"Anemia, Megaloblastic" 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 disorder characterized by the presence of ANEMIA, abnormally large red blood cells (megalocytes or macrocytes), and MEGALOBLASTS.
| Descriptor ID |
D000749
|
| MeSH Number(s) |
C15.378.071.252.196
|
| Concept/Terms |
Anemia, Megaloblastic- Anemia, Megaloblastic
- Anemias, Megaloblastic
- Megaloblastic Anemia
- Megaloblastic Anemias
|
Below are MeSH descriptors whose meaning is more general than "Anemia, Megaloblastic".
Below are MeSH descriptors whose meaning is more specific than "Anemia, Megaloblastic".
This graph shows the total number of publications written about "Anemia, Megaloblastic" by people in this website by year, and whether "Anemia, Megaloblastic" was a major or minor topic of these publications.
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| Year | Major Topic | Minor Topic | Total |
|---|
| 2018 | 1 | 0 | 1 |
| 2019 | 1 | 0 | 1 |
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Below are the most recent publications written about "Anemia, Megaloblastic" by people in Profiles.
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50 Years Ago in The Journal of Pediatrics: Thiamine-Responsive Megaloblastic Anemia. J Pediatr. 2019 04; 207:53.
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Megaloblastic Anemia Progressing to Severe Thrombotic Microangiopathy in Patients with Disordered Vitamin B12 Metabolism: Case Reports and Literature Review. J Pediatr. 2018 11; 202:315-319.e2.
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Genetically heterogeneous selective intestinal malabsorption of vitamin B12: founder effects, consanguinity, and high clinical awareness explain aggregations in Scandinavia and the Middle East. Hum Mutat. 2004 Apr; 23(4):327-33.
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Cubilin P1297L mutation associated with hereditary megaloblastic anemia 1 causes impaired recognition of intrinsic factor-vitamin B(12) by cubilin. Blood. 2000 Jul 15; 96(2):405-9.
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The intrinsic factor-vitamin B12 receptor, cubilin, is a high-affinity apolipoprotein A-I receptor facilitating endocytosis of high-density lipoprotein. Nat Med. 1999 Jun; 5(6):656-61.
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Mutations in CUBN, encoding the intrinsic factor-vitamin B12 receptor, cubilin, cause hereditary megaloblastic anaemia 1. Nat Genet. 1999 Mar; 21(3):309-13.