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Neuroreport|September 28, 2002
A novel polymorphic triplet repeat in intron five of the alpha-synuclein gene: no evidence of expansion or allelic association with idiopathic Parkinson's disease in the IrishOwen A Ross, Nuri H Awayn, Deborah McWhinney, et al.European Journal of Human Genetics : EJHG|August 14, 2014
VPS35 and DNAJC13 disease-causing variants in essential tremorAlex Rajput, Jay P Ross, Cecily Q Bernales, et al.Neurology. Genetics|January 22, 2024
Machine Learning Models of Polygenic Risk for Enhanced Prediction of Alzheimer Disease EndophenotypesNathaniel B Gunter, Robel K Gebre, Jonathan Graff-Radford, et al.Parkinsonism & Related Disorders|December 10, 2023
Genetics of Parkinson's disease heterogeneity: A genome-wide association study of clinical subtypesJarosław Dulski, Ryan J Uitti, Alexandra Beasley, et al.Acta Neuropathologica Communications|September 18, 2020
Associations of mitochondrial genomic variation with corticobasal degeneration, progressive supranuclear palsy, and neuropathological tau measuresRebecca R Valentino, Nikoleta Tamvaka, Michael G Heckman, et al.Parkinsonism & Related Disorders|April 13, 2011
Human leukocyte antigen variation and Parkinson's diseaseAndreas Puschmann, Christophe Verbeeck, Michael G Heckman, 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.Neuroscience Letters|October 5, 2010
Mitochondrial translation initiation factor 3 polymorphism and Parkinson's diseaseBahareh Behrouz, Carles Vilariño-Güell, Michael G Heckman, et al.Pageof 49