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Neurodegenerative diseases such as Alzheimer�s disease (AD) and Parkinson�s disease (PD) are currently considered as
protein misfolding diseases. Determination of pathogenic proteins-mostly in Cerebrospinal fluid (CSF) samples has been
proposed as a disease biological marker that can be used for diagnosis and follow up. Furthermore there are some reports that
describe protein �profiles� in CSF from carriers of neurodegenerative diseases. Due to difficulties in CSF sampling, it would
be very useful to count with reliable biomarkers in peripheral fluids. Levels of peripheral Amyloid Beta (AB), AB precursor
protein (APP) and tau, among others have been evaluated for AD diagnosis, while alpha-synuclein and DJ1 have been used as
PD biomarkers. Previously we have evaluated peripheral blood platelets tau as a reliable AD biomarker. It has been performed
measures and characterization of pathogenic proteins in blood and saliva obtained from neurodegenerative disease carriers
(PD, AD and other protein misfolding diseases) by immunoblot and ELISA analyses. The specific peripheral protein profile
that characterizes different neurodegenerative diseases is also described. Also, the relation between clinical disease features
measured with standardized clinical scales like UPDRS and MMSE and levels of pathogenic proteins in blood and saliva is
described. Finally, the relevance and implications of our analyses for diagnosis and further physiopathologycal knowledge of
these diseases is discussed.
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