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parkinsonism cohort, the Parkinson's Progression Markers Initiative (PPMI) international
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Parkinson's disease individuals with normal cognition, 121 Parkinson's disease
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Parkinson's disease. Moreover, the hallmark Parkinson's disease pathological
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Parkinson's, the Michael J Fox Foundation for Parkinson's Research
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Parkinson's disease patients. Moreover, nigral idiopathic Parkinson's disease
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Parkinson's Genetics Program, the International Parkinson's Disease Genomics
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Parkinson's disease from healthy controls. We used the well
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- Paper Serum neuronal exosomes predict and differentiate Parkinson's disease from atypical parkinsonism.
clusterin predicts and differentiates Parkinson's disease from atypical parkinsonism.
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parkinsonism, but also rarely as typical Parkinson's disease. Majority
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Parkinson's disease have increased the scope of biological knowledge
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Parkinson's disease. Clinically, Parkinson's disease patients with GBA mutations
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Parkinson's disease cases, 13 431 Parkinson's disease proxy
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Parkinson's disease has long been considered a disorder that
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Parkinson's disease has a large heritable component and genome
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Parkinson's disease. Their application in Parkinson's disease diagnosis
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Parkinson's disease. We examined whether a genetic burden of variants
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Parkinson's disease, we performed a case-control study in two regions
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Parkinson's disease are an area of extensive research that
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Parkinson's disease: from prodrome to prevention. Oliver PJ(1)(2), Civitelli
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Parkinson's disease is a progressive neurodegenerative condition associated with
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- Paper The association between mutations in the lysosomal protein glucocerebrosidase and parkinsonism.
parkinsonism. Several different lines of research support this relationship. First
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Parkinson's disease is the second most common neurodegenerative disease
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Parkinson's disease; however, individuals with Parkinson's disease are often
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parkinsonism, which has the same clinical presentation and neuropathology as Parkinson
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Parkinson's disease. Participants in whom Parkinson's disease was diagnosed
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Parkinson's disease. These genetic variants catalyze kinase activity by substrate
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- Paper Unsupervised clustering of dopamine transporter PET imaging discovers heterogeneity of parkinsonism.
Parkinsonism has heterogeneous nature, showing distinctive patterns of disease progression
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Parkinson's disease is caused by a progressive loss of the midbrain
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- Paper Augmentation of phenotype in a transgenic Parkinson mouse heterozygous for a Gaucher mutation.
Parkinson's disease; and (ii) Lewy bodies in sporadic Parkinson
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Parkinson's disease diagnosis, and on stable doses of Parkinson
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