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Nature Genetics|July 26, 2005
Mutations in the endosomal ESCRTIII-complex subunit CHMP2B in frontotemporal dementiaGaia Skibinski, Nicholas J Parkinson, Jeremy M Brown, et al.
Neurology|September 2, 2016
Serum neurofilament light chain protein is a measure of disease intensity in frontotemporal dementiaJonathan D Rohrer, Ione O C Woollacott, Katrina M Dick, et al.
Neurobiology of Aging|September 28, 2015
Genetic determinants of white matter hyperintensities and amyloid angiopathy in familial Alzheimer's diseaseNatalie S Ryan, Geert-Jan Biessels, Lois Kim, et al.
Open Biology|December 4, 2015
A systematic investigation of production of synthetic prions from recombinant prion proteinChristian Schmidt, Jeremie Fizet, Francesca Properzi, et al.
Brain : a Journal of Neurology|April 23, 2021
Plasma amyloid-β ratios in autosomal dominant Alzheimer's disease: the influence of genotypeAntoinette O'Connor, Josef Pannee, Teresa Poole, et al.
The New England Journal of Medicine|November 16, 2012
TREM2 variants in Alzheimer's diseaseRita Guerreiro, Aleksandra Wojtas, Jose Bras, et al.
Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association|March 20, 2016
Genetic risk factors for the posterior cortical atrophy variant of Alzheimer's diseaseJonathan M Schott, Sebastian J Crutch, Minerva M Carrasquillo, et al.
Molecular Psychiatry|July 16, 2020
Plasma phospho-tau181 in presymptomatic and symptomatic familial Alzheimer's disease: a longitudinal cohort studyAntoinette O'Connor, Thomas K Karikari, Teresa Poole, et al.
Brain : a Journal of Neurology|September 13, 2011
Clinical and neuroanatomical signatures of tissue pathology in frontotemporal lobar degenerationJonathan D Rohrer, Tammaryn Lashley, Jonathan M Schott, et al.
Acta Neuropathologica|May 22, 2010
FUS pathology defines the majority of tau- and TDP-43-negative frontotemporal lobar degenerationHazel Urwin, Keith A Josephs, Jonathan D Rohrer, et al.
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