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Plos One|June 20, 2015
Exonic Re-Sequencing of the Chromosome 2q24.3 Parkinson's Disease LocusCatherine Labbé, Kotaro Ogaki, Oswaldo Lorenzo-Betancor, et al.
Parkinsonism & Related Disorders|July 28, 2009
A Swedish family with de novo alpha-synuclein A53T mutation: evidence for early cortical dysfunctionAndreas Puschmann, Owen A Ross, Carles Vilariño-Güell, et al.
Annals of Neurology|June 24, 2008
Genomic investigation of alpha-synuclein multiplication and parkinsonismOwen A Ross, Adam T Braithwaite, Lisa M Skipper, et al.
Molecular Neurodegeneration|July 11, 2018
Replication of progressive supranuclear palsy genome-wide association study identifies SLCO1A2 and DUSP10 as new susceptibility lociMonica Y Sanchez-Contreras, Naomi Kouri, Casey N Cook, et al.
Stroke|June 23, 2020
Efficacy of Clopidogrel for Prevention of Stroke Based on CYP2C19 Allele Status in the POINT TrialJames F Meschia, Ronald L Walton, Luca P Farrugia, et al.
Neurology. Genetics|July 24, 2025
Combating Genetic Heterogeneity for Polygenic Prediction of Susceptibility to Brain β-Amyloid Deposition: Beyond APOEVijay K Ramanan, Michael G Heckman, Ekaterina I Hofrenning, et al.
Neurobiology of Aging|February 6, 2018
Insufficient evidence for pathogenicity of SNCA His50Gln (H50Q) in Parkinson's diseaseCornelis Blauwendraat, Demis A Kia, Lasse Pihlstrøm, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|November 1, 2011
LRRK2 haplotype-sharing analysis in Parkinson's disease reveals a novel p.S1761R mutationOswaldo Lorenzo-Betancor, Lluís Samaranch, Mario Ezquerra, et al.
Annals of Neurology|January 25, 2020
Fine-Mapping of SNCA in Rapid Eye Movement Sleep Behavior Disorder and Overt SynucleinopathiesLynne Krohn, Richard Y J Wu, Karl Heilbron, et al.
Neurology|February 11, 2021
Association of Mitochondrial DNA Genomic Variation With Risk of Pick DiseaseRebecca R Valentino, Michael G Heckman, Patrick W Johnson, et al.
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