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Developing effective treatments for neurodegenerative diseases is one of the greatest medical challenges of the 21st century.
Parkinson�s disease (PD) and dementia with Lewy bodies (DLB) are very common neurological disorders of the elderly.
Although many of these clinical entities have been recognized for more than a hundred years, it is only during the past ten years
that the molecular events that precipitate disease have begun to be understood. Mutations in the alpha-synuclein gene cause PD,
often associated with dementia. Neuropathologically these diseases are characterized by the presence of Lewy bodies, intraneuronal
inclusions mostly composed of alpha-synuclein protein fibrils. Despite the progress that has been made in understanding the
underlying disease mechanisms of PD and DLB, there remains an urgent need to develop methods for use in diagnosis. The
development of reliable surrogate markers for the presence and abundance of alpha-synuclein lesions (Lewy bodies) in the brain
would naturally facilitate a more streamlined work-up during the early care of PD and DLB patients, and importantly, allow for the
biologically guided evaluation of future drug trials aimed at neuroprotection in the synucleinopathies. In this seminar, the author
will review the latest findings in genetics and biomarkers discovery for PD and related disorders.