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Journal of Neuropathology and Experimental Neurology
|
April 11, 2012
Correlation of Alzheimer disease neuropathologic changes with cognitive status: a review of the literature
Peter T Nelson, Irina Alafuzoff, Eileen H Bigio, et al.
Neurobiology of Aging
|
May 29, 2014
Ataxin-2 as potential disease modifier in C9ORF72 expansion carriers
Marka van Blitterswijk, Bianca Mullen, Michael G Heckman, et al.
Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association
|
October 16, 2012
The advantages of frontotemporal degeneration drug development (part 2 of frontotemporal degeneration: the next therapeutic frontier)
Adam L Boxer, Michael Gold, Edward Huey, et al.
Molecular Neurodegeneration
|
September 21, 2014
Genetic modifiers in carriers of repeat expansions in the C9ORF72 gene
Marka van Blitterswijk, Bianca Mullen, Aleksandra Wojtas, et al.
Acta Neuropathologica
|
January 4, 2014
TMEM106B protects C9ORF72 expansion carriers against frontotemporal dementia
Marka van Blitterswijk, Bianca Mullen, Alexandra M Nicholson, et al.
Alzheimer'S & Dementia (Amsterdam, Netherlands)
|
May 14, 2023
Feasibility and acceptability of remote smartphone cognitive testing in frontotemporal dementia research
Jack Carson Taylor, Hilary W Heuer, Annie L Clark, et al.
Neuron
|
August 18, 2017
TIA1 Mutations in Amyotrophic Lateral Sclerosis and Frontotemporal Dementia Promote Phase Separation and Alter Stress Granule Dynamics
Ian R Mackenzie, Alexandra M Nicholson, Mohona Sarkar, et al.
Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association
|
December 25, 2025
Clinical Manifestations
Celine N Sakran, Juan-Camilo Vargas-González, Nico Paulo Dimal, et al.
Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association
|
December 24, 2025
Clinical Manifestations
Juan-Camilo Vargas-González, Hessah A Alotibi, Kasey Cortez, et al.
The Lancet. Neurology
|
September 11, 2007
Phenotypic variability associated with progranulin haploinsufficiency in patients with the common 1477C-->T (Arg493X) mutation: an international initiative
Rosa Rademakers, Matt Baker, Jennifer Gass, et al.
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of 14
Search research articles
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Showing results (101-110 of 134) with videos related to
Sort By:
Page
of 14
Journal of Neuropathology and Experimental Neurology
|
April 11, 2012
Correlation of Alzheimer disease neuropathologic changes with cognitive status: a review of the literature
Peter T Nelson, Irina Alafuzoff, Eileen H Bigio, et al.
Neurobiology of Aging
|
May 29, 2014
Ataxin-2 as potential disease modifier in C9ORF72 expansion carriers
Marka van Blitterswijk, Bianca Mullen, Michael G Heckman, et al.
Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association
|
October 16, 2012
The advantages of frontotemporal degeneration drug development (part 2 of frontotemporal degeneration: the next therapeutic frontier)
Adam L Boxer, Michael Gold, Edward Huey, et al.
Molecular Neurodegeneration
|
September 21, 2014
Genetic modifiers in carriers of repeat expansions in the C9ORF72 gene
Marka van Blitterswijk, Bianca Mullen, Aleksandra Wojtas, et al.
Acta Neuropathologica
|
January 4, 2014
TMEM106B protects C9ORF72 expansion carriers against frontotemporal dementia
Marka van Blitterswijk, Bianca Mullen, Alexandra M Nicholson, et al.
Alzheimer'S & Dementia (Amsterdam, Netherlands)
|
May 14, 2023
Feasibility and acceptability of remote smartphone cognitive testing in frontotemporal dementia research
Jack Carson Taylor, Hilary W Heuer, Annie L Clark, et al.
Neuron
|
August 18, 2017
TIA1 Mutations in Amyotrophic Lateral Sclerosis and Frontotemporal Dementia Promote Phase Separation and Alter Stress Granule Dynamics
Ian R Mackenzie, Alexandra M Nicholson, Mohona Sarkar, et al.
Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association
|
December 25, 2025
Clinical Manifestations
Celine N Sakran, Juan-Camilo Vargas-González, Nico Paulo Dimal, et al.
Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association
|
December 24, 2025
Clinical Manifestations
Juan-Camilo Vargas-González, Hessah A Alotibi, Kasey Cortez, et al.
The Lancet. Neurology
|
September 11, 2007
Phenotypic variability associated with progranulin haploinsufficiency in patients with the common 1477C-->T (Arg493X) mutation: an international initiative
Rosa Rademakers, Matt Baker, Jennifer Gass, et al.
Page
of 14