic and Psychometric Correlation
After obtaining familial informed consent, between January 1996 and July 1997, 173 children (5 to 15 years old) with sickle cell… 
Highly Cited
1996
Highly Cited
1996
Increased erythrocyte phosphatidylserine exposure in sickle cell disease: flow-cytometric measurement and clinical associations.
Increased exposure of phosphatidylserine (PS) in erythrocytes has been postulated to contribute to the pathophysiology of sickle… 
Review
1990
Review
1990
Sickle cell hemoglobin polymerization.
Highly Cited
1984
Highly Cited
1984
Hydroxyurea enhances fetal hemoglobin production in sickle cell anemia.
Hydroxyurea, a widely used cytotoxic/cytostatic agent that does not influence methylation of DNA bases, increases fetal… 
Highly Cited
1984
Highly Cited
1984
Bone-marrow transplantation in a patient with sickle-cell anemia.
SICKLE-CELL anemia affects 1 in 600 of the U.S. black population and accounts for 80,000 deaths annually throughout the world.1… 
Highly Cited
1983
Highly Cited
1983
Erythrocytes in sickle cell anemia are heterogeneous in their rheological and hemodynamic characteristics.
To understand the contribution to the pathophysiology of sickle cell anemia of the different erythrocyte density types present in… 
By clicking accept or continuing to use the site, you agree to the terms outlined in our Privacy Policy (opens in a new tab), Terms of Service (opens in a new tab), and Dataset License (opens in a new tab)