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Susan Mendick

Publications -  12
Citations -  2490

Susan Mendick is an academic researcher. The author has contributed to research in topics: Diffusion MRI & Cohort study. The author has an hindex of 10, co-authored 11 publications receiving 2008 citations.

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The Parkinson Progression Marker Initiative (PPMI)

TL;DR: The Parkinson Progression Marker Initiative (PPMI) is a comprehensive observational, international, multi-center study designed to identify PD progression biomarkers both to improve understanding of disease etiology and course and to provide crucial tools to enhance the likelihood of success of PD modifying therapeutic trials.
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Association of Cerebrospinal Fluid β-Amyloid 1-42, T-tau, P-tau181, and α-Synuclein Levels With Clinical Features of Drug-Naive Patients With Early Parkinson Disease

Ju-Hee Kang, +80 more
- 01 Oct 2013 - 
TL;DR: It is found that measures of CSF Aβ1-42, T-t Tau, P-tau181, and α-synuclein have prognostic and diagnostic potential in early-stage PD.
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Heterozygosity for a mutation in the parkin gene leads to later onset Parkinson disease

Tatiana Foroud, +98 more
- 11 Mar 2003 - 
TL;DR: Mutations in the parkin gene occur among individuals with PD with an older age at onset (≥60 years) who have a positive family history of the disease, and the clinical findings of parkin-positive individuals are remarkably similar to those without mutations.
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Impaired olfaction and other prodromal features in the Parkinson At-Risk Syndrome Study.

TL;DR: Assessment of hyposmic subjects using more specific markers for degeneration, such as dopamine transporter imaging, will evaluate whether combining hyposmia and other nonmotor features is useful in assessing the risk of future neurodegeneration.
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Significant Linkage of Parkinson Disease to Chromosome 2q36-37

Nathan Pankratz, +99 more
TL;DR: This work has expanded the sample to include 150 families meeting the strictest diagnostic definition of verified PD, and performs analyses using only those pedigrees with the strongest family history of PD, which strongly suggests that variation in a gene on chromosome 2q36-37 contributes to PD susceptibility.