"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 |
| 2011 | 2 | 0 | 2 |
| 2012 | 1 | 0 | 1 |
| 2015 | 1 | 0 | 1 |
| 2022 | 1 | 0 | 1 |
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Below are the most recent publications written about "Blood Platelet Disorders" by people in Profiles.
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Efficacy of novel agents against cellular models of familial platelet disorder with myeloid malignancy (FPD-MM). Blood Cancer J. 2024 02 05; 14(1):25.
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Acute myeloid leukemia in a child with familial platelet disorder and a cryptic runx1 intragenic deletion. Pediatr Hematol Oncol. 2022 09; 39(6):580-585.
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The RUNX1 database (RUNX1db): establishment of an expert curated RUNX1 registry and genomics database as a public resource for familial platelet disorder with myeloid malignancy. Haematologica. 2021 11 01; 106(11):3004-3007.
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Intrauterine Foley Balloon Catheter to Manage Acute Heavy Menstrual Bleeding in a Perimenarchal 10-Year-Old Girl. Obstet Gynecol. 2019 07; 134(1):77-80.
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Bone marrow pathologic abnormalities in familial platelet disorder with propensity for myeloid malignancy and germline RUNX1 mutation. Haematologica. 2017 10; 102(10):1661-1670.
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Systemic Inflammatory Response Syndrome After Contentious-Flow Left Ventricular Assist Device Implantation and Change in Platelet Mitochondrial Membrane Potential. J Card Fail. 2015 Jul; 21(7):564-71.
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It is not always immune thrombocytopenia: a case of MYH9-related platelet disorder caused by a novel mutation. Eur J Haematol. 2013 Aug; 91(2):191-2.
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Platelet function disorders and menorrhagia in adolescents: a review of laboratory diagnosis. J Pediatr Adolesc Gynecol. 2012 Aug; 25(4):233-7.
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Coagulation abnormalities in children undergoing epilepsy surgery. J Neurosurg Pediatr. 2011 Jun; 7(6):654-9.
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Extensive thrombosis and first-trimester pregnancy loss caused by sticky platelet syndrome. Obstet Gynecol. 2011 Feb; 117(2 Pt 2):501-503.