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Human Molecular Genetics|August 16, 2012
Using genome-wide complex trait analysis to quantify 'missing heritability' in Parkinson's diseaseMargaux F Keller, Mohamad Saad, Jose Bras, et al.Human Molecular Genetics|December 11, 2012
A pathway-based analysis provides additional support for an immune-related genetic susceptibility to Parkinson's diseasePeter Holmans, Valentina Moskvina, Lesley Jones, et al.Brain : a Journal of Neurology|October 28, 2025
Predictive models for ataxia progression and conversion in spinocerebellar ataxia type 1 and 3Emilien Petit, Giulia Coarelli, David Morgan, et al.Journal of Neurology|June 1, 2024
SARA captures disparate progression and responsiveness in spinocerebellar ataxiasEmilien Petit, Tanja Schmitz-Hübsch, Giulia Coarelli, et al.Journal of Neurology, Neurosurgery, and Psychiatry|February 15, 2013
The Val158Met COMT polymorphism is a modifier of the age at onset in Parkinson's disease with a sexual dimorphismStephan Klebe, Jean-Louis Golmard, Michael A Nalls, et al.JAMA Neurology|August 8, 2013
Analysis of genome-wide association studies of Alzheimer disease and of Parkinson disease to determine if these 2 diseases share a common genetic riskValentina Moskvina, Denise Harold, GianCarlo Russo, et al.Brain : a Journal of Neurology|June 29, 2014
Modulation of the age at onset in spinocerebellar ataxia by CAG tracts in various genesSophie Tezenas du Montcel, Alexandra Durr, Peter Bauer, et al.Movement Disorders : Official Journal of the Movement Disorder Society|May 5, 2021
Regional Brain and Spinal Cord Volume Loss in Spinocerebellar Ataxia Type 3Jennifer Faber, Tamara Schaprian, Koyak Berkan, et al.American Journal of Human Genetics|November 25, 2010
Targeted next-generation sequencing of a 12.5 Mb homozygous region reveals ANO10 mutations in patients with autosomal-recessive cerebellar ataxiaSascha Vermeer, Alexander Hoischen, Rowdy P P Meijer, et al.The Lancet. Neurology|March 20, 2018
Survival in patients with spinocerebellar ataxia types 1, 2, 3, and 6 (EUROSCA): a longitudinal cohort studyAlhassane Diallo, Heike Jacobi, Arron Cook, et al.Pageof 33