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Parkinsonism & Related Disorders|April 3, 2007
Identification of potential protein interactors of Lrrk2Justus C Dächsel, Julie P Taylor, Su San Mok, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|November 2, 2017
Establishing diagnostic criteria for Perry syndromeTakayasu Mishima, Shinsuke Fujioka, Hiroyuki Tomiyama, et al.
Neurologia I Neurochirurgia Polska|July 21, 2020
Spinocerebellar ataxia type 6 family with phenotypic overlap with Multiple System AtrophyRana Hanna Al-Shaikh, Anna I Wernick, Audrey J Strongosky, et al.
Nature Communications|August 22, 2022
Epigenome-wide association study of human frontal cortex identifies differential methylation in Lewy body pathologyLasse Pihlstrøm, Gemma Shireby, Hanneke Geut, et al.
Journal of Alzheimer'S Disease & Parkinsonism|July 21, 2025
A Blood Screening Test for Dementia with Lewy Bodies for Primary CareMelissa Petersen, Tanis J Ferman, Fan Zhang, et al.
The Journals of Gerontology. Series A, Biological Sciences and Medical Sciences|October 2, 2019
CLEC3B p.S106G Mutant in a Caucasian Population of Successful Neurological AgingAna Kolicheski, Ronald L Walton, Alexandra I Soto-Beasley, et al.
Parkinsonism & Related Disorders|March 21, 2020
Prevalence of GBA p.K198E mutation in Colombian and Hispanic populationsPhilip W Tipton, Alexandra I Soto-Beasley, Ronald L Walton, et al.
Parkinsonism & Related Disorders|April 3, 2007
Lack of evidence for association of Parkin promoter polymorphism (PRKN-258) with increased risk of Parkinson's diseaseOwen A Ross, Kristoffer Haugarvoll, Jeremy T Stone, et al.
BMC Medical Genetics|March 20, 2012
Polymorphic genes of detoxification and mitochondrial enzymes and risk for progressive supranuclear palsy: a case control studyLisa F Potts, Alex C Cambon, Owen A Ross, et al.
European Journal of Neurology|August 3, 2021
Clinical, pathological and genetic characteristics of Perry disease-new cases and literature reviewJarosław Dulski, Catalina Cerquera-Cleves, Lukasz Milanowski, et al.
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