"alpha-Thalassemia" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus,
MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure,
which enables searching at various levels of specificity.
A disorder characterized by reduced synthesis of the alpha chains of hemoglobin. The severity of this condition can vary from mild anemia to death, depending on the number of genes deleted.
Descriptor ID |
D017085
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MeSH Number(s) |
C15.378.071.141.150.875.100 C15.378.420.826.100 C16.320.070.875.100 C16.320.365.826.100
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Concept/Terms |
alpha-Thalassemia- alpha-Thalassemia
- alpha-Thalassemias
- Alpha Thalassemia
- Thalassemia, Alpha
- Thalassemia-alpha
- Thalassemia alpha
- A-Thalassemia
- Hemoglobin H Disease
- Disease, Hemoglobin H
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Below are MeSH descriptors whose meaning is more general than "alpha-Thalassemia".
Below are MeSH descriptors whose meaning is more specific than "alpha-Thalassemia".
This graph shows the total number of publications written about "alpha-Thalassemia" by people in this website by year, and whether "alpha-Thalassemia" was a major or minor topic of these publications.
To see the data from this visualization as text,
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Year | Major Topic | Minor Topic | Total |
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2010 | 1 | 0 | 1 |
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Below are the most recent publications written about "alpha-Thalassemia" by people in Profiles.
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Wilburn CR, Bernard DW, Zieske AW, Andrieni J, Miller T, Wang P. The Prevalence and Role of Hemoglobin Variants in Biometric Screening of a Multiethnic Population: One Large Health System's Experience. Am J Clin Pathol. 2017 Jun 01; 147(6):589-595.
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Switzer WM, Shankar A, Trimble SR, Thompson AA, Giardina PJ, Cohen AR, Coates TD, Vichinsky E, Neufeld EJ, Boudreaux JM, Heneine W. Human T cell lymphotropic virus type 1 infection among U.S. thalassemia patients. AIDS Res Hum Retroviruses. 2013 Jul; 29(7):1006-9.
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Kemper AR, Knapp AA, Metterville DR, Comeau AM, Green NS, Perrin JM. Weighing the evidence for newborn screening for Hemoglobin H disease. J Pediatr. 2011 May; 158(5):780-3.
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Singer ST, Kim HY, Olivieri NF, Kwiatkowski JL, Coates TD, Carson S, Neufeld E, Cunningham MJ, Giardina PJ, Mueller BU, Quinn CT, Fung E, Vichinsky E. Hemoglobin H-constant spring in North America: an alpha thalassemia with frequent complications. Am J Hematol. 2009 Nov; 84(11):759-61.