Titlebook: Biomarkers for Huntington‘s Disease; Improving Clinical O Elizabeth A. Thomas,Georgia M. Parkin Book 2023 The Editor(s) (if applicable) and

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https://doi.org/10.1007/978-3-658-20524-9his results in a widespread dysregulation of cellular pathways and death of medium spiny neurons of the striatum. Due to the high metabolic demand of brain tissue, mitochondrial dysfunction and resulting oxidative stress are common pathological features contributing to many neurodegenerative disease

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Beiträge zum Diversity Managementscovery of aggregated TDP-43 as a pathological hallmark in Frontotemporal Lobar Degeneration and Amyotrophic Lateral Sclerosis (ALS) in 2006, this protein has been predominantly linked to neurodegenerative diseases. The pathophysiological role of aggregated TDP-43 in these diseases is not completely

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https://doi.org/10.1007/978-3-031-32815-2neurodegeneration; chorea; movement disorders; Huntington‘s disease; biofluids; biomarkers; imaging bioma

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Contemporary Clinical Neurosciencehttp://image.papertrans.cn/b/image/187798.jpg

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The Utility of Biomarkers for Huntington’s Diseaseons and cognitive decline. The specific mutation responsible for HD is an expanded CAG repeat in exon 1 of the Huntington gene. This mutation can now be easily detected through genetic testing, allowing for confirmation of the genetic status in individuals at risk of developing HD, which occurs at a