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Thalassemia

Known as: Thalassemia, unspecified, syndromes thalassemia, Thalassemia [Disease/Finding] 
A group of hereditary hemolytic anemias in which there is decreased synthesis of one or more hemoglobin polypeptide chains. There are several genetic… 
National Institutes of Health

Related topics

Related topics

25 relations
AnemiaBart's HemoglobinopathyHematological DiseaseHematopoietic and Lymphoid Cell

Broader (2)

Anemia, Hemolytic, CongenitalHemoglobinopathies

Narrower (6)

Cooley's anemiaHemoglobin F DiseaseHereditary persistence of fetal hemoglobin thalassemiaThalassemia Minor

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
Highly Cited
1996
Highly Cited
1996
Dissecting the loci controlling fetal haemoglobin production on chromosomes 11p and 6q by the regressive approach
The Changes in the type of haemoglobin (Hb) produced during embryonic, fetal and adult life, have served as a paradigm for… 
Highly Cited
1995
Highly Cited
1995
Assessment of liver iron overload by T2-quantitative magnetic resonance imaging: correlation of T2-QMRI measurements with serum ferritin concentration and histologic grading of siderosis.
Highly Cited
1993
Highly Cited
1993
Frequency of anti-recipient alloreactive helper T-cell precursors in donor blood and graft-versus-host disease after HLA-identical sibling bone-marrow transplantation
Review
1992
Review
1992
Of mice and men: Genetic skin diseases of keratin
Highly Cited
1990
Highly Cited
1990
Molecular analysis of deletions in the human beta-globin gene cluster: deletion junctions and locations of breakpoints.
Review
1984
Review
1984
Investigation of nonimmune hydrops fetalis.
Highly Cited
1984
Highly Cited
1984
Ocular changes in patients undergoing long-term desferrioxamine treatment.
In a group of young patients with thalassaemia and iron overload treated by subcutaneous infusions of desferrioxamine we have… 
Highly Cited
1970
Highly Cited
1970
Two Haemoglobins Q, α74 (EF3) and α75 (EF4) Aspartic Acid→Histidine
Summary Six samples of Haemoglobin Q were examined, three from Iran, two from Thailand, and one from California (Chinese). They… 
Highly Cited
1966
Highly Cited
1966
Excess α Chain Synthesis Relative to β Chain Synthesis in Thalassaemia Major and Minor
Highly Cited
1962
Highly Cited
1962
Types of Thalassaemia‐Trait Carriers as Revealed by a Study of their Incidence in Greece
ALTHOUGH the frequent occurrence of thalassaemia and its hereditary nature havc been recognized for many years in Greecc… 
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