Showing results (241-250 of 477) with videos related to

Sort By:
Pageof 48
Brain : a Journal of Neurology|June 29, 2012
Exome sequencing reveals riboflavin transporter mutations as a cause of motor neuron diseaseJanel O Johnson, J Raphael Gibbs, Andre Megarbane, et al.
The Lancet. Neurology|February 5, 2008
DYT16, a novel young-onset dystonia-parkinsonism disorder: identification of a segregating mutation in the stress-response protein PRKRASarah Camargos, Sonja Scholz, Javier Simón-Sánchez, et al.
Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association|May 21, 2024
A cross-sectional study of α-synuclein seed amplification assay in Alzheimer's disease neuroimaging initiative: Prevalence and associations with Alzheimer's disease biomarkers and cognitive functionDuygu Tosun, Zachary Hausle, Hirotaka Iwaki, et al.
Nucleic Acids Research|February 26, 2013
Resolving the polymorphism-in-probe problem is critical for correct interpretation of expression QTL studiesAdaikalavan Ramasamy, Daniah Trabzuni, J Raphael Gibbs, et al.
Neurobiology of Aging|October 14, 2014
Analysis of C9orf72 repeat expansions in a large series of clinically and pathologically diagnosed cases with atypical parkinsonismLucia V Schottlaender, James M Polke, Helen Ling, et al.
Nature Genetics|September 12, 2017
A meta-analysis of genome-wide association studies identifies 17 new Parkinson's disease risk lociDiana Chang, Mike A Nalls, Ingileif B Hallgrímsdóttir, et al.
International Journal of Geriatric Psychiatry|February 2, 2019
A candidate gene study of risk for dementia in older, postmenopausal women: Results from the Women's Health Initiative Memory StudyIra Driscoll, Beverly M Snively, Mark A Espeland, et al.
British Journal of Neurosurgery|July 10, 2020
Extended lumbar drainage in idiopathic normal pressure hydrocephalus: a systematic review and meta-analysis of diagnostic test accuracyAdam C Nunn, Hayley E Jones, Cezar O Morosanu, et al.
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.
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.
Pageof 48