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Medrxiv : the Preprint Server for Health Sciences|May 15, 2024
Long-read sequencing unravels the complexity of structural variants in PRKN in two individuals with early-onset Parkinson's diseaseGuillaume Cogan, Kensuke Daida, Kimberley J Billingsley, et al.
Neuroscience Letters|November 11, 2006
Digenic parkinsonism: investigation of the synergistic effects of PRKN and LRRK2Justus C Dächsel, Ignacio F Mata, Owen A Ross, et al.
Parkinsonism & Related Disorders|December 3, 2015
Association of Parkinson disease age of onset with DRD2, DRD3 and GRIN2B polymorphismsAnhar Hassan, Michael G Heckman, J E Ahlskog, et al.
Mayo Clinic Proceedings|February 10, 2015
Whole-exome sequencing as a diagnostic tool in a family with episodic ataxia type 1Pawel Tacik, Kimberly J Guthrie, Audrey J Strongosky, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|November 6, 2009
Alpha-synuclein polymorphisms are associated with Parkinson's disease in a Saskatchewan populationAlex Rajput, Carles Vilariño-Güell, Michele L Rajput, et al.
Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association|November 14, 2025
Association between visual hallucinations and α-synuclein oligomers in patients with dementia with Lewy bodiesHiroaki Sekiya, Lukas Franke, Daisuke Ono, et al.
Neuroscience Letters|November 22, 2005
The human prion gene M129V polymorphism is not associated with idiopathic Parkinson's disease in three distinct populationsSonja W Scholz, Georgia Xiromerisiou, Hon C Fung, et al.
Plos One|March 20, 2012
Cooperative genome-wide analysis shows increased homozygosity in early onset Parkinson's diseaseJavier Simón-Sánchez, Laura L Kilarski, Michael A Nalls, et al.
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