Term Gallery logo

Significados de huntington's disease em inglês

português
doença de huntington

Hereditary disease; develops in adulthood and ends in dementia.

doença de huntington
Sinônimos
Examples for "Huntington's chorea"
Examples for "Huntington's chorea"
1
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.
Anomalies and Curiosities of Medicine
2
Such advice can be given only in the case of a few pathological characters such as color-blindness, night-blindness, or Huntington's Chorea.
Applied Eugenics
3
Huntington's Chorea, which usually appears to be a good dominant, although the last investigators (Muncey and Davenport) found some unconformable cases.
Applied Eugenics
Uso de huntington's disease em inglês
1
We conclude that quantitative assessment of chorea is feasible in Huntington's disease.
Pubmed
2
Chorea is commonly assessed by subitems of the Unified- Huntington's Disease Rating Scale.
Pubmed
3
She is currently involved in two areas of research; Huntington's disease and concussion.
Radio NZ
4
We compared the extent of editing in controls and cases with Huntington's disease.
Pubmed
5
Furthermore, gut dysbiosis was recently reported in Huntington's disease transgenic mice.
Pubmed
6
Background: Postural deficits in Huntington's disease are linked to functional impairment.
Pubmed
7
No other drug tested in Huntington's disease has shown this effect.
Pubmed
8
Read more about the impact of Huntington's disease on The Wireless
Radio NZ
9
A preponderance of maternal transmission was noted in late-onset Huntington's disease.
Pubmed
10
Proteins with expanded polyglutamine domains cause eight inherited neurodegenerative diseases including Huntington's disease.
Pubmed
11
Eighty-two percent were in favour of the principle of predictive testing for Huntington's disease.
Pubmed
12
Overall, our findings suggest an altered gut microbiome in Huntington's disease gene expansion carriers.
Pubmed
13
In Huntington's disease, involuntary choreatic movements are one of the hallmarks of motor dysfunction.
Pubmed
14
The clinical features resembled those of mid-life onset Huntington's disease but progressed more slowly.
Pubmed
15
There were no group differences on the Unified Huntington's Disease Rating total motor score.
Pubmed
16
Approximately 25% of persons affected by Huntington's disease exhibit late onset.
Pubmed
Translations for huntington's disease