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Neurobiology of Aging
|
January 18, 2015
Small deletion in C9orf72 hides a proportion of expansion carriers in FTLD
Sara Rollinson, Janis Bennion Callister, Kate Young, et al.
Neurobiology of Aging
|
June 2, 2014
Exome sequencing identifies 2 novel presenilin 1 mutations (p.L166V and p.S230R) in British early-onset Alzheimer's disease
Celeste Sassi, Rita Guerreiro, Raphael Gibbs, et al.
Parkinsonism & Related Disorders
|
October 26, 2010
Glucocerebrosidase mutations in diffuse Lewy body disease
Kenya Nishioka, Owen A Ross, Carles Vilariño-Güell, et al.
Nature
|
July 25, 2006
Mutations in progranulin cause tau-negative frontotemporal dementia linked to chromosome 17
Matt Baker, Ian R Mackenzie, Stuart M Pickering-Brown, et al.
Neurobiology of Aging
|
February 17, 2009
Ubiquitin associated protein 1 is a risk factor for frontotemporal lobar degeneration
Sara Rollinson, Patrizia Rizzu, Stephen Sikkink, et al.
Communications Medicine
|
December 12, 2025
Clinical recognition of frontotemporal dementia with right temporal predominance: a consensus statement from the International Working Group
Hulya Ulugut, Kyan Younes, Maxime Montembeault, 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.
Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association
|
July 10, 2024
Clinical recognition of frontotemporal dementia with right anterior temporal predominance: A multicenter retrospective cohort study
Hulya Ulugut, Maxime Bertoux, Kyan Younes, et al.
JAMA Neurology
|
April 17, 2013
A multicenter study of glucocerebrosidase mutations in dementia with Lewy bodies
Michael A Nalls, Raquel Duran, Grisel Lopez, 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.
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of 4
Search research articles
Search
Showing results (21-30 of 34) with videos related to
Sort By:
Page
of 4
Neurobiology of Aging
|
January 18, 2015
Small deletion in C9orf72 hides a proportion of expansion carriers in FTLD
Sara Rollinson, Janis Bennion Callister, Kate Young, et al.
Neurobiology of Aging
|
June 2, 2014
Exome sequencing identifies 2 novel presenilin 1 mutations (p.L166V and p.S230R) in British early-onset Alzheimer's disease
Celeste Sassi, Rita Guerreiro, Raphael Gibbs, et al.
Parkinsonism & Related Disorders
|
October 26, 2010
Glucocerebrosidase mutations in diffuse Lewy body disease
Kenya Nishioka, Owen A Ross, Carles Vilariño-Güell, et al.
Nature
|
July 25, 2006
Mutations in progranulin cause tau-negative frontotemporal dementia linked to chromosome 17
Matt Baker, Ian R Mackenzie, Stuart M Pickering-Brown, et al.
Neurobiology of Aging
|
February 17, 2009
Ubiquitin associated protein 1 is a risk factor for frontotemporal lobar degeneration
Sara Rollinson, Patrizia Rizzu, Stephen Sikkink, et al.
Communications Medicine
|
December 12, 2025
Clinical recognition of frontotemporal dementia with right temporal predominance: a consensus statement from the International Working Group
Hulya Ulugut, Kyan Younes, Maxime Montembeault, 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.
Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association
|
July 10, 2024
Clinical recognition of frontotemporal dementia with right anterior temporal predominance: A multicenter retrospective cohort study
Hulya Ulugut, Maxime Bertoux, Kyan Younes, et al.
JAMA Neurology
|
April 17, 2013
A multicenter study of glucocerebrosidase mutations in dementia with Lewy bodies
Michael A Nalls, Raquel Duran, Grisel Lopez, 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.
Page
of 4