Blood Platelet Disorders
"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
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MeSH Number(s) |
C15.378.140
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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
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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.
To see the data from this visualization as text, click here.
Year | Major Topic | Minor Topic | Total |
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2010 | 1 | 0 | 1 | 2014 | 0 | 1 | 1 | 2021 | 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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Homan CC, King-Smith SL, Lawrence DM, Arts P, Feng J, Andrews J, Armstrong M, Ha T, Dobbins J, Drazer MW, Yu K, Bödör C, Cantor A, Cazzola M, Degelman E, DiNardo CD, Duployez N, Favier R, Fröhling S, Fitzgibbon J, Klco JM, Krämer A, Kurokawa M, Lee J, Malcovati L, Morgan NV, Natsoulis G, Owen C, Patel KP, Preudhomme C, Raslova H, Rienhoff H, Ripperger T, Schulte R, Tawana K, Velloso E, Yan B, Liu P, Godley LA, Schreiber AW, Hahn CN, Scott HS, Brown AL. 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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El Husseini N, Kaskar O, Goldstein LB. Chronic kidney disease and stroke. Adv Chronic Kidney Dis. 2014 Nov; 21(6):500-8.
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Churpek JE, Garcia JS, Madzo J, Jackson SA, Onel K, Godley LA. Identification and molecular characterization of a novel 3′ mutation in RUNX1 in a family with familial platelet disorder. Leuk Lymphoma. 2010 Oct; 51(10):1931-5.
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Miller JL. Glycoprotein analysis for the diagnostic evaluation of platelet disorders. Semin Thromb Hemost. 2009 Mar; 35(2):224-32.
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Sweet DL, Golomb HM. Correction of platelet defect after splenectomy in hairy cell leukemia. JAMA. 1979 Apr 20; 241(16):1684.
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Caprini JA, Kurtides ES, Dorsey JM. Coagulation changes in acutely bleeding patients. Arch Surg. 1972 Apr; 104(4):559-64.
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Rowley JD, Blaisdell RK. Karyotype of treated thrombocythemia. Lancet. 1966 Jul 09; 2(7454):104-5.
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