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Thalassemia
Known as:
Thalassemia, unspecified
, syndromes thalassemia
, Thalassemia [Disease/Finding]
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A group of hereditary hemolytic anemias in which there is decreased synthesis of one or more hemoglobin polypeptide chains. There are several genetic…
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National Institutes of Health
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Related topics
Related topics
25 relations
Anemia
Bart's Hemoglobinopathy
Hematological Disease
Hematopoietic and Lymphoid Cell
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Broader (2)
Anemia, Hemolytic, Congenital
Hemoglobinopathies
Narrower (6)
Cooley's anemia
Hemoglobin F Disease
Hereditary persistence of fetal hemoglobin thalassemia
Thalassemia Minor
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Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2007
2007
Exploring the Dirty Side of Women's Health
M. Kirkham
2007
Corpus ID: 68425533
1. Language and Status: The Disappearing and Reappearing 'Midwife' 2. Genetic Traits as Pollution: The Case of 'White English…
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Review
2003
Review
2003
Quantitative analysis of chimerism after allogeneic stem cell transplantation by PCR amplification of microsatellite markers and capillary electrophoresis with fluorescence detection: the Frankfurt…
Ulrike Koehl
,
Olaf Beck
,
+4 authors
Christian Seidl
Leukemia
2003
Corpus ID: 12472220
Quantitative analysis of chimerism after allogeneic stem cell transplantation by PCR amplification of microsatellite markers and…
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Highly Cited
1978
Highly Cited
1978
Lens opacities in thalassemia.
S. Bloomfield
,
A. Markenson
,
D. Miller
,
C. Peterson
Journal of pediatric ophthalmology and strabismus
1978
Corpus ID: 44904648
This is the first case report of cataracts in patients with thalassemia major. Desferrioxamine, an iron-chelating agent is being…
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1974
1974
Gene deletion as the cause of α thalassaemia: The severe form of α thalassaemia is caused by a haemoglobin gene deletion
S. Ottolenghi
,
W. Lanyon
,
+6 authors
W. H. Boon
Nature
1974
Corpus ID: 4253040
Two independent groups show that the absence of all or part of the globin α-chain gene is the origin of the homozygous…
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Highly Cited
1973
Highly Cited
1973
The clinical features of sickle-cell- thalassaemia in Jamaica.
G. R. Serjeant
,
M. T. Ashcroft
,
B. Serjeant
,
P. Milner
British Journal of Haematology
1973
Corpus ID: 33552931
Highly Cited
1973
Highly Cited
1973
Screening for thalassemia trait by electronic measurement of mean corpuscular volume.
H. Pearson
,
R. O'brien
,
S. Mcintosh
New England Journal of Medicine
1973
Corpus ID: 11361233
THALASSEMIAS are a group of hereditary blood conditions with clinical and genetic implications that occur frequently in…
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Highly Cited
1961
Highly Cited
1961
TAXONOMIC RELATIONSHIPS AMONG THE PSEUDOMONADS
R. Colwell
,
J. Liston
Journal of Bacteriology
1961
Corpus ID: 12052085
Colwell, R. R. (University of Washington, Seattle), and J. Liston. Taxonomic relationships among the pseudomonads. J. Bacteriol…
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Highly Cited
1961
Highly Cited
1961
Thalassemia in the West Indies.
L. Went
,
J. Maciver
Blood
1961
Corpus ID: 16193843
UNTIL comparatively recently thalassemia was thought to be confined predominantly to persons of Mediterranean origin. it is now…
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1954
1954
An abnormal substance present in the erythroblasts of thalassaemia major; cytochemical investigations.
G. Astaldi
,
E. Rondanelli
,
E. Bernardelli
,
E. Strosselli
Acta Haematologica
1954
Corpus ID: 46741452
Highly Cited
1944
Highly Cited
1944
HEMATOLOGIC AND GENETIC STUDY OF THE TRANSMISSION OF THALASSEMIA: (COOLEY'S ANEMIA; MEDITERRANEAN ANEMIA)
W. N. Valentine
,
J. Neel
1944
Corpus ID: 71785728
Cooley's anemia, 1 or thalassemia, 2 is a rare but well known disease. This fatal disorder is characterized by a chronic…
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