Hemoglobinopathies
"Hemoglobinopathies" 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 group of inherited disorders characterized by structural alterations within the hemoglobin molecule.
Descriptor ID |
D006453
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MeSH Number(s) |
C15.378.420 C16.320.365
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Concept/Terms |
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Below are MeSH descriptors whose meaning is more general than "Hemoglobinopathies".
Below are MeSH descriptors whose meaning is more specific than "Hemoglobinopathies".
This graph shows the total number of publications written about "Hemoglobinopathies" by people in this website by year, and whether "Hemoglobinopathies" 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 |
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2014 | 1 | 0 | 1 | 2019 | 1 | 0 | 1 | 2022 | 1 | 0 | 1 | 2023 | 1 | 0 | 1 |
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Below are the most recent publications written about "Hemoglobinopathies" by people in Profiles.
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Dampier CD, Telen MJ, Wun T, Brown RC, Desai P, El Rassi F, Fuh B, Kanter J, Pastore Y, Rothman J, Taylor JG, Readett D, Sivamurthy KM, Tammara B, Tseng LJ, Lozier JN, Thackray H, Magnani JL, Hassell KL. A randomized clinical trial of the efficacy and safety of rivipansel for sickle cell vaso-occlusive crisis. Blood. 2023 01 12; 141(2):168-179.
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Hazegh K, Fang F, Kelly K, Sinchar D, Wang L, Zuchelkowski BE, Ufelle AC, Esparza O, Davizon-Castillo P, Page GP, Kanias T. Erythrocyte mitogen-activated protein kinases mediate hemolytic events under osmotic and oxidative stress and in hemolytic diseases. Cell Signal. 2022 11; 99:110450.
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Putra M, Kaseniit KE, Hicks MA, Muzzey D, Hackney D. The impact of HBB-related hemoglobinopathies carrier status on fetal fraction in noninvasive prenatal screening. Prenat Diagn. 2022 04; 42(4):524-529.
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Putra M, Idler J, Patek K, Contos G, Walker C, Olson D, Hicks MA, Chaperon J, Korzeniewski SJ, Patwardhan SC, Sokol RJ. The association of HBB-related significant hemoglobinopathies and low fetal fraction on noninvasive prenatal screening for fetal aneuploidy. J Matern Fetal Neonatal Med. 2021 Nov; 34(22):3657-3661.
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Kent MW, Oliveira JL, Hoyer JD, Swanson KC, Kluge ML, Dawson DB, Liang X, Winkler TJ, Breaux CW, LaCount R, Silliman CC. Hb Grand Junction (HBB: c.348_349delinsG; p.His117IlefsX42): a new hyperunstable hemoglobin variant. Hemoglobin. 2014; 38(1):8-12.
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Ahmed F, Janes GR, Baron R, Latts LM. Preferred provider organization claims showed high predictive value but missed substantial proportion of adults with high-risk conditions. J Clin Epidemiol. 2005 Jun; 58(6):624-8.
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Peters C, Miller J, Abel SL, McMillan SK, Getchell JP, Giller RH, Hohl RJ, de Alarcon PA. Iowa newborn hemoglobinopathy screening and comprehensive care: a model for rural states. J Pediatr Hematol Oncol. 1996 Nov; 18(4):416-8.
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DeVore GR, Mahoney MJ, Hobbins JC. Antenatal diagnosis of haemoglobinopathies, haemophilia, von Willebrand's disease, Duchenne's muscular dystrophy, and chronic granulomatous disease by fetal blood analysis. Clin Obstet Gynaecol. 1980 Apr; 7(1):41-72.
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Hobbins JC, Mahoney MJ. Fetoscopy in continuing pregnancies. Am J Obstet Gynecol. 1977 Oct 15; 129(4):440-2.
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Chang H, Hobbins JC, Cividalli G, Frigoletto FD, Mahoney MJ, Kan YW, Nathan DG. In utero diagnosis of hemoglobinopathies. Hemoglobin synthesis in fetal red cells. N Engl J Med. 1974 05 09; 290(19):1067-8.
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