首页 文献索引 SCI期刊 AI助手
期刊目录筛选

期刊名:Journal of huntingtons disease

缩写:

ISSN:1879-6397

e-ISSN:1879-6400

IF/分区:2.7/Q3

文章目录 更多期刊信息

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
Raheleh Heidari,Véronique Monnier,Elodie Martin et al. Raheleh Heidari et al.
Background: Huntington's disease (HD) is a Polyglutamine disease caused by the presence of CAG repeats in the first exon of Huntingtin (Htt), a large protein with multiple functions. In addition to neurodegeneration of sp...
Matthew Mort,Francesca A Carlisle,Adrian J Waite et al. Matthew Mort et al.
Background: A CAG repeat expansion in HTT has been known to cause Huntington's disease for over 20 years. The genomic sequence of the 67 exon HTT is clear but few reports have detailed alternative splicing or alternative ...
Jessica J Steventon,David J Harrison,Rebecca C Trueman et al. Jessica J Steventon et al.
Background: Environmental enrichment has been shown to improve symptoms and reduce neuropathology in mouse models of Huntington's disease (HD); however results are limited to ex vivo techniques with associated shortcoming...
Mayke Oosterloo,Martine J Van Belzen,Emilia K Bijlsma et al. Mayke Oosterloo et al.
Background and objective: Huntington's disease (HD) is a neurodegenerative disease associated with a CAG repeat expansion in the Huntingtin (HTT) gene. A trinucleotide size between 27 and 35 is considered 'intermediate' a...
Joakim Tedroff,Susanna Waters,Roger A Barker et al. Joakim Tedroff et al.
Background: Huntington's disease (HD) is an autosomal dominant neurodegenerative disorder leading to progressive motor, cognitive and functional decline. Antidopaminergic medications (ADMs) are frequently used to treat ch...
Eleftheria Vaportzis,Nellie Georgiou-Karistianis,Andrew Churchyard et al. Eleftheria Vaportzis et al.
Background: Past research has found cancellation tasks to be reliable markers of cognitive decline in Huntington's disease (HD). Objective: ...
Gelareh Mazarei,Blair R Leavitt Gelareh Mazarei
Within the past decade, there has been increasing interest in the role of tryptophan (Trp) metabolites and the kynurenine pathway (KP) in diseases of the brain such as Huntington's disease (HD). Evidence is accumulating to suggest that this...
Jody Corey-Bloom,Haiqun Jia,Alaina M Aikin et al. Jody Corey-Bloom et al.
Background: Deficiencies in brain-derived-neurotrophic-factor have been implicated in the pathogenesis of Huntington's disease (HD). Objective: ...
Nektarios K Mazarakis,Christina Mo,Thibault Renoir et al. Nektarios K Mazarakis et al.
Background: Huntington's disease (HD) is caused by a tandem repeat expansion and involves progressive cognitive decline, psychiatric abnormalities and motor deficits. Disease onset and progression in HD mice can be substa...
Susanna Waters,Henrik Ponten,Daniel Klamer et al. Susanna Waters et al.
Background: The efficacy of the dopaminergic stabilizer, pridopidine, in reducing the voluntary and involuntary motor symptoms of Huntington's disease (HD) is under clinical evaluation. Tetrabenazine is currently the only...