"Movement 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.
Syndromes which feature DYSKINESIAS as a cardinal manifestation of the disease process. Included in this category are degenerative, hereditary, post-infectious, medication-induced, post-inflammatory, and post-traumatic conditions.
Descriptor ID |
D009069
|
MeSH Number(s) |
C10.228.662
|
Concept/Terms |
Movement Disorders- Movement Disorders
- Movement Disorder
- Movement Disorder Syndromes
- Movement Disorder Syndrome
- Dyskinesia Syndromes
- Dyskinesia Syndrome
|
Below are MeSH descriptors whose meaning is more general than "Movement Disorders".
Below are MeSH descriptors whose meaning is more specific than "Movement Disorders".
This graph shows the total number of publications written about "Movement Disorders" by people in this website by year, and whether "Movement 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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1994 | 0 | 2 | 2 |
1998 | 1 | 2 | 3 |
2001 | 1 | 1 | 2 |
2003 | 1 | 0 | 1 |
2005 | 0 | 1 | 1 |
2006 | 2 | 1 | 3 |
2007 | 2 | 1 | 3 |
2008 | 0 | 2 | 2 |
2009 | 3 | 0 | 3 |
2010 | 2 | 1 | 3 |
2011 | 1 | 0 | 1 |
2012 | 1 | 0 | 1 |
2013 | 1 | 1 | 2 |
2014 | 1 | 0 | 1 |
2018 | 0 | 1 | 1 |
2020 | 1 | 0 | 1 |
2022 | 1 | 0 | 1 |
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Below are the most recent publications written about "Movement Disorders" by people in Profiles.
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Using Downgaze Palsy Progression Rate to Model Survival in Progressive Supranuclear Palsy-Richardson Syndrome. Mov Disord. 2023 02; 38(2):304-312.
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Variants in the SK2 channel gene (KCNN2) lead to dominant neurodevelopmental movement disorders. Brain. 2020 12 01; 143(12):3564-3573.
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A Report of 2 Cases of Brainstem Hemorrhage After Suboccipital Craniectomy for Chiari Decompression. Oper Neurosurg (Hagerstown). 2018 05 01; 14(5):598.
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Unmyelinated axon loss with postnatal hypertonia after fetal hypoxia. Ann Neurol. 2014 Apr; 75(4):533-41.
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Posterior SMA Syndrome following subcortical stroke: contralateral akinesia reversed by visual feedback. Neuropsychologia. 2013 Nov; 51(13):2605-10.
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Recessive TRAPPC11 mutations cause a disease spectrum of limb girdle muscular dystrophy and myopathy with movement disorder and intellectual disability. Am J Hum Genet. 2013 Jul 11; 93(1):181-90.
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The metoclopramide black box warning for tardive dyskinesia: effect on clinical practice, adverse event reporting, and prescription drug lawsuits. Am J Gastroenterol. 2013 Jun; 108(6):866-72.
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Motor deficits are triggered by reperfusion-reoxygenation injury as diagnosed by MRI and by a mechanism involving oxidants. J Neurosci. 2012 Apr 18; 32(16):5500-9.
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Transgenic neuronal overexpression reveals that stringently regulated p23 expression is critical for coordinated movement in mice. Mol Neurodegener. 2011 Dec 28; 6:87.
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Patients with moyamoya disease presenting with movement disorder. J Neurosurg Pediatr. 2010 Dec; 6(6):559-66.