"Hemoglobins, 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.
Hemoglobins characterized by structural alterations within the molecule. The alteration can be either absence, addition or substitution of one or more amino acids in the globin part of the molecule at selected positions in the polypeptide chains.
| Descriptor ID |
D006455
|
| MeSH Number(s) |
D12.776.124.400.463 D12.776.422.316.762.426
|
| Concept/Terms |
|
Below are MeSH descriptors whose meaning is more general than "Hemoglobins, Abnormal".
Below are MeSH descriptors whose meaning is more specific than "Hemoglobins, Abnormal".
This graph shows the total number of publications written about "Hemoglobins, Abnormal" by people in this website by year, and whether "Hemoglobins, Abnormal" was a major or minor topic of these publications.
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| Year | Major Topic | Minor Topic | Total |
|---|
| 2005 | 0 | 2 | 2 |
| 2007 | 2 | 0 | 2 |
| 2009 | 1 | 0 | 1 |
| 2020 | 1 | 0 | 1 |
| 2021 | 1 | 0 | 1 |
| 2024 | 1 | 0 | 1 |
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Below are the most recent publications written about "Hemoglobins, Abnormal" by people in Profiles.
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Pediatric case of hemoglobin I-high Wycombe variant. Clin Chim Acta. 2025 Feb 01; 567:120098.
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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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The clinical and laboratory spectrum of Hb C [?6(A3)Glu?Lys, GAG>AAG] disease. Hemoglobin. 2013; 37(1):16-25.
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The diagnostic dilemma of congenital unstable hemoglobinopathies. Pediatr Blood Cancer. 2010 Dec 15; 55(7):1393-5.
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Homozygous alpha-thalassemia treated with intrauterine transfusions and unrelated donor hematopoietic cell transplantation. J Pediatr. 2009 May; 154(5):766-8.
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Missense mutation of the last nucleotide of exon 1 (G->C) of beta globin gene not only leads to undetectable mutant peptide and transcript but also interferes with the expression of wild allele. Haematologica. 2007 Dec; 92(12):1715-6.
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Sickle cell disease caused by Hb S/Qu?bec-CHORI: treatment with hydroxyurea and response. Pediatr Blood Cancer. 2007 Aug; 49(2):207-10.
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Thromboelastographic and hemostatic characteristics in pediatric patients with sickle cell disease. Arch Pathol Lab Med. 2005 Jun; 129(6):760-5.
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ATR-16 due to a de novo complex rearrangement of chromosome 16. Hemoglobin. 2005; 29(2):141-50.