Huntington’s disease (HD) is caused by the expansion of a CAG repeat in the huntingtin (HTT) gene. The R6 mouse models of HD express a mutant version of exon 1 HTT and typically develop motor and cogn

NIAID Data Ecosystem40

Demographic and clinical characteristics of study cohort.

神经退行性疾病表型

认知功能评估

Maximum score for each test in brackets where applicable. *p<.05; **p<.005; ***p<.0001; n/s = not significant; n/a = not applicable; bvFTD = behavioural-variant frontotemporal dementia; SD = semantic

NIAID Data Ecosystem30

Natural history, phenotypic spectrum, and discriminative features of multisystemic RFC1-disease

神经退行性疾病表型

RFC1基因

Objective: To delineate the full phenotypic spectrum, discriminative features, piloting longitudinal progression data, and sample size calculations of RFC1-repeat expansions, recently identified as ca

NIAID Data Ecosystem40

Demographic and clinical information of two Parkinson’s disease sub-groups.

帕金森病亚型

神经退行性疾病表型

Demographic and clinical information of two Parkinson’s disease sub-groups.

Figshare2016-02-23 更新30