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• W2225712950 abstract "It has been recognized for many years that a number of chronic neurodegenerative diseases of the CNS are characterized by the development of intracellular inclusion bodies, but it is only relatively recently that the core proteins defining these pathologies have been defined. One such protein is alpha synuclein, that was found to be the main component of Lewy bodies in the late 1990s, and this discovery reinforced the emerging view that alpha synuclein was intimately linked to diseases characterized by this type of pathology – namely Parkinson's disease (PD) and Dementia with Lewy Bodies (DLB). Furthermore at around this time, this same protein was also found within the glial inclusion bodies of patients dying with multiple system atrophy (MSA). These three disorders constitute the majority of patients with an ‘alpha synucleinopathy’, although there are a number of rarer conditions that can also cause this pathology including inherited metabolic disorders such as Gaucher's disease (GD). In this review, we will concentrate on PD, the commonest alpha synucleinopathy, and its associated dementia (PDD), as well as discussing DLB and MSA and will highlight how the clinical features of these conditions vary as a function of pathology." @default.
• W2225712950 created "2016-06-24" @default.
• W2225712950 creator A5052579930 @default.
• W2225712950 creator A5084748006 @default.
• W2225712950 date "2016-02-01" @default.
• W2225712950 modified "2023-10-13" @default.
• W2225712950 title "Review: The spectrum of clinical features seen with alpha synuclein pathology" @default.
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• W2225712950 doi "https://doi.org/10.1111/nan.12303" @default.
• W2225712950 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/26750431" @default.
• W2225712950 hasPublicationYear "2016" @default.
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