Correlations of plasma glial fibrillary acidic protein levels with glymphatic system impairment in Huntington’s disease
Objective: To investigate whether plasma glial fibrillary acidic protein (GFAP) levels are related to glymphatic system function in Huntington's disease (HD). Background: Plasma GFAP levels has…Hashimoto Encephalopathy, A Choreiform Presentation
Objective: We report the case of a woman with chorea as lonely feature Background: Hashimoto encephalopathy is a rare autoimmune and vasculitis encephalopathy. The first…Blood-based somatic CAG repeat expansion and clinical progression in Huntington’s disease patients from Western China
Objective: To investigate the association between blood-based somatic CAG repeat expansion ratio (SER) and clinical characteristics in Huntington’s disease (HD) patients from Western China. Background:…Cryptococcal meningitis as a rare cause of acute generalized chorea: a report of an interesting case
Objective: To describe a case with cryptococcal meningitis as a rare cause of adult-onset acute generalized chorea. Background: Chorea is an abnormal movement characterized as…Baseline lipid traits and the clinical characteristics and disease progression in Huntington’s disease
Objective: To clarify the relationship between the baseline serum lipid traits and the clinical characteristics and disease progression in a well-established cohort of Chinese HD…Challenges of Huntington’s disease and chorea in Guinea: the benefits of genetic testing in tropical environments
Objective: The aim of this study was to identify the genetic underlier of individuals presenting with chorea, allowing for the diagnosis of these patients, and…Ataxia and Parkinsonism Related with CAG Expansion Size in a Cohort of Huntington’s Disease in the Brazilian Amazon Region.
Objective: We conducted genetic and clinical assessments in 22 families, with genetic diagnosis in 51 patients with HD in the state of Amazon, Brazil. The main objectives are evaluating demographics, genetic characteristics,…Spectrum of Non-HD Hereditary Chorea- Case Series from An Indian Movement Disorder Centre
Objective: To identify and characterize the hereditary chorea other than Huntington’s disease (HD) in an Indian movement disorder clinic. Background: Approximately 1-3% of HD phenotypes…Assessing Executive Function in HD: Comparing the One Touch Stockings of Cambridge and Zindametrix’s Tower-Z as Components of the HD-CAB
Objective: To assess the comparability of performance by people with Huntington’s disease (HD) on two tower tasks. Background: Cognitive decline is a hallmark feature of…Chorea after MRgFUS for the treatment of essential tremor: A case report
Objective: To describe a case of chorea after magnetic resonance guided focused ultrasound (MRgFUS) for the treatment of essential tremor (ET). Background: ET can provide…
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