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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
Bronwyn Moorhouse,Caroline A Fisher Bronwyn Moorhouse
Dysphagia is a very common occurrence in Huntington's disease (HD). As such, many people with HD require texture modified diets. This commentary discusses the implications for individuals living long-term on modified diets, including the lo...
Andrew Christopher McCourt,Jennifer Parker,Edina Silajdžić et al. Andrew Christopher McCourt et al.
Background: In addition to classical neurological symptoms, Huntington's disease (HD) is complicated by peripheral pathology and both the mutant gene and the protein are found in cells and tissues throughout the body. Des...
George McNally,Hugh Rickards,Mike Horton et al. George McNally et al.
Background: The short version of the Problem Behaviours Assessment (PBA-s) is the recommended outcome measure for behavioural symptoms in Huntington's disease. Rasch analysis was used to further investigate the measuremen...
Sarah Gregory,James H Cole,Ruth E Farmer et al. Sarah Gregory et al.
Background: Huntington's disease is marked by progressive neuroanatomical changes, assumed to underlie the development of the disease's characteristic symptoms. Previous work has demonstrated longitudinal macrostructural ...
Govinda R Poudel,Shannon Driscoll,Juan F Domínguez D et al. Govinda R Poudel et al.
Background: Neuropsychiatric disturbances are common in Huntington's Disease (HD) and have been observed in gene-positive individuals several years prior to the onset of motor symptoms. The neural mechanism underpinning t...
Andreas-Antonios Roussakis,Paola Piccini Andreas-Antonios Roussakis
To date, little is known about how neurodegeneration and neuroinflammation propagate in Huntington's disease (HD). Unfortunately, no treatment is available to cure or reverse the progressive decline of function caused by the disease, thus c...
Abhishek Lenka,Nitish L Kamble,V Sowmya et al. Abhishek Lenka et al.
Background: Huntington's disease (HD) is a genetically mediated neurodegenerative disorder characterized by presence of involuntary movements, behavioral problems and cognitive dysfunctions. Though few patients with HD ma...
Fabian Kreilaus,Adena S Spiro,Anthony J Hannan et al. Fabian Kreilaus et al.
Background: Cholesterol has essential functions in neurological processes that require tight regulation of synthesis and metabolism. Perturbed cholesterol homeostasis has been demonstrated in Huntington's disease, however...
Thibault Renoir,Terence Y Pang,Yoshiko Shikano et al. Thibault Renoir et al.
Background: We previously reported sex differences in depression-like behaviours in a mouse model of Huntington's disease (HD). Objective: ...
Aaron A Sorensen,M&#x;hamed El Aisati,David Weedon Aaron A Sorensen
Huntington's disease (HD), research has grown dramatically over the last 25 years of research to the point where an analysis of productivity is warranted. We have compiled a list of the 100 most-cited researchers in HD together with H-Indic...