"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.
To see the data from this visualization as text,
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| Year | Major Topic | Minor Topic | Total |
|---|
| 1998 | 1 | 0 | 1 |
| 2000 | 1 | 0 | 1 |
| 2002 | 1 | 0 | 1 |
| 2004 | 1 | 0 | 1 |
| 2010 | 1 | 0 | 1 |
| 2014 | 1 | 0 | 1 |
| 2016 | 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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Erythropoietin and thrombopoietin mimetics: Natural alternatives to erythrocyte and platelet disorders. Crit Rev Oncol Hematol. 2016 Dec; 108:175-186.
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Activating mutations in STIM1 and ORAI1 cause overlapping syndromes of tubular myopathy and congenital miosis. Proc Natl Acad Sci U S A. 2014 Mar 18; 111(11):4197-202.
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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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Congenital platelet disorders. Hematol Oncol Clin North Am. 2007 Aug; 21(4):663-84, vi.
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For low platelets, how low is dangerous? Cleve Clin J Med. 2004 Apr; 71(4):277-8.
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Human platelet Galphaq deficiency is associated with decreased Galphaq gene expression in platelets but not neutrophils. Thromb Haemost. 2002 Jan; 87(1):129-33.
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Platelets. Lancet. 2000 Apr 29; 355(9214):1531-9.
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PFA-100 system: a new method for assessment of platelet dysfunction. Semin Thromb Hemost. 1998; 24(2):195-202.
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The clinical importance of acquired abnormalities of platelet function. N Engl J Med. 1991 Jan 03; 324(1):27-39.