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Title
Sickle cell disease and stroke
Authors
Keywords
-
Journal
BLOOD
Volume 114, Issue 25, Pages 5117-5125
Publisher
American Society of Hematology
Online
2009-10-02
DOI
10.1182/blood-2009-05-220921
References
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Related references
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- Hydroxyurea for the Treatment of Sickle Cell Anemia
- (2008) Orah S. Platt NEW ENGLAND JOURNAL OF MEDICINE
- A critical assessment of transcranial doppler screening rates in a large pediatric sickle cell center: Opportunities to improve healthcare quality
- (2008) Jean L. Raphael et al. PEDIATRIC BLOOD & CANCER
- Genome-wide association study shows BCL11A associated with persistent fetal hemoglobin and amelioration of the phenotype of -thalassemia
- (2008) M. Uda et al. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
- DNA polymorphisms at the BCL11A, HBS1L-MYB, and -globin loci associate with fetal hemoglobin levels and pain crises in sickle cell disease
- (2008) G. Lettre et al. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
- Human Fetal Hemoglobin Expression Is Regulated by the Developmental Stage-Specific RepressorBCL11A
- (2008) Vijay G. Sankaran et al. SCIENCE
- The role of natural killer T cells in lung inflammation
- (2007) R Boyton JOURNAL OF PATHOLOGY
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