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hemoglobin AA

Known as: HbAA, haemoglobin AA, hemoglobin AA (HbAA) 
 
National Institutes of Health

Papers overview

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Highly Cited
2015
Highly Cited
2015
Abstract Chronic pain is a major characteristic feature of sickle cell disease (SCD). The refractory nature of pain and the… Expand
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Highly Cited
2014
Highly Cited
2014
Treatment of sickle cell disease (SCD) is hampered by incomplete understanding of pathways linking hemolysis to vaso-occlusion… Expand
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Highly Cited
2008
Highly Cited
2008
Background Since mature erythrocytes are terminally differentiated cells without nuclei and organelles, it is commonly thought… Expand
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Highly Cited
2008
Highly Cited
2008
BACKGROUND Glycohemoglobin (GHB), reported as hemoglobin (Hb) A(1c), is a marker of long-term glycemic control in patients with… Expand
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Highly Cited
2007
Highly Cited
2007
Sickle cell anemia (HbSS) is characterized by hypermetabolism, chronic inflammation, and increased oxidative stress, but the… Expand
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Highly Cited
2004
Highly Cited
2004
In recent years an important role has been ascribed to a reduced nitric oxide (NO) availability in the pathophysiology of sickle… Expand
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Highly Cited
2003
Highly Cited
2003
The purpose of the study was to examine endothelium-dependent and -independent vasodilation of conduit and resistance vessels in… Expand
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Highly Cited
2002
Highly Cited
2002
Hemoglobin E is very common in parts of Southeast Asia. The possible malaria protective effects of this and other inherited… Expand
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Highly Cited
2000
Highly Cited
2000
In sub-Saharan Africa, anaemia in pregnancy results from multiple causes including malaria, iron deficiency and… Expand
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Highly Cited
1999
Highly Cited
1999
Vascular occlusion is the main cause of the morbidity and mortality observed in patients with sickle cell disease (SCD… Expand
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