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.

MeSH information

Definition | Details | More General Concepts | Related Concepts | More Specific Concepts

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 Etat Marbre Etat Marbre Status Marmoratus

Below are MeSH descriptors whose meaning is more general than "Movement Disorders".

Diseases [C]
Nervous System Diseases [C10]
Central Nervous System Diseases [C10.228]
Movement Disorders [C10.228.662]

Below are MeSH descriptors whose meaning is related to "Movement Disorders".

Below are MeSH descriptors whose meaning is more specific than "Movement Disorders".

publications

Timeline | Most Recent

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.

Bar chart showing 19 publications over 13 distinct years, with a maximum of 3 publications in 2006 and 2009

To see the data from this visualization as text, click here.

Year	Major Topic	Minor Topic	Total
1995	1	0	1
2001	0	1	1
2004	0	1	1
2006	2	1	3
2007	0	1	1
2009	2	1	3
2011	1	0	1
2013	0	1	1
2014	1	0	1
2017	0	1	1
2021	2	0	2
2023	1	0	1
2025	2	0	2

Below are the most recent publications written about "Movement Disorders" by people in Profiles.

Jones CA, Huckabee ML, Malandraki GA, Paydarfar D. Classifying neurogenic dysphagia as a movement disorder. Brain. 2025 Oct 03; 148(10):3456-3472.

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Vetkas A, Yang A, Boutet A, Cheyuo C, Santyr B, Sarica C, Davidson B, Fomenko A, Samuel N, Lang S, Sumarac S, Milosevic L, Valiante T, Hodaie M, Kalia SK, Lozano AM. One Side or Two? A Systematic Review of Deep Brain Stimulation Approaches in Movement Disorders. Mov Disord Clin Pract. 2025 Dec; 12(12):2080-2091.

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Ream MA, Lam WKK, Grosse SD, Ojodu J, Jones E, Prosser LA, Rose AM, Comeau AM, Tanksley S, Powell CM, Kemper AR. Evidence and Recommendation for Guanidinoacetate Methyltransferase Deficiency Newborn Screening. Pediatrics. 2023 08 01; 152(2).

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Lin CR, Rosendale N, Deeb W. Expanding sexual and gender minority research in movement disorders: More than awareness and acceptance. Parkinsonism Relat Disord. 2021 06; 87:162-165.

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Apetauerova D, Patel PA, Burns JD, Lerner DP. Movement Disorder Emergencies. Neurol Clin. 2021 05; 39(2):615-630.

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Deb A, Frank S, Testa CM. New symptomatic therapies for Huntington disease. Handb Clin Neurol. 2017; 144:199-207.

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Liu YB, Tewari A, Salameh J, Arystarkhova E, Hampton TG, Brashear A, Ozelius LJ, Khodakhah K, Sweadner KJ. A dystonia-like movement disorder with brain and spinal neuronal defects is caused by mutation of the mouse laminin ?1 subunit, Lamb1. Elife. 2015 Dec 24; 4.

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Tong F, Ramirez-Zamora A, Gee L, Pilitsis J. Unusual complications of deep brain stimulation. Neurosurg Rev. 2015 Apr; 38(2):245-52; discussion 252.

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Ng J, Zhen J, Meyer E, Erreger K, Li Y, Kakar N, Ahmad J, Thiele H, Kubisch C, Rider NL, Morton DH, Strauss KA, Puffenberger EG, D'Agnano D, Anikster Y, Carducci C, Hyland K, Rotstein M, Leuzzi V, Borck G, Reith ME, Kurian MA. Dopamine transporter deficiency syndrome: phenotypic spectrum from infancy to adulthood. Brain. 2014 Apr; 137(Pt 4):1107-19.

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Zacharias M, Tighe DA, Aurigemma G. A Case of LV "Pseudo" Pseudodyskinesis. Echocardiography. 2013 Oct; 30(9):1118-20.

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