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Brain : a Journal of Neurology
|
August 22, 2006
APP duplication is sufficient to cause early onset Alzheimer's dementia with cerebral amyloid angiopathy
Kristel Sleegers, Nathalie Brouwers, Ilse Gijselinck, et al.
Brain : a Journal of Neurology
|
March 16, 2006
Reduced functional brain activity response in cognitively intact apolipoprotein E epsilon4 carriers
Johanna Lind, Jonas Persson, Martin Ingvar, et al.
Acta Neuropathologica
|
August 15, 2012
The genetics and neuropathology of frontotemporal lobar degeneration
Anne Sieben, Tim Van Langenhove, Sebastiaan Engelborghs, et al.
Journal of Neuropathology and Experimental Neurology
|
May 3, 2006
Characterization of ubiquitinated intraneuronal inclusions in a novel Belgian frontotemporal lobar degeneration family
Daniel Pirici, Rik Vandenberghe, Rosa Rademakers, et al.
Science (New York, N.Y.)
|
February 9, 2013
The C9orf72 GGGGCC repeat is translated into aggregating dipeptide-repeat proteins in FTLD/ALS
Kohji Mori, Shih-Ming Weng, Thomas Arzberger, et al.
Annals of Neurology
|
August 2, 2003
Early cognitive decline is associated with prion protein codon 129 polymorphism
Esther A Croes, Bart Dermaut, Jeanine J Houwing-Duistermaat, et al.
Neurobiology of Aging
|
July 24, 2012
Genetic association of CR1 with Alzheimer's disease: a tentative disease mechanism
Lili-Naz Hazrati, Caroline Van Cauwenberghe, Patricia L Brooks, et al.
Acta Neuropathologica Communications
|
November 21, 2013
Promoter DNA methylation regulates progranulin expression and is altered in FTLD
Julia Banzhaf-Strathmann, Rainer Claus, Oliver Mücke, et al.
American Journal of Human Genetics
|
May 7, 2002
The gene encoding nicastrin, a major gamma-secretase component, modifies risk for familial early-onset Alzheimer disease in a Dutch population-based sample
Bart Dermaut, Jessie Theuns, Kristel Sleegers, et al.
Molecular Neurodegeneration
|
July 17, 2015
Reduced secreted clusterin as a mechanism for Alzheimer-associated CLU mutations
Karolien Bettens, Steven Vermeulen, Caroline Van Cauwenberghe, et al.
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of 9
Search research articles
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Showing results (31-40 of 85) with videos related to
Sort By:
Page
of 9
Brain : a Journal of Neurology
|
August 22, 2006
APP duplication is sufficient to cause early onset Alzheimer's dementia with cerebral amyloid angiopathy
Kristel Sleegers, Nathalie Brouwers, Ilse Gijselinck, et al.
Brain : a Journal of Neurology
|
March 16, 2006
Reduced functional brain activity response in cognitively intact apolipoprotein E epsilon4 carriers
Johanna Lind, Jonas Persson, Martin Ingvar, et al.
Acta Neuropathologica
|
August 15, 2012
The genetics and neuropathology of frontotemporal lobar degeneration
Anne Sieben, Tim Van Langenhove, Sebastiaan Engelborghs, et al.
Journal of Neuropathology and Experimental Neurology
|
May 3, 2006
Characterization of ubiquitinated intraneuronal inclusions in a novel Belgian frontotemporal lobar degeneration family
Daniel Pirici, Rik Vandenberghe, Rosa Rademakers, et al.
Science (New York, N.Y.)
|
February 9, 2013
The C9orf72 GGGGCC repeat is translated into aggregating dipeptide-repeat proteins in FTLD/ALS
Kohji Mori, Shih-Ming Weng, Thomas Arzberger, et al.
Annals of Neurology
|
August 2, 2003
Early cognitive decline is associated with prion protein codon 129 polymorphism
Esther A Croes, Bart Dermaut, Jeanine J Houwing-Duistermaat, et al.
Neurobiology of Aging
|
July 24, 2012
Genetic association of CR1 with Alzheimer's disease: a tentative disease mechanism
Lili-Naz Hazrati, Caroline Van Cauwenberghe, Patricia L Brooks, et al.
Acta Neuropathologica Communications
|
November 21, 2013
Promoter DNA methylation regulates progranulin expression and is altered in FTLD
Julia Banzhaf-Strathmann, Rainer Claus, Oliver Mücke, et al.
American Journal of Human Genetics
|
May 7, 2002
The gene encoding nicastrin, a major gamma-secretase component, modifies risk for familial early-onset Alzheimer disease in a Dutch population-based sample
Bart Dermaut, Jessie Theuns, Kristel Sleegers, et al.
Molecular Neurodegeneration
|
July 17, 2015
Reduced secreted clusterin as a mechanism for Alzheimer-associated CLU mutations
Karolien Bettens, Steven Vermeulen, Caroline Van Cauwenberghe, et al.
Page
of 9