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Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association
|
October 14, 2025
Cross-country variance in facial emotion recognition in presymptomatic and symptomatic behavioral variant frontotemporal dementia: Insights from the GENFI and ReDLat consortia
Liset de Boer, Lize C Jiskoot, Harro Seelaar, et al.
Brain : a Journal of Neurology
|
April 22, 2025
Disease-modifying effects of TMEM106B in genetic frontotemporal dementia: a longitudinal GENFI study
Saira S Mirza, Maurice Pasternak, Andrew D Paterson, et al.
Brain : a Journal of Neurology
|
October 11, 2021
A data-driven disease progression model of fluid biomarkers in genetic frontotemporal dementia
Emma L van der Ende, Esther E Bron, Jackie M Poos, et al.
Acta Neuropathologica
|
April 28, 2017
Deleterious ABCA7 mutations and transcript rescue mechanisms in early onset Alzheimer's disease
Arne De Roeck, Tobi Van den Bossche, Julie van der Zee, et al.
Neurology
|
September 16, 2024
Frequency and Longitudinal Course of Behavioral and Neuropsychiatric Symptoms in Participants With Genetic Frontotemporal Dementia
Sonja Schönecker, Francisco J Martinez-Murcia, Jannis Denecke, et al.
The Lancet. Neurology
|
November 9, 2019
Serum neurofilament light chain in genetic frontotemporal dementia: a longitudinal, multicentre cohort study
Emma L van der Ende, Lieke H Meeter, Jackie M Poos, et al.
Annals of Clinical and Translational Neurology
|
May 16, 2018
Poly(GP), neurofilament and grey matter deficits in <i>C9orf72</i> expansion carriers
Lieke H H Meeter, Tania F Gendron, Ana C Sias, et al.
Brain : a Journal of Neurology
|
December 4, 2025
Distinct proteomic CSF profiles in genetic frontotemporal lobar degeneration
Julie F H De Houwer, Elise G Dopper, Renee van Buuren, et al.
Translational Psychiatry
|
February 2, 2019
Transethnic meta-analysis of rare coding variants in PLCG2, ABI3, and TREM2 supports their general contribution to Alzheimer's disease
Maria Carolina Dalmasso, Luis Ignacio Brusco, Natividad Olivar, et al.
Human Mutation
|
November 1, 2012
A pan-European study of the C9orf72 repeat associated with FTLD: geographic prevalence, genomic instability, and intermediate repeats
Julie van der Zee, Ilse Gijselinck, Lubina Dillen, et al.
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Search research articles
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Showing results (221-230 of 267) with videos related to
Sort By:
Page
of 27
Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association
|
October 14, 2025
Cross-country variance in facial emotion recognition in presymptomatic and symptomatic behavioral variant frontotemporal dementia: Insights from the GENFI and ReDLat consortia
Liset de Boer, Lize C Jiskoot, Harro Seelaar, et al.
Brain : a Journal of Neurology
|
April 22, 2025
Disease-modifying effects of TMEM106B in genetic frontotemporal dementia: a longitudinal GENFI study
Saira S Mirza, Maurice Pasternak, Andrew D Paterson, et al.
Brain : a Journal of Neurology
|
October 11, 2021
A data-driven disease progression model of fluid biomarkers in genetic frontotemporal dementia
Emma L van der Ende, Esther E Bron, Jackie M Poos, et al.
Acta Neuropathologica
|
April 28, 2017
Deleterious ABCA7 mutations and transcript rescue mechanisms in early onset Alzheimer's disease
Arne De Roeck, Tobi Van den Bossche, Julie van der Zee, et al.
Neurology
|
September 16, 2024
Frequency and Longitudinal Course of Behavioral and Neuropsychiatric Symptoms in Participants With Genetic Frontotemporal Dementia
Sonja Schönecker, Francisco J Martinez-Murcia, Jannis Denecke, et al.
The Lancet. Neurology
|
November 9, 2019
Serum neurofilament light chain in genetic frontotemporal dementia: a longitudinal, multicentre cohort study
Emma L van der Ende, Lieke H Meeter, Jackie M Poos, et al.
Annals of Clinical and Translational Neurology
|
May 16, 2018
Poly(GP), neurofilament and grey matter deficits in <i>C9orf72</i> expansion carriers
Lieke H H Meeter, Tania F Gendron, Ana C Sias, et al.
Brain : a Journal of Neurology
|
December 4, 2025
Distinct proteomic CSF profiles in genetic frontotemporal lobar degeneration
Julie F H De Houwer, Elise G Dopper, Renee van Buuren, et al.
Translational Psychiatry
|
February 2, 2019
Transethnic meta-analysis of rare coding variants in PLCG2, ABI3, and TREM2 supports their general contribution to Alzheimer's disease
Maria Carolina Dalmasso, Luis Ignacio Brusco, Natividad Olivar, et al.
Human Mutation
|
November 1, 2012
A pan-European study of the C9orf72 repeat associated with FTLD: geographic prevalence, genomic instability, and intermediate repeats
Julie van der Zee, Ilse Gijselinck, Lubina Dillen, et al.
Page
of 27