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International Journal of Geriatric Psychiatry
|
May 28, 2022
Caregiving concerns and clinical characteristics across neurodegenerative and cerebrovascular disorders in the Ontario neurodegenerative disease research initiative
Derek Beaton, Paula M McLaughlin, Joseph B Orange, et al.
Brain Communications
|
November 17, 2025
Thalamus involvement in genetic frontotemporal dementia assessed using structural and diffusion MRI: a GENFI study
Sonja Soskic, Henry F J Tregidgo, Emily G Todd, et al.
Medrxiv : the Preprint Server for Health Sciences
|
June 22, 2026
Trajectories of brain structure and function in young adult carriers of genetic frontotemporal dementia variants
Isis So, Jolina Lombardi, Adam M Staffaroni, et al.
Acta Neuropathologica
|
February 11, 2019
Genome-wide analyses as part of the international FTLD-TDP whole-genome sequencing consortium reveals novel disease risk factors and increases support for immune dysfunction in FTLD
Cyril Pottier, Yingxue Ren, Ralph B Perkerson, et al.
Nature Communications
|
April 25, 2025
Deciphering distinct genetic risk factors for FTLD-TDP pathological subtypes via whole-genome sequencing
Cyril Pottier, Fahri Küçükali, Matt Baker, et al.
Medrxiv : the Preprint Server for Health Sciences
|
July 9, 2024
Deciphering Distinct Genetic Risk Factors for FTLD-TDP Pathological Subtypes via Whole-Genome Sequencing
Cyril Pottier, Fahri Küçükali, Matt Baker, et al.
Nature Genetics
|
March 13, 2026
A repeat expansion in GOLGA8A is a major risk factor for atypical frontotemporal lobar degeneration with ubiquitin-positive inclusions
Wouter De Coster, Marleen Van den Broeck, Matt Baker, et al.
The Lancet. Neurology
|
May 5, 2018
Potential genetic modifiers of disease risk and age at onset in patients with frontotemporal lobar degeneration and GRN mutations: a genome-wide association study
Cyril Pottier, Xiaolai Zhou, Ralph B Perkerson, et al.
Medrxiv : the Preprint Server for Health Sciences
|
May 10, 2023
Creating the Pick's disease International Consortium: Association study of <i>MAPT</i> H2 haplotype with risk of Pick's disease
Rebecca R Valentino, William J Scotton, Shanu F Roemer, et al.
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of 6
Search research articles
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Showing results (51-60 of 59) with videos related to
Sort By:
Page
of 6
You have reached the last page of results.
This site can display upto 59 results.
International Journal of Geriatric Psychiatry
|
May 28, 2022
Caregiving concerns and clinical characteristics across neurodegenerative and cerebrovascular disorders in the Ontario neurodegenerative disease research initiative
Derek Beaton, Paula M McLaughlin, Joseph B Orange, et al.
Brain Communications
|
November 17, 2025
Thalamus involvement in genetic frontotemporal dementia assessed using structural and diffusion MRI: a GENFI study
Sonja Soskic, Henry F J Tregidgo, Emily G Todd, et al.
Medrxiv : the Preprint Server for Health Sciences
|
June 22, 2026
Trajectories of brain structure and function in young adult carriers of genetic frontotemporal dementia variants
Isis So, Jolina Lombardi, Adam M Staffaroni, et al.
Acta Neuropathologica
|
February 11, 2019
Genome-wide analyses as part of the international FTLD-TDP whole-genome sequencing consortium reveals novel disease risk factors and increases support for immune dysfunction in FTLD
Cyril Pottier, Yingxue Ren, Ralph B Perkerson, et al.
Nature Communications
|
April 25, 2025
Deciphering distinct genetic risk factors for FTLD-TDP pathological subtypes via whole-genome sequencing
Cyril Pottier, Fahri Küçükali, Matt Baker, et al.
Medrxiv : the Preprint Server for Health Sciences
|
July 9, 2024
Deciphering Distinct Genetic Risk Factors for FTLD-TDP Pathological Subtypes via Whole-Genome Sequencing
Cyril Pottier, Fahri Küçükali, Matt Baker, et al.
Nature Genetics
|
March 13, 2026
A repeat expansion in GOLGA8A is a major risk factor for atypical frontotemporal lobar degeneration with ubiquitin-positive inclusions
Wouter De Coster, Marleen Van den Broeck, Matt Baker, et al.
The Lancet. Neurology
|
May 5, 2018
Potential genetic modifiers of disease risk and age at onset in patients with frontotemporal lobar degeneration and GRN mutations: a genome-wide association study
Cyril Pottier, Xiaolai Zhou, Ralph B Perkerson, et al.
Medrxiv : the Preprint Server for Health Sciences
|
May 10, 2023
Creating the Pick's disease International Consortium: Association study of <i>MAPT</i> H2 haplotype with risk of Pick's disease
Rebecca R Valentino, William J Scotton, Shanu F Roemer, et al.
Page
of 6