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Hemoglobin SC Disease

Known as: Disease, SC, hemoglobin s-c disease, Hemoglobin SC Diseases 
A hemoglobinopathy that is considered a hybrid of sickle cell disease and hemoglobin C disease. Patients present with the symptoms of sickle cell… Expand
National Institutes of Health

Papers overview

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Highly Cited
2010
Highly Cited
2010
Hereditary persistence of fetal hemoglobin (HPFH) is characterized by persistent high levels of fetal hemoglobin (HbF) in adults… Expand
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Highly Cited
2008
Highly Cited
2008
Differences in the amount of fetal hemoglobin (HbF) that persists into adulthood affect the severity of sickle cell disease and… Expand
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Highly Cited
2008
Highly Cited
2008
Sickle cell disease (SCD) is a debilitating monogenic blood disorder with a highly variable phenotype characterized by severe… Expand
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Highly Cited
2008
Highly Cited
2008
BACKGROUND AIMS:Anemia is a common complication of inflammatory bowel diseases (IBD) This multicenter study tested the… Expand
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Highly Cited
1995
Highly Cited
1995
BACKGROUND In a previous open-label study of hydroxyurea therapy, the synthesis of fetal hemoglobin increased in most patients… Expand
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Highly Cited
1994
Highly Cited
1994
BACKGROUND The high relative mortality among patients with insulin-dependent diabetes mellitus results mainly from diabetic… Expand
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Highly Cited
1991
Highly Cited
1991
BACKGROUND AND METHODS Acute episodes of pain are the principal symptom of sickle cell disease, but little is known about the… Expand
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Highly Cited
1989
Highly Cited
1989
Denaturing gradient gel electrophoresis (DGGE) can be used to distinguish two DNA molecules that differ by as little as a single… Expand
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Highly Cited
1988
Highly Cited
1988
The relationship between hyperglycemia, measured by glycosylated hemoglobin at the initial examination, and the four-year… Expand
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Highly Cited
1971
Highly Cited
1971
Cells of a cloned line of murine virus-induced erythroleukemia were stimulated to differentiate along the erythroid pathway by… Expand
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