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Dementia and Geriatric Cognitive Disorders|November 2, 2002
Clinical and neuropathological correlates of apolipoprotein E genotype in dementia with Lewy bodiesAndrew B Singleton, Anna Wharton, Kirsty K O'Brien, et al.Neurobiology of Aging|December 26, 2009
Mutational analysis of parkin and PINK1 in multiple system atrophyJanet A Brooks, Henry Houlden, Anna Melchers, et al.Human Molecular Genetics|January 11, 2011
Distinct DNA methylation changes highly correlated with chronological age in the human brainDena G Hernandez, Michael A Nalls, J Raphael Gibbs, et al.Annals of Neurology|February 7, 2019
Shared polygenic risk and causal inferences in amyotrophic lateral sclerosisSara Bandres-Ciga, Alastair J Noyce, Gibran Hemani, et al.Stroke|March 3, 2007
IL1RN VNTR polymorphism in ischemic stroke: analysis in 3 populationsBradford B Worrall, Thomas G Brott, Robert D Brown, et al.Movement Disorders : Official Journal of the Movement Disorder Society|January 25, 2019
The endocytic membrane trafficking pathway plays a major role in the risk of Parkinson's diseaseSara Bandres-Ciga, Sara Saez-Atienzar, Luis Bonet-Ponce, et al.Movement Disorders : Official Journal of the Movement Disorder Society|September 23, 2006
Parkinson's disease due to the R1441G mutation in Dardarin: a founder effect in the BasquesJavier Simón-Sánchez, José-Félix Martí-Massó, José Vicente Sánchez-Mut, et al.Human Molecular Genetics|January 15, 2021
Assessing the relationship between monoallelic PRKN mutations and Parkinson's riskSteven J Lubbe, Bernabe I Bustos, Jing Hu, et al.Movement Disorders : Official Journal of the Movement Disorder Society|January 26, 2021
The Parkinson's Disease DNA Variant BrowserJonggeol J Kim, Mary B Makarious, Sara Bandres-Ciga, et al.Journal of Medical Genetics|February 10, 2006
Testing association between LRRK2 and Parkinson's disease and investigating linkage disequilibriumC Paisán-Ruíz, E W Evans, S Jain, et al.Pageof 48