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Biorxiv : the Preprint Server for Biology|April 8, 2024
GenoTools: An Open-Source Python Package for Efficient Genotype Data Quality Control and AnalysisDan Vitale, Mathew Koretsky, Nicole Kuznetsov, et al.Parkinsonism & Related Disorders|June 3, 2014
Three families with Perry syndrome from distinct parts of the worldPawel Tacik, Fabienne C Fiesel, Shinsuke Fujioka, et al.Human Molecular Genetics|September 20, 2008
A duplication at chromosome 11q12.2-11q12.3 is associated with spinocerebellar ataxia type 20Melanie A Knight, Dena Hernandez, Scott J Diede, et al.Medrxiv : the Preprint Server for Health Sciences|January 8, 2026
The Global Parkinson's Disease Genetics (GP2) Genome BrowserZih-Hua Fang, Riley H Grant, Dan Vitale, et al.Neurology|May 7, 2013
Two-stage association study and meta-analysis of mitochondrial DNA variants in Parkinson diseaseGavin Hudson, Mike Nalls, Jonathan R Evans, et al.Journal of Neurology, Neurosurgery, and Psychiatry|November 8, 2013
Novel C12orf65 mutations in patients with axonal neuropathy and optic atrophyArianna Tucci, Yo-Tsen Liu, Elisabeth Preza, et al.Parkinsonism & Related Disorders|December 3, 2014
Three sib-pairs of autopsy-confirmed progressive supranuclear palsyShinsuke Fujioka, Monica Y Sanchez Contreras, Audrey J Strongosky, et al.Movement Disorders : Official Journal of the Movement Disorder Society|October 26, 2011
Genetic variants of α-synuclein are not associated with essential tremorOwen A Ross, Karen N Conneely, Tao Wang, et al.Neurobiology of Aging|October 22, 2013
SLC1A2 rs3794087 does not associate with essential tremorJay P Ross, Sruti Rayaprolu, Cecily Q Bernales, et al.Movement Disorders : Official Journal of the Movement Disorder Society|February 4, 2016
Cerebellar ataxia in progressive supranuclear palsy: An autopsy study of PSP-CShunsuke Koga, Keith A Josephs, Kotaro Ogaki, et al.Pageof 77