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Rare neurodegenerative disorder of the central nervous system characterized by unwanted choreatic movements, behavioral and psychiatric disturbances and dementia.
Conclusions: The present data suggest that CIMT is enlarged in HD patients.
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An HD hooked up to a Time Capsule works fine, for example.
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Conclusions: rGFR is better maintained in PD patients than in HD patients.
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Despite the HD programming, Voom is far from a slam-dunk for consumers.
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This scarcity is especially evident for adults and severe forms of HD.
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Whether Huntingtondisease is responsible for the abnormally low bispectral index remains uncertain.
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Despite recent important discoveries, the pathogenesis of Huntingtondisease is still not elucidated.
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An expansion of a trinucleotide CAG repeat on chromosome 4 causes Huntingtondisease.
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Our data provide proof-of-principle for the potential of inducing autophagy to treat Huntingtondisease.
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Jean Fleming from the Otago School of Medicine discusses the genetic disorder HuntingtonDisease.
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Such advice can be given only in the case of a few pathological characters such as color-blindness, night-blindness, or Huntington'sChorea.
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Huntington'sChorea, which usually appears to be a good dominant, although the last investigators (Muncey and Davenport) found some unconformable cases.
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The silly, dancing, posturing, wiry movements, and the facial distortion observed in Huntington'schorea would hardly be mistaken by a careful observer for athetosis.
Usage of huntington chorea in English
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Slight but significantly reduced levels of both lactate and citrate, however, were found in cerebrospinal fluid from patients with Huntingtonchorea compared to controls.