"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 |
|---|
| 1997 | 1 | 0 | 1 |
| 2002 | 1 | 0 | 1 |
| 2015 | 1 | 0 | 1 |
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Below are the most recent publications written about "Hemoglobinopathies" by people in Profiles.
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Enayatollahi MA, Novack TA, Maltenfort MG, Tabatabaee RM, Chen AF, Parvizi J. In-Hospital Morbidity and Mortality Following Total Joint Arthroplasty in Patients with Hemoglobinopathies. J Arthroplasty. 2015 Aug; 30(8):1308-12.
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Heeney MM, Delgrosso K, Robinson R, Johnson CA, Daeschner CW, Campbell TA, Surrey S, Ware RE. Interpretation of fetal hemoglobin only on newborn screening for hemoglobinopathy. J Pediatr Hematol Oncol. 2002 Aug-Sep; 24(6):499-502.
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Camaschella C, Kattamis AC, Petroni D, Roetto A, Sivera P, Sbaiz L, Cohen A, Ohene-Frempong K, Trifillis P, Surrey S, Fortina P. Different hematological phenotypes caused by the interaction of triplicated alpha-globin genes and heterozygous beta-thalassemia. Am J Hematol. 1997 Jun; 55(2):83-8.
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Gumucio DL, Lockwood WK, Weber JL, Saulino AM, Delgrosso K, Surrey S, Schwartz E, Goodman M, Collins FS. The -175T----C mutation increases promoter strength in erythroid cells: correlation with evolutionary conservation of binding sites for two trans-acting factors. Blood. 1990 Feb 01; 75(3):756-61.
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Surrey S, Delgrosso K, Malladi P, Schwartz E. A single-base change at position -175 in the 5'-flanking region of the G gamma-globin gene from a black with G gamma-beta+ HPFH. Blood. 1988 Mar; 71(3):807-10.
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Schwartz E, Month S, Delgrosso K, Rappaport E, Orchowski P, Malladi P, Surrey S. DNA sequence changes in the 5'-flanking region of G gamma-globin genes in a black with beta S and a non-deletional form of G gamma-beta+ HPFH. Prog Clin Biol Res. 1987; 251:363-71.