"Blood Platelet Disorders" 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.
Disorders caused by abnormalities in platelet count or function.
| Descriptor ID |
D001791
|
| MeSH Number(s) |
C15.378.140
|
| Concept/Terms |
Blood Platelet Disorders- Blood Platelet Disorders
- Blood Platelet Disorder
- Disorder, Blood Platelet
- Disorders, Blood Platelet
- Platelet Disorder, Blood
- Platelet Disorders, Blood
- Thrombocytopathy
- Thrombocytopathies
|
Below are MeSH descriptors whose meaning is more general than "Blood Platelet Disorders".
Below are MeSH descriptors whose meaning is more specific than "Blood Platelet Disorders".
This graph shows the total number of publications written about "Blood Platelet Disorders" by people in this website by year, and whether "Blood Platelet Disorders" was a major or minor topic of these publications.
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| Year | Major Topic | Minor Topic | Total |
|---|
| 2007 | 0 | 1 | 1 |
| 2010 | 1 | 0 | 1 |
| 2016 | 1 | 0 | 1 |
| 2017 | 0 | 1 | 1 |
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Below are the most recent publications written about "Blood Platelet Disorders" by people in Profiles.
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Mao GF, Goldfinger LE, Fan DC, Lambert MP, Jalagadugula G, Freishtat R, Rao AK. Dysregulation of PLDN (pallidin) is a mechanism for platelet dense granule deficiency in RUNX1 haplodeficiency. J Thromb Haemost. 2017 04; 15(4):792-801.
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Cuker A, Husseinzadeh H, Lebedeva T, Marturano JE, Massefski W, Lowery TJ, Lambert MP, Abrams CS, Weisel JW, Cines DB. Rapid Evaluation of Platelet Function With T2 Magnetic Resonance. Am J Clin Pathol. 2016 Dec; 146(6):681-693.
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Jalagadugula G, Mao G, Kaur G, Goldfinger LE, Dhanasekaran DN, Rao AK. Regulation of platelet myosin light chain (MYL9) by RUNX1: implications for thrombocytopenia and platelet dysfunction in RUNX1 haplodeficiency. Blood. 2010 Dec 23; 116(26):6037-45.
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Franke JD, Montague RA, Rickoll WL, Kiehart DP. An MYH9 human disease model in flies: site-directed mutagenesis of the Drosophila non-muscle myosin II results in hypomorphic alleles with dominant character. Hum Mol Genet. 2007 Dec 15; 16(24):3160-73.