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Neurobiology of Aging
|
January 27, 2016
Reduced secretion and altered proteolytic processing caused by missense mutations in progranulin
Gernot Kleinberger, Anja Capell, Nathalie Brouwers, et al.
The Journals of Gerontology. Series B, Psychological Sciences and Social Sciences
|
March 24, 2007
Cholesterol and triglycerides moderate the effect of apolipoprotein E on memory functioning in older adults
Cindy M de Frias, David Bunce, Ake Wahlin, et al.
American Journal of Alzheimer'S Disease and Other Dementias
|
October 3, 2009
Novel PSEN1 mutation in a Bulgarian patient with very early-onset Alzheimer's disease, spastic paraparesis, and extrapyramidal signs
Latchezar Dintchov Traykov, Shima Mehrabian, Marleen Van den Broeck, et al.
Genome Research
|
March 3, 2005
novoSNP, a novel computational tool for sequence variation discovery
Stefan Weckx, Jurgen Del-Favero, Rosa Rademakers, et al.
Annals of Neurology
|
February 26, 2003
PRNP Val129 homozygosity increases risk for early-onset Alzheimer's disease
Bart Dermaut, Esther A Croes, Rosa Rademakers, et al.
Journal of Neurology
|
May 8, 2002
Diagnostic accuracy of the Preclinical AD Scale (PAS) in cognitively mildly impaired subjects
Pieter Jelle Visser, Frans R J Verhey, Philip Scheltens, et al.
Human Mutation
|
June 6, 2006
Mean age-of-onset of familial alzheimer disease caused by presenilin mutations correlates with both increased Abeta42 and decreased Abeta40
Samir Kumar-Singh, Jessie Theuns, Bianca Van Broeck, et al.
Neuroscience Letters
|
January 13, 2006
Reduced hippocampal volume in non-demented carriers of the apolipoprotein E epsilon4: relation to chronological age and recognition memory
Johanna Lind, Anne Larsson, Jonas Persson, et al.
Human Molecular Genetics
|
May 13, 2005
Genomic architecture of human 17q21 linked to frontotemporal dementia uncovers a highly homologous family of low-copy repeats in the tau region
Marc Cruts, Rosa Rademakers, Ilse Gijselinck, et al.
Journal of the American Geriatrics Society
|
December 2, 2004
Genetic testing has no place as a routine diagnostic test in sporadic and familial cases of Alzheimer's disease
Tischa J M van der Cammen, Esther A Croes, Bart Dermaut, et al.
Page
of 9
Search research articles
Search
Showing results (21-30 of 85) with videos related to
Sort By:
Page
of 9
Neurobiology of Aging
|
January 27, 2016
Reduced secretion and altered proteolytic processing caused by missense mutations in progranulin
Gernot Kleinberger, Anja Capell, Nathalie Brouwers, et al.
The Journals of Gerontology. Series B, Psychological Sciences and Social Sciences
|
March 24, 2007
Cholesterol and triglycerides moderate the effect of apolipoprotein E on memory functioning in older adults
Cindy M de Frias, David Bunce, Ake Wahlin, et al.
American Journal of Alzheimer'S Disease and Other Dementias
|
October 3, 2009
Novel PSEN1 mutation in a Bulgarian patient with very early-onset Alzheimer's disease, spastic paraparesis, and extrapyramidal signs
Latchezar Dintchov Traykov, Shima Mehrabian, Marleen Van den Broeck, et al.
Genome Research
|
March 3, 2005
novoSNP, a novel computational tool for sequence variation discovery
Stefan Weckx, Jurgen Del-Favero, Rosa Rademakers, et al.
Annals of Neurology
|
February 26, 2003
PRNP Val129 homozygosity increases risk for early-onset Alzheimer's disease
Bart Dermaut, Esther A Croes, Rosa Rademakers, et al.
Journal of Neurology
|
May 8, 2002
Diagnostic accuracy of the Preclinical AD Scale (PAS) in cognitively mildly impaired subjects
Pieter Jelle Visser, Frans R J Verhey, Philip Scheltens, et al.
Human Mutation
|
June 6, 2006
Mean age-of-onset of familial alzheimer disease caused by presenilin mutations correlates with both increased Abeta42 and decreased Abeta40
Samir Kumar-Singh, Jessie Theuns, Bianca Van Broeck, et al.
Neuroscience Letters
|
January 13, 2006
Reduced hippocampal volume in non-demented carriers of the apolipoprotein E epsilon4: relation to chronological age and recognition memory
Johanna Lind, Anne Larsson, Jonas Persson, et al.
Human Molecular Genetics
|
May 13, 2005
Genomic architecture of human 17q21 linked to frontotemporal dementia uncovers a highly homologous family of low-copy repeats in the tau region
Marc Cruts, Rosa Rademakers, Ilse Gijselinck, et al.
Journal of the American Geriatrics Society
|
December 2, 2004
Genetic testing has no place as a routine diagnostic test in sporadic and familial cases of Alzheimer's disease
Tischa J M van der Cammen, Esther A Croes, Bart Dermaut, et al.
Page
of 9