"Basal Ganglia Diseases" 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.
Diseases of the BASAL GANGLIA including the PUTAMEN; GLOBUS PALLIDUS; claustrum; AMYGDALA; and CAUDATE NUCLEUS. DYSKINESIAS (most notably involuntary movements and alterations of the rate of movement) represent the primary clinical manifestations of these disorders. Common etiologies include CEREBROVASCULAR DISORDERS; NEURODEGENERATIVE DISEASES; and CRANIOCEREBRAL TRAUMA.
| Descriptor ID |
D001480
|
| MeSH Number(s) |
C10.228.140.079
|
| Concept/Terms |
Basal Ganglia Diseases- Basal Ganglia Diseases
- Basal Ganglia Disease
- Basal Ganglia Disorders
- Basal Ganglia Disorder
|
Below are MeSH descriptors whose meaning is more general than "Basal Ganglia Diseases".
Below are MeSH descriptors whose meaning is more specific than "Basal Ganglia Diseases".
This graph shows the total number of publications written about "Basal Ganglia Diseases" by people in this website by year, and whether "Basal Ganglia Diseases" 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 |
|---|
| 1994 | 0 | 1 | 1 |
| 1995 | 1 | 0 | 1 |
| 1996 | 1 | 1 | 2 |
| 1997 | 1 | 0 | 1 |
| 1998 | 1 | 0 | 1 |
| 1999 | 0 | 1 | 1 |
| 2000 | 0 | 1 | 1 |
| 2001 | 1 | 0 | 1 |
| 2002 | 1 | 0 | 1 |
| 2003 | 1 | 0 | 1 |
| 2007 | 2 | 0 | 2 |
| 2011 | 0 | 1 | 1 |
| 2013 | 1 | 0 | 1 |
| 2014 | 0 | 1 | 1 |
| 2016 | 1 | 0 | 1 |
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Below are the most recent publications written about "Basal Ganglia Diseases" by people in Profiles.
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Ifngr1 and Stat1 mediated canonical Ifn-? signaling drives nigrostriatal degeneration. Neurobiol Dis. 2018 02; 110:133-141.
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Serum Ferritin, Weight Gain, Disruptive Behavior, and Extrapyramidal Symptoms in Risperidone-Treated Youth. J Child Adolesc Psychopharmacol. 2016 06; 26(5):471-7.
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Fulminant corticobasal degeneration: Agrypnia excitata in corticobasal syndrome. Neurology. 2016 Mar 22; 86(12):1164-6.
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Basal ganglia circuits for reward value-guided behavior. Annu Rev Neurosci. 2014; 37:289-306.
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Exome sequencing in familial corticobasal degeneration. Parkinsonism Relat Disord. 2013 Nov; 19(11):1049-52.
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Symmetrical corticobasal syndrome caused by a novel C.314dup progranulin mutation. J Mol Neurosci. 2011 Nov; 45(3):354-8.
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Use of a minimally invasive tubular retraction system for deep-seated tumors in pediatric patients. J Neurosurg Pediatr. 2011 May; 7(5):516-21.
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Clinical and molecular phenotype of Aicardi-Goutieres syndrome. Am J Hum Genet. 2007 Oct; 81(4):713-25.
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Ethnic origin and extrapyramidal signs in an Argentinean spinocerebellar ataxia type 10 family. Neurology. 2007 Jul 10; 69(2):216-8.
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Evolution of basal ganglia surgery for movement disorders. Stereotact Funct Neurosurg. 2006; 84(4):131-5.