"Erythrocytes, Abnormal" 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.
Oxygen-carrying RED BLOOD CELLS in mammalian blood that are abnormal in structure or function.
Descriptor ID |
D004913
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MeSH Number(s) |
A11.118.290.330 A11.443.240.330 A15.145.229.334.330
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Concept/Terms |
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Below are MeSH descriptors whose meaning is more general than "Erythrocytes, Abnormal".
Below are MeSH descriptors whose meaning is more specific than "Erythrocytes, Abnormal".
This graph shows the total number of publications written about "Erythrocytes, Abnormal" by people in this website by year, and whether "Erythrocytes, Abnormal" was a major or minor topic of these publications.
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click here.
Year | Major Topic | Minor Topic | Total |
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2016 | 1 | 0 | 1 |
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Below are the most recent publications written about "Erythrocytes, Abnormal" by people in Profiles.
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Gordeuk VR. Sickle cell vaso-occlusion: the clot thickens. Blood. 2020 05 14; 135(20):1726-1727.
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Raffield LM, Ulirsch JC, Naik RP, Lessard S, Handsaker RE, Jain D, Kang HM, Pankratz N, Auer PL, Bao EL, Smith JD, Lange LA, Lange EM, Li Y, Thornton TA, Young BA, Abecasis GR, Laurie CC, Nickerson DA, McCarroll SA, Correa A, Wilson JG, Lettre G, Sankaran VG, Reiner AP. Common a-globin variants modify hematologic and other clinical phenotypes in sickle cell trait and disease. PLoS Genet. 2018 03; 14(3):e1007293.
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Dai Y, Sangerman J, Nouraie M, Faller AD, Oneal P, Rock A, Owoyemi O, Niu X, Nekhai S, Maharaj D, Cui S, Taylor R, Steinberg M, Perrine S. Effects of hydroxyurea on F-cells in sickle cell disease and potential impact of a second fetal globin inducer. Am J Hematol. 2017 Jan; 92(1):E10-E11.
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Ekong DE, Okogun JI, Enyenihi VU, Balogh-Nair V, Nakanishi K, Natta C. New antisickling agent 3,4-dihydro-2,2-dimethyl-2h-1 benzopyran-6-butyric acid. Nature. 1975 Dec 25; 258(5537):743-6.
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Kwiatkowska J. [Erythrocyte metabolism in hereditary spherocytosis]. Acta Haematol Pol. 1971 Apr-Jun; 2(2):187-93.