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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.
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.
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.
Neurology
|
September 13, 2013
C9ORF72 repeat expansions in cases with previously identified pathogenic mutations
Marka van Blitterswijk, Matthew C Baker, Mariely DeJesus-Hernandez, 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.
Brain : a Journal of Neurology
|
August 4, 2011
Sensitivity of revised diagnostic criteria for the behavioural variant of frontotemporal dementia
Katya Rascovsky, John R Hodges, David Knopman, et al.
Journal of Neuropathology and Experimental Neurology
|
December 28, 2020
Early Selective Vulnerability of the CA2 Hippocampal Subfield in Primary Age-Related Tauopathy
Jamie M Walker, Timothy E Richardson, Kurt Farrell, et al.
Archives of Neurology
|
April 13, 2011
Genetic and clinical features of progranulin-associated frontotemporal lobar degeneration
Alice S Chen-Plotkin, Maria Martinez-Lage, Patrick M A Sleiman, et al.
Acta Neuropathologica
|
November 1, 2021
Genome-wide association study and functional validation implicates JADE1 in tauopathy
Kurt Farrell, SoongHo Kim, Natalia Han, et al.
Page
of 27
Search research articles
Search
Showing results (241-250 of 263) with videos related to
Sort By:
Page
of 27
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.
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.
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.
Neurology
|
September 13, 2013
C9ORF72 repeat expansions in cases with previously identified pathogenic mutations
Marka van Blitterswijk, Matthew C Baker, Mariely DeJesus-Hernandez, 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.
Brain : a Journal of Neurology
|
August 4, 2011
Sensitivity of revised diagnostic criteria for the behavioural variant of frontotemporal dementia
Katya Rascovsky, John R Hodges, David Knopman, et al.
Journal of Neuropathology and Experimental Neurology
|
December 28, 2020
Early Selective Vulnerability of the CA2 Hippocampal Subfield in Primary Age-Related Tauopathy
Jamie M Walker, Timothy E Richardson, Kurt Farrell, et al.
Archives of Neurology
|
April 13, 2011
Genetic and clinical features of progranulin-associated frontotemporal lobar degeneration
Alice S Chen-Plotkin, Maria Martinez-Lage, Patrick M A Sleiman, et al.
Acta Neuropathologica
|
November 1, 2021
Genome-wide association study and functional validation implicates JADE1 in tauopathy
Kurt Farrell, SoongHo Kim, Natalia Han, et al.
Page
of 27