Bone marrow embolism in sickle cell disease: A review
β Scribed by Nghia C. Dang; Cage Johnson; Mahmoud Eslami-Farsani; L. Julian Haywood
- Publisher
- John Wiley and Sons
- Year
- 2005
- Tongue
- English
- Weight
- 91 KB
- Volume
- 79
- Category
- Article
- ISSN
- 0361-8609
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## Abstract Sickle cell anemia (SCA) is an inherited disorder of hemoglobin synthesis that is characterized by lifeβlong severe hemolytic anemia, attacks of pain crisis, and chronic organ system damage. A third of the hemolysis in SCA is intravascular and the resulting urinary losses of iron may le
Antiphospholipid antibody formation can be Induced In mice by phospholipid In a hexagonal II phase but not by phospholipid in a bllayer phase. Since sickle red cell membranes have increased hexagonal I1 phase content, we have measured serum antiphospholipid antibody levels in 25 patients with sickle