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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
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David Bourke,Gregory Finucane,Jo Dysart et al. David Bourke et al.
We aimed to determine if the appointment of a Huntington's disease (HD) nurse specialist has influenced inpatient admission rates and admission quality at Auckland Hospital. We collated HD inpatient admission data for the 32 months before a...
Laurie Galvan,Véronique M André,Elizabeth A Wang et al. Laurie Galvan et al.
There is morphological evidence for differential alterations in striatal medium-sized spiny neurons (MSNs) giving rise to the direct and indirect output pathways in Huntington's disease (HD). MSNs of the indirect pathway appear to be partic...
Asa Petersén,Sanaz Gabery Asa Petersén
Huntington's disease (HD) is a neurodegenerative disorder caused by an expanded CAG repeat in the huntingtin gene. Today, the clinical diagnosis of the disease requires unequivocal signs of typical motor disturbances, which is thought to be...
Alice Wexler Alice Wexler
Although the disease today known as Huntington's was described as early as the mid-19th century, knowledgeable physicians despaired of finding successful therapies and affected families largely kept it hidden. Starting in the late 1960 s, t...
Angelica Vittori,Michael Orth,Raymund A C Roos et al. Angelica Vittori et al.
Background: Huntington's disease (HD) is an autosomal dominant neurodegenerative disorder caused by the abnormal expansion of a CAG triplet repeat tract in the huntingtin gene. While the length of this CAG expansion is th...
Kevin H J Park,Ge Lu,Jing Fan et al. Kevin H J Park et al.
Huntington's disease (HD) is a progressive neurodegenerative disorder caused by an expanded CAG trinucleotide repeat sequence in the huntingtin gene. The resulting poly-glutamine expansion in the huntingtin protein imparts a novel toxic gai...
Nigel I Wood,Stephen J Sawiak,Guido Buonincontri et al. Nigel I Wood et al.
HD is a progressive genetic neurological disorder, characterized by motor as well as cognitive impairments. The gene carrying the mutation causing Huntington's disease (HD) is not brain specific, and there is increasing evidence for periphe...
Emily Mitchell Sontag,Gregor P Lotz,Guocheng Yang et al. Emily Mitchell Sontag et al.
The Huntington's disease (HD) mutation leads to a complex process of Huntingtin (Htt) aggregation into multimeric species that eventually form visible inclusions in cytoplasm, nuclei and neuronal processes. One hypothesis is that smaller, s...
Melissa K Strong,Amber L Southwell,Jennifer M Yonan et al. Melissa K Strong et al.
Mouse strain background can influence vulnerability to excitotoxic neuronal cell death and potentially modulate phenotypes in transgenic mouse models of human disease. Evidence supports a contribution of excitotoxicity to the selective deat...