"Hyperkinesis" 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.
Excessive movement of muscles of the body as a whole, which may be associated with organic or psychological disorders.
| Descriptor ID |
D006948
|
| MeSH Number(s) |
C10.597.350.350 C23.888.592.350.350
|
| Concept/Terms |
Hyperkinesis- Hyperkinesis
- Hyperkinesia
- Hyperkinetic Movements
- Hyperkinetic Movement
- Movement, Hyperkinetic
- Movements, Hyperkinetic
- Hyperactivity, Motor
- Motor Hyperactivity
Hyperkinesia, Generalized- Hyperkinesia, Generalized
- Generalized Hyperkinesia
- Generalized Hyperkinesias
- Hyperkinesias, Generalized
|
Below are MeSH descriptors whose meaning is more general than "Hyperkinesis".
Below are MeSH descriptors whose meaning is more specific than "Hyperkinesis".
This graph shows the total number of publications written about "Hyperkinesis" by people in this website by year, and whether "Hyperkinesis" 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 |
|---|
| 2000 | 1 | 0 | 1 |
| 2002 | 0 | 2 | 2 |
| 2003 | 1 | 0 | 1 |
| 2006 | 2 | 1 | 3 |
| 2007 | 1 | 0 | 1 |
| 2009 | 1 | 0 | 1 |
| 2010 | 0 | 1 | 1 |
| 2011 | 1 | 0 | 1 |
| 2012 | 1 | 2 | 3 |
| 2013 | 0 | 2 | 2 |
| 2016 | 1 | 0 | 1 |
| 2023 | 1 | 0 | 1 |
| 2024 | 1 | 0 | 1 |
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Below are the most recent publications written about "Hyperkinesis" by people in Profiles.
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Hyperkinetic Movement Disorder Caused by the Recurrent c.892C>T NACC1 Variant. Mov Disord Clin Pract. 2024 Jun; 11(6):708-715.
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Paroxysmal Sympathetic Hyperactivity: Development of a Pediatric Clinical Practice Guideline. Hosp Pediatr. 2023 12 01; 13(12):e402-e410.
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Dopamine depleters in the treatment of hyperkinetic movement disorders. Expert Opin Pharmacother. 2016 Dec; 17(18):2461-2470.
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GAD1 gene polymorphisms are associated with hyperactivity in Attention-Deficit/Hyperactivity Disorder. Am J Med Genet B Neuropsychiatr Genet. 2016 12; 171(8):1099-1104.
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SHANK3 overexpression causes manic-like behaviour with unique pharmacogenetic properties. Nature. 2013 Nov 07; 503(7474):72-7.
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Unusual case of paroxysmal sympathetic hyperactivity in a patient with leukemia. Clin Neurophysiol. 2014 May; 125(5):1069-71.
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Analysis of CYP2D6 genotype and response to tetrabenazine. Mov Disord. 2013 Feb; 28(2):210-5.
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Hoarding in Children With ADHD. J Atten Disord. 2016 07; 20(7):617-26.
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Synergism between a serotonin 5-HT2A receptor (5-HT2AR) antagonist and 5-HT2CR agonist suggests new pharmacotherapeutics for cocaine addiction. ACS Chem Neurosci. 2013 Jan 16; 4(1):110-21.
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Head bobber: an insertional mutation causes inner ear defects, hyperactive circling, and deafness. J Assoc Res Otolaryngol. 2012 Jun; 13(3):335-49.