 Movement Disorders
"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
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| MeSH Number(s) |
C10.228.662
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| Concept/Terms |
Movement Disorders- Movement Disorders
- Movement Disorder
- Movement Disorder Syndromes
- Movement Disorder Syndrome
- Dyskinesia Syndromes
- Dyskinesia Syndrome
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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 |
|---|
| 1995 | 0 | 1 | 1 | | 1997 | 1 | 0 | 1 | | 2005 | 2 | 0 | 2 | | 2006 | 1 | 0 | 1 | | 2007 | 0 | 1 | 1 | | 2008 | 1 | 0 | 1 | | 2009 | 0 | 1 | 1 | | 2010 | 1 | 0 | 1 | | 2012 | 1 | 0 | 1 | | 2013 | 2 | 2 | 4 | | 2014 | 1 | 0 | 1 | | 2015 | 1 | 0 | 1 | | 2016 | 0 | 1 | 1 | | 2017 | 4 | 0 | 4 | | 2018 | 1 | 1 | 2 | | 2019 | 0 | 3 | 3 | | 2020 | 1 | 1 | 2 | | 2021 | 2 | 0 | 2 | | 2022 | 3 | 0 | 3 | | 2023 | 3 | 0 | 3 | | 2025 | 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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Cobb LP, Shane KA, McGee PN, Nesbit C, Brennan E, Moore J, Girolami GL, Dannemiller L, Donaldson C, Boynewics K, Carey H, Chase KM, Hall A, Jones M, O'Shea RK, Zipp GP. Movement System Diagnosis: A Consensus-Based Position for Pediatric Movement Specialists. Pediatr Phys Ther. 2025 Apr 01; 37(2):257-264.
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Pan X, Alvarez AN, Ma M, Lu S, Crawford MW, Briere LC, Kanca O, Yamamoto S, Sweetser DA, Wilson JL, Napier RJ, Pruneda JN, Bellen HJ. Allelic strengths of encephalopathy-associated UBA5 variants correlate between in vivo and in vitro assays. Elife. 2023 Dec 11; 12.
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Daniels C, Greene C, Smith L, Pestana-Knight E, Demarest S, Zhang B, Benke TA, Poduri A, Olson HE. CDKL5 deficiency disorder and other infantile-onset genetic epilepsies. Dev Med Child Neurol. 2024 Apr; 66(4):456-468.
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Kawahisa-Piquini G, Bass LD, Pezzanite LM, Moorman VJ. Effect of age at training initiation on hoof morphology and lameness in juvenile American Quarter Horses. Equine Vet J. 2023 Sep; 55(5):765-776.
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Rodriguez-Contreras D, Gong S, Lebowitz JJ, Fedorov LM, Asad N, Dore TM, Phillips TJ, Ford CP, Williams JT, Neve KA. Gait Abnormalities and Aberrant D2 Receptor Expression and Signaling in Mice Carrying the Human Pathogenic Mutation DRD2I212F. Mol Pharmacol. 2023 03; 103(3):188-198.
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Goldman JG, Holden SK. Cognitive Syndromes Associated With Movement Disorders. Continuum (Minneap Minn). 2022 06 01; 28(3):726-749.
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Petkova SP, Adhikari A, Berg EL, Fenton TA, Duis J, Silverman JL. Gait as a quantitative translational outcome measure in Angelman syndrome. Autism Res. 2022 05; 15(5):821-833.
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Damron L, Bayram E, McGehrin K, Reynolds J, Hess R, Coughlin DG, Litvan I. Physician-Assisted Dying: Access and Utilization in Patients with Movement Disorders. Mov Disord. 2022 04; 37(4):694-698.
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Walther S, Vladimirova I, Alexaki D, Sch?ppi L, Damme KSF, Mittal VA, Shankman SA, Stegmayer K. Low physical activity is associated with two hypokinetic motor abnormalities in psychosis. J Psychiatr Res. 2022 02; 146:258-263.
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Benke TA, Park K, Krey I, Camp CR, Song R, Ramsey AJ, Yuan H, Traynelis SF, Lemke J. Clinical and therapeutic significance of genetic variation in the GRIN gene family encoding NMDARs. Neuropharmacology. 2021 11 01; 199:108805.
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