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Jennifer A. Foley

Researcher at UCL Institute of Neurology

Publications -  48
Citations -  1136

Jennifer A. Foley is an academic researcher from UCL Institute of Neurology. The author has contributed to research in topics: Neuropsychology & Cognition. The author has an hindex of 14, co-authored 44 publications receiving 843 citations. Previous affiliations of Jennifer A. Foley include University of Kent & Queen's University.

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Screening for cognition and behaviour changes in ALS

TL;DR: The ECAS is an effective within-clinic assessment for ALS that determines the presence, severity and type of cognitive and/or behavioural changes, an essential first step to managing these symptoms.
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Validation of the Edinburgh Cognitive and Behavioural Amyotrophic Lateral Sclerosis Screen (ECAS): A cognitive tool for motor disorders

TL;DR: The Edinburgh Cognitive and Behaviour ALS Screen (ECAS) as discussed by the authors is a multi-domain screen designed to detect cognitive deficits in patients with motor disorders, which has been shown to have high sensitivity and specificity to impairment characteristic of ALS.
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Genotype and phenotype in Parkinson's disease: Lessons in heterogeneity from deep brain stimulation

TL;DR: Patients who underwent DBS were screened for mutations in the most common genes associated with Parkinson's disease, and the consequent genetic subgroups of patients were compared with respect to phenotype, levodopa (l‐dopa), and DBS responsiveness.
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Assessing Dual-Task Performance Using a Paper-and-Pencil Test: Normative Data

TL;DR: No age effect was detected, providing strong evidence that age does not affect dual-tasking abilities, and Psychometric data for this new assessment are presented, which may enable clinicians and researchers to use this paradigm as a means of examining attentional control in dual-Tasking.
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GBA-Associated Parkinson's Disease: Progression in a Deep Brain Stimulation Cohort.

TL;DR: GBA status appears to be an important predictor for non-motor symptom disease progression, after deep brain stimulation surgery, after Parkinson's disease patients who have undergone DBS.