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期刊名:Journal of huntingtons disease

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ISSN:1879-6397

e-ISSN:1879-6400

IF/分区:2.7/Q3

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共收录本刊相关文章索引486
Clinical Trial Case Reports Meta-Analysis RCT Review Systematic Review
Classical Article Case Reports Clinical Study Clinical Trial Clinical Trial Protocol Comment Comparative Study Editorial Guideline Letter Meta-Analysis Multicenter Study Observational Study Randomized Controlled Trial Review Systematic Review
Marleen R van Walsem,Emilie I Howe,Jan C Frich et al. Marleen R van Walsem et al.
Background: Assistive technology for cognition (ATC) can be defined as external devices aimed at supporting cognitive function. Studies in neurological populations suggest that use of ATC is a promising strategy to amelio...
Stephen J Sawiak,Nigel I Wood,A Jennifer Morton Stephen J Sawiak
Background: Huntington's disease (HD) is caused by an unstable polyglutamine (CAG) repeat in the HD gene, whereby a CAG repeat length greater than ∼36 leads to the disease. In HD patients, longer repeats correlate with m...
Amit Kumar,Rajiv R Ratan Amit Kumar
Redox homeostasis is crucial for proper cellular functions, including receptor tyrosine kinase signaling, protein folding, and xenobiotic detoxification. Under basal conditions, there is a balance between oxidants and antioxidants. This bal...
Fabian Kreilaus,Adena S Spiro,Anthony J Hannan et al. Fabian Kreilaus et al.
Background: Huntington's disease (HD) is a progressive neurodegenerative disease with no effective treatment or cure. Environmental enrichment has been used to slow processes leading to ageing and neurodegenerative diseas...
Adelaide Tousley,Kimberly B Kegel-Gleason Adelaide Tousley
Induced pluripotent stem cells (iPSCs) derived from controls and patients can act as a starting point for in vitro differentiation into human brain cells for discovery of novel targets and treatments for human disease without the same ethic...
Jan C Frich,Daniela Rae,Richard Roxburgh et al. Jan C Frich et al.
Background: Little is known about the organization of clinical services for Huntington's disease (HD). Objective: To describe how healt...
Kelly L Andrzejewski,Ariel V Dowling,David Stamler et al. Kelly L Andrzejewski et al.
Background: The Unified Huntington's Disease Rating Scale (UHDRS) is the principal means of assessing motor impairment in Huntington disease but is subjective and generally limited to in-clinic assessments. ...
Petr Vodicka,Kathryn Chase,Maria Iuliano et al. Petr Vodicka et al.
Background: Reducing mutant huntingtin (mHTT) in neurons may be a therapy for Huntington's disease (HD). Elevating NUB1 protein reduced mHTT levels in cell and fly models of HD through a proteasome dependent mechanism. ...
Emma Yhnell,Stephen B Dunnett,Simon P Brooks Emma Yhnell
Background: Huntington's disease (HD) is a rare, incurable neurodegenerative disorder caused by a CAG trinucleotide expansion with the first exon of the huntingtin gene. Numerous knock-in mouse models are currently availa...
Anna A M Hubers,Annette Hamming,Erik J Giltay et al. Anna A M Hubers et al.
Background: Huntington's disease (HD) mutation carriers are at increased risk of suicidal ideation, suicide attempts, and completed suicide. However, research is lacking on coping strategies and treatment options that can...