 Ataxia
"Ataxia" 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.
Impairment of the ability to perform smoothly coordinated voluntary movements. This condition may affect the limbs, trunk, eyes, pharynx, larynx, and other structures. Ataxia may result from impaired sensory or motor function. Sensory ataxia may result from posterior column injury or PERIPHERAL NERVE DISEASES. Motor ataxia may be associated with CEREBELLAR DISEASES; CEREBRAL CORTEX diseases; THALAMIC DISEASES; BASAL GANGLIA DISEASES; injury to the RED NUCLEUS; and other conditions.
| Descriptor ID |
D001259
|
| MeSH Number(s) |
C10.597.350.090 C23.888.592.350.090
|
| Concept/Terms |
Ataxia- Ataxia
- Ataxias
- Coordination Impairment
- Coordination Impairments
- Impairment, Coordination
- Impairments, Coordination
- Dyssynergia
- Ataxy
Ataxia, Motor- Ataxia, Motor
- Ataxias, Motor
- Motor Ataxia
- Motor Ataxias
Tremor, Rubral- Tremor, Rubral
- Rubral Tremor
- Rubral Tremors
- Tremors, Rubral
Ataxia, Truncal- Ataxia, Truncal
- Ataxias, Truncal
- Truncal Ataxia
- Truncal Ataxias
Dyscoordination- Dyscoordination
- Lack of Coordination
- Coordination Lack
- Incoordination
- Incoordinations
Ataxia, Appendicular- Ataxia, Appendicular
- Appendicular Ataxia
- Appendicular Ataxias
- Ataxias, Appendicular
- Ataxia, Limb
- Ataxias, Limb
- Limb Ataxia
- Limb Ataxias
Ataxia, Sensory- Ataxia, Sensory
- Ataxias, Sensory
- Sensory Ataxia
- Sensory Ataxias
|
Below are MeSH descriptors whose meaning is more general than "Ataxia".
Below are MeSH descriptors whose meaning is more specific than "Ataxia".
This graph shows the total number of publications written about "Ataxia" by people in this website by year, and whether "Ataxia" 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 |
|---|
| 2010 | 2 | 0 | 2 | | 2012 | 2 | 0 | 2 | | 2013 | 0 | 1 | 1 | | 2017 | 1 | 0 | 1 | | 2020 | 0 | 1 | 1 | | 2022 | 2 | 0 | 2 |
To return to the timeline, click here.
Below are the most recent publications written about "Ataxia" by people in Profiles.
-
Amadori E, Pellino G, Bansal L, Mazzone S, M?ller RS, Rubboli G, Striano P, Russo A. Answer to: Genetic paroxysmal neurological disorders featuring episodic ataxia and epilepsy (Amadori E et al., 2022). EJMG-D-22-00384. Eur J Med Genet. 2022 12; 65(12):104634.
-
Amadori E, Pellino G, Bansal L, Mazzone S, M?ller RS, Rubboli G, Striano P, Russo A. Genetic paroxysmal neurological disorders featuring episodic ataxia and epilepsy. Eur J Med Genet. 2022 Apr; 65(4):104450.
-
Mao D, Reuter CM, Ruzhnikov MRZ, Beck AE, Farrow EG, Emrick LT, Rosenfeld JA, Mackenzie KM, Robak L, Wheeler MT, Burrage LC, Jain M, Liu P, Calame D, K?ry S, Sillesen M, Schmitz-Abe K, Tonduti D, Spaccini L, Iascone M, Genetti CA, Koenig MK, Graf M, Tran A, Alejandro M, Lee BH, Thiffault I, Agrawal PB, Bernstein JA, Bellen HJ, Chao HT. De novo EIF2AK1 and EIF2AK2 Variants Are Associated with Developmental Delay, Leukoencephalopathy, and Neurologic Decompensation. Am J Hum Genet. 2020 04 02; 106(4):570-583.
-
Tucker MH, Holmes J, Harley S, Garcia MR, Custodio H. Case 1: Fever and Ataxia in a Toddler with Pica. Pediatr Rev. 2017 Sep; 38(9):435-436.
-
Dinwiddie DL, Smith LD, Miller NA, Atherton AM, Farrow EG, Strenk ME, Soden SE, Saunders CJ, Kingsmore SF. Diagnosis of mitochondrial disorders by concomitant next-generation sequencing of the exome and mitochondrial genome. Genomics. 2013 Sep; 102(3):148-56.
-
Bayat V, Thiffault I, Jaiswal M, T?treault M, Donti T, Sasarman F, Bernard G, Demers-Lamarche J, Dicaire MJ, Mathieu J, Vanasse M, Bouchard JP, Rioux MF, Lourenco CM, Li Z, Haueter C, Shoubridge EA, Graham BH, Brais B, Bellen HJ. Mutations in the mitochondrial methionyl-tRNA synthetase cause a neurodegenerative phenotype in flies and a recessive ataxia (ARSAL) in humans. PLoS Biol. 2012; 10(3):e1001288.
-
T?treault M, Putorti ML, Thiffault I, Sylvain M, Venderver A, Schiffmann R, Brais B, Bernard G. TACH leukodystrophy: locus refinement to chromosome 10q22.3-23.1. Can J Neurol Sci. 2012 Jan; 39(1):122-3.
-
Valdmanis PN, Dupr? N, Lachance M, Stochmanski SJ, Belzil VV, Dion PA, Thiffault I, Brais B, Weston L, Saint-Amant L, Samuels ME, Rouleau GA. A mutation in the RNF170 gene causes autosomal dominant sensory ataxia. Brain. 2011 Feb; 134(Pt 2):602-7.
-
Bernard G, Thiffault I, Tetreault M, Putorti ML, Bouchard I, Sylvain M, Melan?on S, Laframboise R, Langevin P, Bouchard JP, Vanasse M, Vanderver A, S?bire G, Brais B. Tremor-ataxia with central hypomyelination (TACH) leukodystrophy maps to chromosome 10q22.3-10q23.31. Neurogenetics. 2010 Oct; 11(4):457-64.
-
Magdaleno S, Keshvara L, Curran T. Rescue of ataxia and preplate splitting by ectopic expression of Reelin in reeler mice. Neuron. 2002 Feb 14; 33(4):573-86.
|
People  People who have written about this concept. _
Similar Concepts
People who have written about this concept.
_
Top Journals
Top journals in which articles about this concept have been published.
|