"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 |
|---|
| 1996 | 1 | 0 | 1 |
| 1997 | 2 | 0 | 2 |
| 1998 | 1 | 2 | 3 |
| 2000 | 1 | 2 | 3 |
| 2001 | 2 | 2 | 4 |
| 2002 | 1 | 1 | 2 |
| 2003 | 4 | 1 | 5 |
| 2004 | 3 | 1 | 4 |
| 2005 | 1 | 1 | 2 |
| 2006 | 3 | 1 | 4 |
| 2007 | 1 | 1 | 2 |
| 2008 | 3 | 1 | 4 |
| 2009 | 6 | 0 | 6 |
| 2010 | 8 | 0 | 8 |
| 2011 | 7 | 1 | 8 |
| 2012 | 7 | 0 | 7 |
| 2013 | 15 | 1 | 16 |
| 2014 | 11 | 2 | 13 |
| 2015 | 7 | 0 | 7 |
| 2016 | 5 | 0 | 5 |
| 2017 | 7 | 0 | 7 |
| 2018 | 2 | 1 | 3 |
| 2019 | 6 | 0 | 6 |
| 2020 | 2 | 1 | 3 |
| 2021 | 10 | 0 | 10 |
| 2022 | 4 | 0 | 4 |
| 2023 | 8 | 0 | 8 |
| 2024 | 3 | 0 | 3 |
| 2025 | 5 | 0 | 5 |
| 2026 | 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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Opisthotonus: Revisiting a classic movement disorder. J Neurol Sci. 2026 Mar 15; 482:125782.
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Genetic variants in ESRRG are associated with a dominant non-progressive congenital movement disorder with ataxia. Am J Hum Genet. 2025 Dec 04; 112(12):2961-2972.
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Longitudinal Characterization of Males With X-Linked Creatine Transporter Deficiency: Final Results of a Multiyear Observational Study. Pediatr Neurol. 2026 Feb; 175:8-18.
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Surgical Complications of Deep Brain Stimulation in Children Across Targets and Indications: Multicenter Analysis of the CHILD-DBS Registry. Neurology. 2025 Nov 11; 105(9):e214201.
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Real-World Experiences with VMAT2 Inhibitors in Pediatric Hyperkinetic Movement Disorders. Tremor Other Hyperkinet Mov (N Y). 2025; 15:26.
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The social deprivation index and deep brain stimulation: A cohort study. Clin Neurol Neurosurg. 2025 May; 252:108860.
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Bi-allelic ACBD6 variants lead to a neurodevelopmental syndrome with progressive and complex movement disorders. Brain. 2024 04 04; 147(4):1436-1456.
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An Evidence-Based Update on Anticholinergic Use for Drug-Induced Movement Disorders. CNS Drugs. 2024 04; 38(4):239-254.
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Current opinions and practices in post-stroke movement disorders: Survey of movement disorders society members. J Neurol Sci. 2024 03 15; 458:122925.
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Allelic strengths of encephalopathy-associated UBA5 variants correlate between in vivo and in vitro assays. Elife. 2023 12 11; 12.