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Movement Disorders : Official Journal of the Movement Disorder Society|January 19, 2007
ELAVL4, PARK10, and the CeltsKristoffer Haugarvoll, Mathias Toft, Owen A Ross, et al.
Neuroscience Letters|July 7, 2007
Lrrk2 mutations in South America: A study of Chilean Parkinson's diseaseCarolina Perez-Pastene, Stephanie A Cobb, Fernando Díaz-Grez, et al.
Parkinsonism & Related Disorders|December 13, 2012
TARDBP mutations in Parkinson's diseaseSruti Rayaprolu, Shinsuke Fujioka, Sharleen Traynor, et al.
Parkinsonism & Related Disorders|February 21, 2017
Occurrence of Crohn's disease with Parkinson's diseaseShinsuke Fujioka, Sadie E Curry, Kathleen D Kennelly, et al.
The Lancet. Neurology|February 5, 2008
DYT16, a novel young-onset dystonia-parkinsonism disorder: identification of a segregating mutation in the stress-response protein PRKRASarah Camargos, Sonja Scholz, Javier Simón-Sánchez, et al.
Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association|May 21, 2024
A cross-sectional study of α-synuclein seed amplification assay in Alzheimer's disease neuroimaging initiative: Prevalence and associations with Alzheimer's disease biomarkers and cognitive functionDuygu Tosun, Zachary Hausle, Hirotaka Iwaki, et al.
Neuroscience Letters|October 5, 2010
Mitochondrial translation initiation factor 3 polymorphism and Parkinson's diseaseBahareh Behrouz, Carles Vilariño-Güell, Michael G Heckman, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|June 30, 2009
Expanding the clinical phenotype of SNCA duplication carriersKenya Nishioka, Owen A Ross, Kenji Ishii, et al.
Neurologia I Neurochirurgia Polska|February 27, 2025
Screening for PRKN and PINK1 mutations in Ecuadorian patients with early-onset Parkinson's DiseaseTobias M Franz, Rohitha K Punathil, Alexandra I Soto-Beasley, et al.
Nucleic Acids Research|February 26, 2013
Resolving the polymorphism-in-probe problem is critical for correct interpretation of expression QTL studiesAdaikalavan Ramasamy, Daniah Trabzuni, J Raphael Gibbs, et al.
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