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hemoglobin e disease

Known as: Hb E-disease, Hb-E disease, diseases e haemoglobin 
A condition characterized by the presence of a variant of normal hemoglobin (hemoglobin E), which is caused by mutation(s) in the gene encoding the… Expand
National Institutes of Health

Papers overview

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2015
2015
Glycosylated hemoglobin (HbA1C) is a routinely measured parameter to monitor long-term glycemic control in people with diabetes… Expand
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2007
2007
Beta-thalassemia/hemoglobin (Hb) E is a hereditary hemolytic anemia with varying degrees of severity. Severely affected patients… Expand
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Highly Cited
2005
Highly Cited
2005
Abstract The thalassemias are common monogenic disorders of hemoglobin synthesis. β-thalassemias are the most important among the… Expand
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Highly Cited
2004
Highly Cited
2004
Persistent levels of plasma nontransferrin bound iron (NTBI) have been associated with tissue iron overload and toxicity. We… Expand
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2003
2003
A correlation between endogenous hemin and pro-oxidant activity was revealed in serum of g -thalassemia/hemoglobin E disease ( g… Expand
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Highly Cited
1996
Highly Cited
1996
Hydroxyurea (HU) is one of several agents that have been shown to enhance hemoglobin (Hb) F levels in patients with sickle cell… Expand
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Review
1992
Review
1992
Chronic pulmonary thromboembolism plays an important role in cardiac failure which is a major cause of death in thalassemic… Expand
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1990
1990
We describe two Chinese patients with beta-thalassemia/hemoglobin E disease who developed cerebral infarction due to occlusion or… Expand
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1990
1990
Clinical and hemodynamic studies were conducted in 6 women and 2 men with beta-thalassemia/hemoglobin E disease. All except one… Expand
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1960
1960
1. A clinical and hematologic description is presented of a patient with sickle-cell-hemoglobin E disease in a new family. In… Expand
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