Anemia, Hemolytic, Congenital
"Anemia, Hemolytic, Congenital" 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.
Hemolytic anemia due to various intrinsic defects of the erythrocyte.
MeSH Number(s)
C15.378.071.141.150
C16.320.070
Concept/Terms
Anemia, Hemolytic, Congenital- Anemia, Hemolytic, Congenital
- Hemolytic Anemia, Congenital
- Anemia, Hemolytic, Hereditary
- Hemolytic Anemia, Hereditary
- Anemia, Hereditary Hemolytic
- Anemias, Hereditary Hemolytic
- Hemolytic Anemias, Hereditary
- Hereditary Hemolytic Anemias
- Hereditary Hemolytic Anemia
- Congenital Hemolytic Anemia
- Anemia, Congenital Hemolytic
- Anemias, Congenital Hemolytic
- Congenital Hemolytic Anemias
- Hemolytic Anemias, Congenital
Below are MeSH descriptors whose meaning is more general than "Anemia, Hemolytic, Congenital".
Below are MeSH descriptors whose meaning is more specific than "Anemia, Hemolytic, Congenital".
This graph shows the total number of publications written about "Anemia, Hemolytic, Congenital" by people in Harvard Catalyst Profiles by year, and whether "Anemia, Hemolytic, Congenital" was a major or minor topic of these publication.
To see the data from this visualization as text,
click here.
Year | Major Topic | Minor Topic | Total |
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2001 | 1 | 0 | 1 |
2003 | 1 | 0 | 1 |
2007 | 1 | 0 | 1 |
2009 | 2 | 0 | 2 |
2010 | 1 | 0 | 1 |
2011 | 0 | 1 | 1 |
2012 | 1 | 0 | 1 |
2013 | 3 | 0 | 3 |
2014 | 3 | 0 | 3 |
2015 | 1 | 0 | 1 |
2016 | 1 | 0 | 1 |
2017 | 2 | 0 | 2 |
2018 | 1 | 0 | 1 |
2019 | 4 | 0 | 4 |
2021 | 1 | 0 | 1 |
2022 | 3 | 0 | 3 |
Below are the most recent publications written about "Anemia, Hemolytic, Congenital" by people in Profiles.
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Glucose 6 Phosphate Isomerase Deficiency, a Rare Hemolytic Anemia Misdiagnosed as Hereditary Spherocytosis. J Pediatr Hematol Oncol. 2023 01 01; 45(1):41-43.
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Hereditary anemia caused by multilocus inheritance of PIEZO1, SLC4A1 and ABCB6 mutations: a diagnostic and therapeutic challenge. Haematologica. 2022 09 01; 107(9):2280-2284.
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PIEZO1, sensing the touch during erythropoiesis. Curr Opin Hematol. 2022 05 01; 29(3):112-118.
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Recent advances in the pathophysiology of PIEZO1-related hereditary xerocytosis. Am J Hematol. 2021 08 01; 96(8):1017-1026.
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PIEZO1 activation delays erythroid differentiation of normal and hereditary xerocytosis-derived human progenitor cells. Haematologica. 2020 03; 105(3):610-622.
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Anemia predicts lower white matter volume and cognitive performance in sickle and non-sickle cell anemia syndrome. Am J Hematol. 2019 10; 94(10):1055-1065.
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Erythrocyte ion content and dehydration modulate maximal Gardos channel activity in KCNN4 V282M/+ hereditary xerocytosis red cells. Am J Physiol Cell Physiol. 2019 08 01; 317(2):C287-C302.
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Aberrant splicing contributes to severe a-spectrin-linked congenital hemolytic anemia. J Clin Invest. 2019 04 30; 129(7):2878-2887.
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Genotype-phenotype correlation and risk stratification in a cohort of 123 hereditary stomatocytosis patients. Am J Hematol. 2018 12; 93(12):1509-1517.
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Common PIEZO1 Allele in African Populations Causes RBC Dehydration and Attenuates Plasmodium Infection. Cell. 2018 04 05; 173(2):443-455.e12.