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Neurobiology of Aging|September 18, 2013
Assessing the role of the TREM2 p.R47H variant as a risk factor for Alzheimer's disease and frontotemporal dementiaAgustín Ruiz, Oriol Dols-Icardo, María J Bullido, et al.Parkinsonism & Related Disorders|December 6, 2020
Exome-wide rare variant analysis in familial essential tremorMonica Diez-Fairen, Gabrielle Houle, Sara Ortega-Cubero, et al.Journal of Alzheimer'S Disease : JAD|October 8, 2015
MAPT H1 Haplotype is Associated with Late-Onset Alzheimer's Disease Risk in APOEɛ4 Noncarriers: Results from the Dementia Genetics Spanish ConsortiumPau Pastor, Fermín Moreno, Jordi Clarimón, et al.Neurobiology of Aging|March 23, 2015
Genetic variability in SQSTM1 and risk of early-onset Alzheimer dementia: a European early-onset dementia consortium studyElise Cuyvers, Julie van der Zee, Karolien Bettens, et al.Human Mutation|September 29, 2015
Rare Variants in PLD3 Do Not Affect Risk for Early-Onset Alzheimer Disease in a European Consortium CohortRita Cacace, Tobi Van den Bossche, Sebastiaan Engelborghs, et al.Neurobiology of Aging|July 22, 2014
Investigation of the role of rare TREM2 variants in frontotemporal dementia subtypesMathias Thelen, Cristina Razquin, Isabel Hernández, et al.Human Molecular Genetics|June 29, 2014
Genetic analysis implicates APOE, SNCA and suggests lysosomal dysfunction in the etiology of dementia with Lewy bodiesJose Bras, Rita Guerreiro, Lee Darwent, et al.Acta Neuropathologica|April 28, 2017
Deleterious ABCA7 mutations and transcript rescue mechanisms in early onset Alzheimer's diseaseArne De Roeck, Tobi Van den Bossche, Julie van der Zee, et al.Neurobiology of Aging|December 9, 2015
Genome-wide analysis of genetic correlation in dementia with Lewy bodies, Parkinson's and Alzheimer's diseasesRita Guerreiro, Valentina Escott-Price, Lee Darwent, et al.Brain : a Journal of Neurology|November 1, 2016
Genome-wide association study in essential tremor identifies three new lociStefanie H Müller, Simon L Girard, Franziska Hopfner, et al.Pageof 5