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Meanings of huntington disease in английском

русский
болезнь хантингтона
португальский
coréia de huntington
испанский
mal de huntington
каталонский
síndrome de huntington
Wikidata

Rare neurodegenerative disorder of the central nervous system characterized by unwanted choreatic movements, behavioral and psychiatric disturbances and dementia.

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        Related terms
        болезнь хантингтона
        Синонимы
        Examples for "hd"
        Examples for "hd"
        1
        Conclusions: The present data suggest that CIMT is enlarged in HD patients.
        Pubmed
        2
        An HD hooked up to a Time Capsule works fine, for example.
        Wired
        3
        Conclusions: rGFR is better maintained in PD patients than in HD patients.
        Pubmed
        4
        Despite the HD programming, Voom is far from a slam-dunk for consumers.
        Wired
        5
        This scarcity is especially evident for adults and severe forms of HD.
        Pubmed
        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.
        Applied Eugenics
        2
        Huntington's Chorea, which usually appears to be a good dominant, although the last investigators (Muncey and Davenport) found some unconformable cases.
        Applied Eugenics
        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.
        Anomalies and Curiosities of Medicine
        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.
        Pubmed
        Usage of huntington disease in английском
        1
        Whether Huntington disease is responsible for the abnormally low bispectral index remains uncertain.
        Pubmed
        2
        Despite recent important discoveries, the pathogenesis of Huntington disease is still not elucidated.
        Pubmed
        3
        An expansion of a trinucleotide CAG repeat on chromosome 4 causes Huntington disease.
        Pubmed
        4
        Our data provide proof-of-principle for the potential of inducing autophagy to treat Huntington disease.
        Pubmed
        5
        Jean Fleming from the Otago School of Medicine discusses the genetic disorder Huntington Disease.
        Radio NZ
        6
        The involvement of MT 1 receptors in Alzheimer's and Huntington diseases has also been proposed.
        Pubmed
        7
        Huntington disease is one of nine inherited neurodegenerative disorders caused by a polyglutamine tract expansion.
        Pubmed
        8
        Predictive testing follows the Huntington disease protocol.
        Pubmed
        9
        These properties have shown promise in the treatment of conditions such as rheumatoid arthritis, Huntington disease, and multiple sclerosis.
        Pubmed
        10
        Teva Pharmaceutical Industries Ltd's drug, SD-809, is also in late-stage development to treat involuntary movements associated with Huntington disease.
        Reuters
        11
        Several markers closer to Huntington disease have since been isolated, but these all appear to be proximal to the defect.
        Pubmed
        12
        Appropriate nursing-care strategies depend on the early recognition of Huntington disease (HD) to prioritize a plan of care.
        Pubmed
        13
        Phosphorylation of this residue has been implicated in Huntington disease, but the mechanism by which Ser-175 phosphorylation affects transport is unclear.
        Pubmed
        14
        Huntington disease (HD) is most prevalent among populations of western European descent and isolated populations where founder effects may operate.
        Pubmed
        15
        We conclude that bilateral selective excitotoxic lesions of the posterior putamen provide an improved model of the movement disorder of Huntington disease.
        Pubmed
        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.
        Pubmed