Search Results - "Skitt, Zara"

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  1. 1

    A feasibility investigation of mindfulness-based cognitive therapy for people with Huntington's disease by Eccles, Fiona J R, Craufurd, David, Smith, Alistair, Davies, Rhys, Glenny, Kristian, Homberger, Max, Peeren, Siofra, Rogers, Dawn, Rose, Leona, Skitt, Zara, Theed, Rachael, Simpson, Jane

    Published in Pilot and feasibility studies (24-06-2020)
    “…Huntington's disease (HD) is an inherited neurodegenerative condition which affects movement, coordination and cognitive functioning. Psychological…”
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    Journal Article
  2. 2

    M16 A pilot evaluation of mindfulness-based cognitive therapy for people with huntington’s disease by Simpson, Jane, Craufurd, David, Smith, Alistair, Eccles, Fiona, Peeren, Siofra, Rogers, Dawn, Skitt, Zara, Theed, Rachael

    “…BackgroundMany people with the Huntington’s disease (HD) gene, both pre-manifest and manifest, experience low mood, anxiety and other psychological…”
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    Journal Article
  3. 3
  4. 4

    Experiences of Mindfulness-Based Cognitive Therapy for Premanifest Huntington's Disease by Eccles, Fiona J R, Craufurd, David, Smith, Alistair, Davies, Rhys, Glenny, Kristian, Homberger, Max, Rose, Leona, Theed, Rachael, Peeren, Siofra, Rogers, Dawn, Skitt, Zara, Zarotti, Nicolò, Simpson, Jane

    Published in Journal of Huntington's disease (01-01-2021)
    “…Psychological difficulties such as anxiety, depression, and irritability are common in Huntington's disease, even for premanifest individuals. However, very…”
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    Journal Article
  5. 5

    Anxious, hypoactive phenotype combined with motor deficits in Gtf2ird1 null mouse model relevant to Williams syndrome by Schneider, Tomasz, Skitt, Zara, Liu, Yiwen, Deacon, Robert M.J., Flint, Jonathan, Karmiloff-Smith, Annette, Rawlins, J. Nick P., Tassabehji, May

    Published in Behavioural brain research (01-08-2012)
    “…► A role for GTF2IRD1 in motoric and anxiety-related phenotypes seen in Williams–Beuren syndrome. ► Gtf2ird1 null mice show decreased spontaneous and circadian…”
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    Journal Article
  6. 6

    Investigation of the behavioural phenotype of a mouse model of Williams-Beuren Syndrome (Gtf2ird1) by Skitt, Zara

    Published 01-01-2013
    “…Williams-beuren syndrome (WBS) is caused by a deletion of ~25 genes and is characterised by cardiovascular dysfunction, an uneven cognitive profile and a…”
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    Dissertation