"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
|
| MeSH Number(s) |
C15.378.420 C16.320.365
|
| Concept/Terms |
|
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 |
|---|
| 1998 | 1 | 0 | 1 |
| 2012 | 1 | 0 | 1 |
| 2013 | 1 | 0 | 1 |
| 2015 | 2 | 0 | 2 |
| 2017 | 1 | 0 | 1 |
| 2018 | 0 | 1 | 1 |
| 2019 | 2 | 0 | 2 |
| 2020 | 1 | 0 | 1 |
| 2021 | 1 | 0 | 1 |
| 2023 | 2 | 0 | 2 |
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click here.
Below are the most recent publications written about "Hemoglobinopathies" by people in Profiles.
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C2H2 Zinc Finger Transcription Factors Associated with Hemoglobinopathies. J Mol Biol. 2024 Apr 01; 436(7):168343.
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Unique Hemoglobinopathy Pattern Following Treatment with Voxelotor. Ann Clin Lab Sci. 2023 Jul; 53(4):647-652.
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Hemoglobin fractionation by Sebia Capillarys 2 Flex Piercing System as primary method for evaluation of hemoglobinopathies. Clin Chim Acta. 2021 Aug; 519:193-197.
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Misidentification of unstable, low oxygen affinity hemoglobin variant. Clin Chim Acta. 2020 Oct; 509:177-179.
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Microbiology of Osteoarticular Infections in Patients with Sickle Hemoglobinopathies at Texas Children's Hospital, 2000-2018. Pediatr Infect Dis J. 2019 12; 38(12):1251-1253.
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Effect of increased dose of total body irradiation on graft failure associated with HLA-haploidentical transplantation in patients with severe haemoglobinopathies: a prospective clinical trial. Lancet Haematol. 2019 Apr; 6(4):e183-e193.
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Compound Heterozygosity for Hb D-Ibadan (HBB: c.263C>A) and Hb C (HBB: c.19G>A). Hemoglobin. 2018 Jul; 42(4):269-271.
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Proceedings From the Fourth Haploidentical Stem Cell Transplantation Symposium (HAPLO2016), San Diego, California, December 1, 2016. Biol Blood Marrow Transplant. 2018 05; 24(5):895-908.
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Establishing an autologous versus allogeneic hematopoietic cell transplant program in nations with emerging economies. Hematol Oncol Stem Cell Ther. 2017 Dec; 10(4):173-177.
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Successful matched sibling donor marrow transplantation following reduced intensity conditioning in children with hemoglobinopathies. Am J Hematol. 2015 Dec; 90(12):1093-8.