Abstract
Parkinson’s disease (PD) is traditionally defined as a clinico-pathologic entity, characterized by a core syndrome of akinesia, rigidity, tremor, and postural instability, and pathologically by a more or less selective degeneration of dopaminergic neurons of the substantia nigra, leading to a deficiency of dopamine in the striatal projection areas of these neurons. Characteristic eosinophilic inclusions, the Lewy bodies (LBs), are found in surviving dopaminergic neurons but also, although less abundantly, in other parts of the brain in most cases (1).
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Gasser, T. (2005). Genetics of Atypical Parkinsonism. In: Litvan, I. (eds) Atypical Parkinsonian Disorders. Current Clinical Neurology. Humana Press. https://doi.org/10.1385/1-59259-834-X:139
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