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Meanings of huntington disease in English
Russian
болезнь хантингтона Portuguese
coréia de huntington Spanish
mal de huntington Catalan
síndrome de huntington 
Rare neurodegenerative disorder of the central nervous system characterized by unwanted choreatic movements, behavioral and psychiatric disturbances and dementia.
See moreRelated terms
Synonyms
Examples for "hd"
Examples for "hd"
1
Conclusions: The present data suggest that CIMT is enlarged in HD patients.
2
An HD hooked up to a Time Capsule works fine, for example.
3
Conclusions: rGFR is better maintained in PD patients than in HD patients.
4
Despite the HD programming, Voom is far from a slam-dunk for consumers.
5
This scarcity is especially evident for adults and severe forms of HD.
1
Such advice can be given only in the case of a few pathological characters such as color-blindness, night-blindness, or Huntington's Chorea.
2
Huntington's Chorea, which usually appears to be a good dominant, although the last investigators (Muncey and Davenport) found some unconformable cases.
3
The silly, dancing, posturing, wiry movements, and the facial distortion observed in Huntington's chorea would hardly be mistaken by a careful observer for athetosis.
1
Slight but significantly reduced levels of both lactate and citrate, however, were found in cerebrospinal fluid from patients with Huntington chorea compared to controls.
Usage of huntington disease in English
1
Whether Huntington disease is responsible for the abnormally low bispectral index remains uncertain.
2
Despite recent important discoveries, the pathogenesis of Huntington disease is still not elucidated.
3
An expansion of a trinucleotide CAG repeat on chromosome 4 causes Huntington disease.
4
Our data provide proof-of-principle for the potential of inducing autophagy to treat Huntington disease.
5
Jean Fleming from the Otago School of Medicine discusses the genetic disorder Huntington Disease.
6
The involvement of MT 1 receptors in Alzheimer's and Huntington diseases has also been proposed.
7
Huntington disease is one of nine inherited neurodegenerative disorders caused by a polyglutamine tract expansion.
8
Predictive testing follows the Huntington disease protocol.
9
These properties have shown promise in the treatment of conditions such as rheumatoid arthritis, Huntington disease, and multiple sclerosis.
10
Teva Pharmaceutical Industries Ltd's drug, SD-809, is also in late-stage development to treat involuntary movements associated with Huntington disease.
11
Several markers closer to Huntington disease have since been isolated, but these all appear to be proximal to the defect.
12
Appropriate nursing-care strategies depend on the early recognition of Huntington disease (HD) to prioritize a plan of care.
13
Phosphorylation of this residue has been implicated in Huntington disease, but the mechanism by which Ser-175 phosphorylation affects transport is unclear.
14
Huntington disease (HD) is most prevalent among populations of western European descent and isolated populations where founder effects may operate.
15
We conclude that bilateral selective excitotoxic lesions of the posterior putamen provide an improved model of the movement disorder of Huntington disease.
16
Aberrant activation of caspase-6 has recently emerged as a major contributor to the pathogeneses of neurodegenerative disorders such as Alzheimer's and Huntington disease.
Translations for huntington disease