 beta-Thalassemia
"beta-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 beta chains of hemoglobin. There is retardation of hemoglobin A synthesis in the heterozygous form (thalassemia minor), which is asymptomatic, while in the homozygous form (thalassemia major, Cooley's anemia, Mediterranean anemia, erythroblastic anemia), which can result in severe complications and even death, hemoglobin A synthesis is absent.
| Descriptor ID |
D017086
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| MeSH Number(s) |
C15.378.071.141.150.875.150 C15.378.420.826.150 C16.320.070.875.150 C16.320.365.826.150
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| Concept/Terms |
beta-Thalassemia- beta-Thalassemia
- Microcytemia, beta Type
- Microcytemias, beta Type
- Type Microcytemia, beta
- Type Microcytemias, beta
- beta Type Microcytemia
- beta Type Microcytemias
- beta Thalassemia
- Thalassemia, beta
- Thalassemias, beta
- beta Thalassemias
- Thalassemia, beta Type
- Thalassemias, beta Type
- Type Thalassemia, beta
- Type Thalassemias, beta
- beta Type Thalassemia
- beta Type Thalassemias
Thalassemia Intermedia- Thalassemia Intermedia
- Intermedia, Thalassemia
- Intermedias, Thalassemia
- Thalassemia Intermedias
Thalassemia Minor- Thalassemia Minor
- Thalassemia Minor (beta-Thalassemia Minor)
- Minor, Thalassemia (beta-Thalassemia Minor)
- Minors, Thalassemia (beta-Thalassemia Minor)
- Thalassemia Minor (beta Thalassemia Minor)
- Thalassemia Minors (beta-Thalassemia Minor)
Thalassemia Major- Thalassemia Major
- Anemia, Erythroblastic
- Anemias, Erythroblastic
- Erythroblastic Anemia
- Thalassemia Major (beta-Thalassemia Major)
- Major, Thalassemia (beta-Thalassemia Major)
- Majors, Thalassemia (beta-Thalassemia Major)
- Thalassemia Major (beta Thalassemia Major)
- Thalassemia Majors (beta-Thalassemia Major)
- Mediterranean Anemia
- Anemias, Mediterranean
- Mediterranean Anemias
- Anemia, Cooley's
- Anemia, Cooley
- Anemia, Cooleys
- Cooley's Anemia
- Anemia, Mediterranean
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Below are MeSH descriptors whose meaning is more general than "beta-Thalassemia".
Below are MeSH descriptors whose meaning is more specific than "beta-Thalassemia".
This graph shows the total number of publications written about "beta-Thalassemia" by people in this website by year, and whether "beta-Thalassemia" was a major or minor topic of these publications.
To see the data from this visualization as text, click here.
| Year | Major Topic | Minor Topic | Total |
|---|
| 1994 | 1 | 0 | 1 | | 1997 | 1 | 0 | 1 | | 2003 | 1 | 0 | 1 | | 2006 | 0 | 1 | 1 | | 2013 | 1 | 0 | 1 | | 2015 | 1 | 0 | 1 | | 2018 | 1 | 0 | 1 | | 2021 | 2 | 0 | 2 | | 2022 | 1 | 0 | 1 | | 2023 | 2 | 0 | 2 |
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Below are the most recent publications written about "beta-Thalassemia" by people in Profiles.
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Hurtado J, Sellak H, Joseph G, Lewis CV, Naudin CR, Garcia S, Wodicka JR, Archer DR, Taylor WR. Accelerated atherosclerosis in beta-thalassemia. Am J Physiol Heart Circ Physiol. 2023 11 01; 325(5):H1133-H1143.
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Lisk C, Cendali F, Setua S, Thangaraju K, Pak DI, Swindle D, Dzieciatkowska M, Gamboni F, Hassell K, Nuss R, George G, Davizon-Castillo P, Buehler PW, D'Alessandro A, Irwin DC. Metabolic and Proteomic Divergence Is Present in Circulating Monocytes and Tissue-Resident Macrophages from Berkeley Sickle Cell Anemia and ?-Thalassemia Mice. J Proteome Res. 2023 09 01; 22(9):2925-2935.
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Tzounakas VL, Anastasiadi AT, Stefanoni D, Cendali F, Bertolone L, Gamboni F, Dzieciatkowska M, Rousakis P, Vergaki A, Soulakis V, Tsitsilonis OE, Stamoulis K, Papassideri IS, Kriebardis AG, D'Alessandro A, Antonelou MH. Beta thalassemia minor is a beneficial determinant of red blood cell storage lesion. Haematologica. 2022 01 01; 107(1):112-125.
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Anastasiadi AT, Paronis EC, Arvaniti VZ, Velentzas AD, Apostolidou AC, Balafas EG, Dzieciatkowska M, Kostomitsopoulos NG, Stamoulis K, Papassideri IS, D'Alessandro A, Kriebardis AG, Antonelou MH, Tzounakas VL. The Post-Storage Performance of RBCs from Beta-Thalassemia Trait Donors Is Related to Their Storability Profile. Int J Mol Sci. 2021 Nov 13; 22(22).
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Tzounakas VL, Anastasiadi AT, Dzieciatkowska M, Karadimas DG, Stamoulis K, Papassideri IS, Hansen KC, D'Alessandro A, Kriebardis AG, Antonelou MH. Proteome of Stored RBC Membrane and Vesicles from Heterozygous Beta Thalassemia Donors. Int J Mol Sci. 2021 Mar 25; 22(7).
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Lal A, Wong TE, Andrews J, Balasa VV, Chung JH, Forester CM, Ikeda AK, Keel SB, Pagano MB, Puthenveetil G, Shah SJ, Yu JC, Vichinsky EP. Transfusion practices and complications in thalassemia. Transfusion. 2018 12; 58(12):2826-2835.
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Vallelian F, Gelderman-Fuhrmann MP, Schaer CA, Puglia M, Opitz L, Baek JH, Vostal J, Buehler PW, Schaer DJ. Integrative proteome and transcriptome analysis of extramedullary erythropoiesis and its reversal by transferrin treatment in a mouse model of beta-thalassemia. J Proteome Res. 2015 Feb 06; 14(2):1089-100.
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Danjou F, Origa R, Anni F, Saba L, Cossa S, Podda G, Galanello R. Longitudinal analysis of heart and liver iron in thalassemia major patients according to chelation treatment. Blood Cells Mol Dis. 2013 Oct; 51(3):142-5.
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Field JJ, Strunk RC, Knight-Perry JE, Blinder MA, Townsend RR, DeBaun MR. Urinary cysteinyl leukotriene E4 significantly increases during pain in children and adults with sickle cell disease. Am J Hematol. 2009 Apr; 84(4):231-3.
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Mandava N, Bartlett H, Young LH, Brooks HL. Diagnostic and therapeutic challenges. Retina. 2006 Feb; 26(2):214-8.
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