Thalassemia Intermedia

Known as: Intermedia, Thalassemia, Thalassemia Intermedias, Intermedias, Thalassemia 
 
National Institutes of Health

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Review
2011
Review
2011
Our understanding of the molecular and pathophysiological mechanisms underlying the disease process in patients with… (More)
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2011
2011
BACKGROUND Pulmonary hypertension (PHT) is a common yet poorly understood complication of β thalassemia intermedia (TI… (More)
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Highly Cited
2010
Highly Cited
2010
BACKGROUND  Hypercoagulability in splenectomized patients with thalassemia intermedia (TI) has been extensively evaluated… (More)
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Review
2009
Review
2009
Thalassemia intermedia (TI) presents with a clinical phenotype ranging between the severe, transfusion-dependent TM and the… (More)
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2008
2008
Introduction b-Thalassemia major (TM) and thalassemia intermedia (TI) are forms of inherited hemoglobinopathies. Our aim was to… (More)
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2007
2007
BACKGROUND beta-Thalassemia is an inherited hemoglobin disorder characterized by reduced synthesis of beta-globin chain. The… (More)
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2006
2006
Adult thalassemic patients have reduced bone mass due to disturbances in several different mechanisms affecting bone turnover. To… (More)
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Highly Cited
2005
Highly Cited
2005
BACKGROUND Heart disease represents the main determinant of survival in beta-thalassemia, but its particular features in the two… (More)
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Review
1995
Review
1995
Thalassemia intermedia is a clinical definition applied to patients whose clinical phenotype is milder than that of thalassemia… (More)
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Highly Cited
1967
Highly Cited
1967
Thalassemias are a group of hereditary anaemias which are prevalent in the Mediterranean countries, the Middle East and Asia… (More)
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