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Neurology
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January 29, 2003
Early onset familial Alzheimer's disease: Mutation frequency in 31 families
J C Janssen, J A Beck, T A Campbell, et al.
Human Mutation
|
March 25, 1999
Pathogenic presenilin 1 mutations (P436S & I143F) in early-onset Alzheimer's disease in the UK. Mutations in brief no. 223. Online
M S Palmer, J A Beck, T A Campbell, et al.
Neuroscience Letters
|
August 19, 1983
Loss of pigmented dopamine-beta-hydroxylase positive cells from locus coeruleus in senile dementia of Alzheimer's type
L L Iversen, M N Rossor, G P Reynolds, et al.
The American Journal of Pathology
|
April 1, 1996
Predominant deposition of amyloid-beta 42(43) in plaques in cases of Alzheimer's disease and hereditary cerebral hemorrhage associated with mutations in the amyloid precursor protein gene
D M Mann, T Iwatsubo, Y Ihara, et al.
Nature
|
December 8, 1983
Neuropeptide Y distribution in human brain
T E Adrian, J M Allen, S R Bloom, et al.
Neurology
|
May 29, 2001
Progressive brain atrophy on serial MRI in dementia with Lewy bodies, AD, and vascular dementia
J T O'Brien, S Paling, R Barber, et al.
Neurology
|
October 29, 2008
Tracking progression in frontotemporal lobar degeneration: serial MRI in semantic dementia
J D Rohrer, E McNaught, J Foster, et al.
The British Journal of Psychiatry : the Journal of Mental Science
|
April 1, 1991
Evidence for allelic heterogeneity in familial early-onset Alzheimer's disease
C M van Duijn, C van Broeckhoven, J A Hardy, et al.
Brain : a Journal of Neurology
|
February 1, 1995
Chromosome 14 linked familial Alzheimer's disease. A clinico-pathological study of a single pedigree
A M Kennedy, S K Newman, R S Frackowiak, et al.
Annals of Neurology
|
April 20, 2001
Patterns of temporal lobe atrophy in semantic dementia and Alzheimer's disease
D Chan, N C Fox, R I Scahill, et al.
Page
of 22
Search research articles
Search
Showing results (181-190 of 216) with videos related to
Sort By:
Page
of 22
Neurology
|
January 29, 2003
Early onset familial Alzheimer's disease: Mutation frequency in 31 families
J C Janssen, J A Beck, T A Campbell, et al.
Human Mutation
|
March 25, 1999
Pathogenic presenilin 1 mutations (P436S & I143F) in early-onset Alzheimer's disease in the UK. Mutations in brief no. 223. Online
M S Palmer, J A Beck, T A Campbell, et al.
Neuroscience Letters
|
August 19, 1983
Loss of pigmented dopamine-beta-hydroxylase positive cells from locus coeruleus in senile dementia of Alzheimer's type
L L Iversen, M N Rossor, G P Reynolds, et al.
The American Journal of Pathology
|
April 1, 1996
Predominant deposition of amyloid-beta 42(43) in plaques in cases of Alzheimer's disease and hereditary cerebral hemorrhage associated with mutations in the amyloid precursor protein gene
D M Mann, T Iwatsubo, Y Ihara, et al.
Nature
|
December 8, 1983
Neuropeptide Y distribution in human brain
T E Adrian, J M Allen, S R Bloom, et al.
Neurology
|
May 29, 2001
Progressive brain atrophy on serial MRI in dementia with Lewy bodies, AD, and vascular dementia
J T O'Brien, S Paling, R Barber, et al.
Neurology
|
October 29, 2008
Tracking progression in frontotemporal lobar degeneration: serial MRI in semantic dementia
J D Rohrer, E McNaught, J Foster, et al.
The British Journal of Psychiatry : the Journal of Mental Science
|
April 1, 1991
Evidence for allelic heterogeneity in familial early-onset Alzheimer's disease
C M van Duijn, C van Broeckhoven, J A Hardy, et al.
Brain : a Journal of Neurology
|
February 1, 1995
Chromosome 14 linked familial Alzheimer's disease. A clinico-pathological study of a single pedigree
A M Kennedy, S K Newman, R S Frackowiak, et al.
Annals of Neurology
|
April 20, 2001
Patterns of temporal lobe atrophy in semantic dementia and Alzheimer's disease
D Chan, N C Fox, R I Scahill, et al.
Page
of 22