 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
Lingual-Facial-Buccal Dyskinesia- Lingual-Facial-Buccal Dyskinesia
- Dyskinesia, Lingual-Facial-Buccal
- Dyskinesias, Lingual-Facial-Buccal
- Lingual Facial Buccal Dyskinesia
- Lingual-Facial-Buccal Dyskinesias
- Tardive Dyskinesia
- Dyskinesia, Tardive
- Dyskinesias, Tardive
- Tardive Dyskinesias
- Oral-facial Dyskinesia
- Dyskinesia, Oral-facial
- Dyskinesias, Oral-facial
- Oral facial Dyskinesia
- Oral-facial Dyskinesias
- Tardive Oral Dyskinesia
- Tardive Oral Dyskinesias
- Linguofacial Dyskinesia
- Dyskinesia, Linguofacial
- Dyskinesias, Linguofacial
- Linguofacial Dyskinesias
- Orofacial Dyskinesia
- Dyskinesia, Orofacial
- Dyskinesias, Orofacial
- Orofacial Dyskinesias
- Tardive Dystonia
- Dystonia, Tardive
- Dystonias, Tardive
- Tardive Dystonias
Oral Dyskinesia- Oral Dyskinesia
- Dyskinesia, Oral
- Dyskinesias, Oral
- Oral Dyskinesias
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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 |
|---|
| 1990 | 3 | 0 | 3 | | 1994 | 0 | 2 | 2 | | 1998 | 1 | 2 | 3 | | 2001 | 0 | 1 | 1 | | 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 |
To return to the timeline, click here.
Below are the most recent publications written about "Movement Disorders" by people in Profiles.
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Mochel F, Rastetter A, Ceulemans B, Platzer K, Yang S, Shinde DN, Helbig KL, Lopergolo D, Mari F, Renieri A, Benetti E, Canitano R, Waisfisz Q, Plomp AS, Huisman SA, Wilson GN, Cathey SS, Louie RJ, Gaudio DD, Waggoner D, Kacker S, Nugent KM, Roeder ER, Bruel AL, Thevenon J, Ehmke N, Horn D, Holtgrewe M, Kaiser FJ, Kamphausen SB, Abou Jamra R, Weckhuysen S, Dalle C, Depienne C. 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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Polster SP, Dougherty MC, Zeineddine HA, Lee SK, Frim D. 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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Drobyshevsky A, Jiang R, Lin L, Derrick M, Luo K, Back SA, Tan S. Unmyelinated axon loss with postnatal hypertonia after fetal hypoxia. Ann Neurol. 2014 Apr; 75(4):533-41.
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Radman N, Cacioppo S, Spierer L, Schmidlin E, Mayer E, Annoni JM. Posterior SMA Syndrome following subcortical stroke: contralateral akinesia reversed by visual feedback. Neuropsychologia. 2013 Nov; 51(13):2605-10.
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Bögershausen N, Shahrzad N, Chong JX, von Kleist-Retzow JC, Stanga D, Li Y, Bernier FP, Loucks CM, Wirth R, Puffenberger EG, Hegele RA, Schreml J, Lapointe G, Keupp K, Brett CL, Anderson R, Hahn A, Innes AM, Suchowersky O, Mets MB, Nürnberg G, McLeod DR, Thiele H, Waggoner D, Altmüller J, Boycott KM, Schoser B, Nürnberg P, Ober C, Heller R, Parboosingh JS, Wollnik B, Sacher M, Lamont RE. 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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Ehrenpreis ED, Deepak P, Sifuentes H, Devi R, Du H, Leikin JB. 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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Drobyshevsky A, Luo K, Derrick M, Yu L, Du H, Prasad PV, Vasquez-Vivar J, Batinic-Haberle I, Tan S. 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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Gong P, Roseman J, Fernandez CG, Vetrivel KS, Bindokas VP, Zitzow LA, Kar S, Parent AT, Thinakaran G. 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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Pandey P, Bell-Stephens T, Steinberg GK. Patients with moyamoya disease presenting with movement disorder. J Neurosurg Pediatr. 2010 Dec; 6(6):559-66.
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Tate MC, Kim CY, Chang EF, Polley MY, Berger MS. Assessment of morbidity following resection of cingulate gyrus gliomas. Clinical article. J Neurosurg. 2011 Mar; 114(3):640-7.
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