Hemoglobinopathies

Known as: Hemoglobinopathies [Disease/Finding], Hemoglobinopathy, HEMOGLOBIN DISORDER 
An inherited disorder characterized by structural alterations of a globin chain within the hemoglobin molecule.
National Institutes of Health

Papers overview

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Review
2017
Review
2017
BACKGROUND Haemoglobinopathies constitute the commonest recessive monogenic disorders worldwide, and the treatment of affected… (More)
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Highly Cited
2014
Highly Cited
2014
Previous studies of anemia epidemiology have been geographically limited with little detail about severity or etiology. Using… (More)
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Highly Cited
2011
Highly Cited
2011
BACKGROUND Iron deficiency anaemia (IDA) occurs in 2-5% of adult men and postmenopausal women in the developed world and is a… (More)
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Highly Cited
2006
Highly Cited
2006
Patients with sickle cell anemia (SCA) may develop a glomerulopathy with proteinuria and progressive renal insufficiency, leading… (More)
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Highly Cited
2004
Highly Cited
2004
BACKGROUND Previous evaluations of HPLC as a tool for detection of hemoglobin variants have done so within newborn-screening… (More)
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Highly Cited
2002
Highly Cited
2002
Pulmonary hypertension is one of the major causes of morbidity and mortality of patients with sickle cell hemoglobinopathy (SCH… (More)
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1986
1986
We analyzed 178 episodes of bacteremia that occurred during 13,771 patient-years of follow-up of 3451 patients with sickle… (More)
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Highly Cited
1986
Highly Cited
1986
Children with sickle cell anemia have an increased susceptibility to bacterial infections, especially to those caused by… (More)
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Highly Cited
1984
Highly Cited
1984
To determine the influence of hemoglobinopathy on growth and development, we examined the height, weight, and sexual maturation… (More)
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Highly Cited
1982
Highly Cited
1982
We describe a rapid procedure for constructing cloned human genomic libraries from small amounts of peripheral blood. High… (More)
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